1,107 results on '"Melville, R."'
Search Results
152. The Measurement of Assimilation and Translocation in Tomato Seedlings under the Conditions of Glasshouse Culture
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BOLAS, B. D., MELVILLE, R., and SELMAN, I. W.
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- 1938
153. The Influence of Environment on the Growth and Metabolism of the Tomato Plant: I. Methods, Technique, and Preliminary Results
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BOLAS, B. D. and MELVILLE, R.
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- 1933
154. The Use and Forms of Judicial Torture in England and Scotland
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Melville, R. D.
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- 1905
155. Mortality related to actigraphic long and short sleep
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Robert Langer, Katharine M. Rex, Daniel F. Kripke, Jeffrey A. Elliott, and Melville R. Klauber
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Gerontology ,Pediatrics ,medicine.medical_specialty ,Time Factors ,Multivariate analysis ,Article ,Melatonin ,Risk Factors ,Epidemiology ,Humans ,Medicine ,Prospective Studies ,Mortality ,Prospective cohort study ,Aged ,Proportional Hazards Models ,Short sleep ,business.industry ,Proportional hazards model ,Actigraphy ,General Medicine ,Sleep in non-human animals ,Multivariate Analysis ,Female ,Sleep ,business ,medicine.drug - Abstract
The folk belief that we should sleep 8 h seems to be incorrect. Numerous studies have shown that self-reported sleep longer than 7.5 h or shorter than 6.5 h predicts increased mortality risk. This study examined if prospectively-determined objective sleep duration, as estimated by wrist actigraphy, was associated with mortality risks.From 1995-1999, women averaging 67.6 years of age provided one-week actigraphic recordings. Survival could be estimated from follow-up continuing until 2009 for 444 of the women, with an average of 10.5 years before censoring. Multivariate age-stratified Cox regression models were controlled for history of hypertension, diabetes, myocardial infarction, cancer, and major depression.Adjusted survival functions estimated 61% survival (54-69%, 95% C.I.) for those with sleep less than 300 min and 78% survival (73-85%, 95% C.I.) for those with actigraphic sleep longer than 390 min, as compared with survival of 90% (85-94%, 95% C.I.) for those with sleep of 300-390 min. Time-in-bed, sleep efficiency and the timing of melatonin metabolite excretion were also significant mortality risk factors.This study confirms a U-shaped relationship between survival and actigraphically measured sleep durations, with the optimal objective sleep duration being shorter than the self-report optimums. People who sleep five or six hours may be reassured. Further studies are needed to identify any modifiable factors for this mortality and possible approaches to prevention.
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- 2011
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156. Neurological findings in Alzheimer's disease and normal aging
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Galasko, Douglas, Kwo-on-Yuen, Pow F., Klauber, Melville R., and Thal, Leon J.
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Aging -- Physiological aspects ,Alzheimer's disease -- Diagnosis ,Alzheimer's disease -- Physiological aspects ,Health - Abstract
People with Alzheimer's disease (AD) are often found to have other neurological problems such as primitive reflexes (motion patterns usually found in infants), impaired sensory perception (such as difficulty recognizing what the hand is grasping), and altered muscle function and walking patterns. Some attempts to classify subtypes of AD have made use of these abnormalities. Previous studies of the neurological dysfunctions have been hampered by lack of proper controls, that is, nondemented elderly individuals in whom some deterioration of nervous function is normally anticipated. Secondly, previous studies have focused on patients late in the course of AD, many of whom were in nursing homes. The current study has focused on a relatively large group of 135 individuals with mild to moderate AD who were compared with a similarly sized group of elderly control subjects. The AD group was an average of three years older and had an average of two years less education than the control group. Neurological data were corrected for these differences. The AD group had significantly more rigidity, stooped posture, impaired graphesthesia (recognition of numbers, words, etc. when traced on the skin), impaired face-hand test (to measure attention to simultaneous tactile stimuli), and more primitive reflexes. Abnormalities in gait (walking pattern) and muscle movement (cogwheeling, a Parkinsonian type of movement), and immobile facial muscles were also frequent in the AD group, although not significantly so. Only a few of these signs increased as AD became more severe. Primitive reflexes and altered motor findings do not reliably distinguish mild AD from normal aging, but graphesthesia and the face-hand test may complement mental status tests in supporting an AD diagnosis. The grasp reflex also increased with AD severity. Long-term follow-up of the AD subjects may be needed to determine if the Parkinsonian-like movement disorders indicated a subset of AD. (Consumer Summary produced by Reliance Medical Information, Inc.)
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- 1990
157. Comment on proposals for the amendment of Opinion 610 (family-group names based on generic names having the stem Drepan-). Z.N.(S.) 1958
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Melville, R V and BioStor
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- 1974
158. TORNATELLINA MOLLUSCA GASTROPODA PROPOSED DIRECTION TO COMPLETE A RULING IN OPINION 119
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Melville, R V and BioStor
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- 1985
159. Galaxias platei Steindachner 1899 (Pisces, Galaxiidae): revised proposal to give precedence over Galaxias delfrni Philippi, 1895. Z.N.(S.) 1877
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Melville, R V and BioStor
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- 1977
160. Death of a member of the Commission
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Melville, R V and BioStor
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- 1977
161. Special announcement. Financial help for the Commission
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Melville, R V and BioStor
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- 1977
162. Spectroscopic studies of β-cyclodextrin-complexed cyanine dyes
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Erin Denise Moritz and Melville R. V. Sahyun
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Absorption spectroscopy ,General Chemical Engineering ,Dimer ,General Physics and Astronomy ,Hyperpolarizability ,General Chemistry ,Photochemistry ,Photoexcitation ,chemistry.chemical_compound ,Homologous series ,Monomer ,chemistry ,Excited state ,Cyanine - Abstract
We have studied the interaction of a homologous series of symmetrical thiacyanine dyes (DTCI, DTDCI, DTTCI) with β-cyclodextrin. From absorption spectra we infer that all three dyes form β-CD complexes, either as dye cation monomer or dimer. Higher aggregates, e.g. H-aggregates, are observable in water alone for both DTDCI and DTTCI, as is well-known. The H-aggregate formed from DTTCI in water provides evidence of a unique pathway for thermalization of photoexcitation energy; excited aggregate ejects excited dye monomer. β-CD complexes of all three dyes exhibit technologically useful levels of second-order hyperpolarizability, measured by Hyper-Rayleigh scattering, and we assign the non-linear optical response to dimer complex. Second-order scattering is observed, however, only when the saturation concentration of dye monomer in water is exceeded; at lower concentrations we infer that complexes do not form. Computational modelling, carried out for DTCI, suggests that the dimer forms endergonically with a structure that both locks in a significant degree of bond alternation, as well as allowing considerable freedom for torsional relaxation.
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- 2005
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163. Comments on the proposed validation of Ammonites laevigatas J. de C. Sowerby, 1827, in two distinct senses
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Melville, R V, Casey, R, and BioStor
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- 1962
164. Comment on the proposed suppression of Amphisbaena mildei Peters, 1878. Z.N.(S.) 1746
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Melville, R V and BioStor
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- 1969
165. Sensitization of photoeffects by hyper-Rayleigh scattering (HRS)
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Matthew Goertz and Melville R. V. Sahyun
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Absorption spectroscopy ,Chemistry ,Scattering ,General Chemical Engineering ,Analytical chemistry ,General Physics and Astronomy ,General Chemistry ,Molecular physics ,Fluorescence ,Light scattering ,Fluorescence spectroscopy ,symbols.namesake ,Resonance fluorescence ,Excited state ,symbols ,Rayleigh scattering - Abstract
We have observed fluorescence from Coumarin334 (C334) in a variety of solvents using a fundamental wavelength (840 nm) twice that of radiation actinic for excitation of this fluorescence, and we attribute this fluorescence to second harmonic, hyper-Rayleigh light scattering (HRS). Fluorescence intensity is compared to that obtained by direct excitation of fluorescence under the same conditions to provide an estimate of the efficiency of the HRS process; Φ= ca . 10 −6 , strongly solvent dependent. Photochemical actinometry indicates a fundamental optical power of 1 mW cm−2 under our conditions. By mapping the action spectrum for second harmonic excitation of fluorescence, we exclude the possibility suggested by the solvent dependence of Φ, namely that the principal pathway for excitation of C334 involves second harmonic scattering by solvent, followed by absorption of actinic light by the solute. Instead, we find that the action spectrum does not correlate with the absorption spectrum of C334. Therefore, we hypothesize that second harmonic scattering is coupled to an electronic transition in the C334 chromophore, which probably involves a higher excited state than that responsible for emission.
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- 2003
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166. Melatonin excretion with affect disorders over age 60
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Katharine M. Rex, Shawn D. Youngstedt, Jeffrey A. Elliott, Daniel F. Kripke, and Melville R. Klauber
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Male ,Senescence ,Sleep disorder ,medicine.medical_specialty ,Mood Disorders ,Neurological disorder ,Middle Aged ,medicine.disease ,Circadian Rhythm ,Excretion ,Melatonin ,Psychiatry and Mental health ,Mood ,Endocrinology ,Internal medicine ,medicine ,Humans ,Female ,Circadian rhythm ,Psychology ,Biological Psychiatry ,Depression (differential diagnoses) ,Aged ,medicine.drug - Abstract
Numerous studies have reported low melatonin secretion in depression, but other studies have suggested no deficit or an increase. Alterations of circadian phase or duration of melatonin secretion have also been described. Since melatonin secretion decreases as we age, it seemed interesting to examine melatonin and depression in an aging sample. Volunteers who complained of mood or sleep problems were recruited for studies in which fractional urine specimens were collected for 24 h, both at home and in the laboratory. The major metabolite, 6-sulfatoxymelatonin (aMT6s), was determined by radioimmunoassay. Of 72 volunteers aged 60-78 years, seven had current major depression and 55% had a lifetime history of an affective disorder. A 55-fold range of home aMT6s excretion rates was observed. A lifetime history of any affective disorder was significantly associated with greater log(10)[mesor] aMT6s excretion in home collections and laboratory collections, but current affective disorders were neither significantly related to melatonin excretion nor to aMT6s acrophase timing, onset, offset or duration. These results are only weakly consistent with a photoperiodic hypothesis of depression.
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- 2003
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167. Light therapy of late luteal phase dysphoric disorder: an extended study
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Parry, Barbara L., Mahan, Anne M., Mostofi, Nasim, Klauber, Melville R., Lew, Gavin S., and Gillin, J. Christian
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Depression, Mental -- Care and treatment ,Premenstrual syndrome -- Care and treatment ,Phototherapy -- Psychological aspects ,Health ,Psychology and mental health - Abstract
Nineteen patients with late luteal phase dysphoric disorder (LLPDD) and 11 healthy comparison subjects underwent a 3-month crossover trial of bright (more than 2500 lux) white morning, bright white evening, and placebo dim (less than 10 lux) red evening light, administered daily for 1 week during the premenstrual phase of the menstrual cycle. All light treatments significantly reduced depressive ratings from baseline levels.
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- 1993
168. Depression and endogenous melatonin in postmenopausal women
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Daniel F. Kripke, Melville R. Klauber, Katharine M. Rex, Jeffrey A. Elliott, Joseph D Assmus, Arja Tuunainen, and Robert Langer
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medicine.medical_specialty ,Urinary system ,Global Assessment of Functioning ,Physiology ,Melatonin ,Excretion ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,Humans ,Circadian rhythm ,Family history ,Depression (differential diagnoses) ,Aged ,Aged, 80 and over ,Depressive Disorder ,Depressive Disorder, Major ,Mood Disorders ,Middle Aged ,medicine.disease ,030227 psychiatry ,3. Good health ,Psychiatry and Mental health ,Clinical Psychology ,Endocrinology ,Mood disorders ,Female ,Psychology ,030217 neurology & neurosurgery ,medicine.drug - Abstract
Background: Previous reports on melatonin secretion in depression are numerous but conflicting. There are very few studies relating the duration of the nocturnal melatonin peak to depression, and the results of those studies have been equivocal. Methods: We studied mood disorders and urinary melatonin excretion in 382 postmenopausal women. Psychiatric diagnoses and global assessment of functioning (GAF) scores were determined based on a Structured Clinical Interview for DSM-IV Axis I Disorders (SCID). Urinary 6-sulfatoxymelatonin (6-SMT) samples were collected for two 24-h periods at home. Results: A positive family history of depression was significantly related to a longer duration of 6-SMT excretion. There were marginally significant associations between current major depression and delayed offset of 6-SMT excretion and between later acrophase and lifetime major depression, even with control for age, ethnicity, season, and several medications. Limitations: The subjects were studied in their home environments, where light effects were not controlled. Data were restricted to postmenopausal women, including a limited number of subjects with current major depression. Conclusions: These results suggest that there might be a familial vulnerability in the endogenous melatonin signal in subjects prone to depression, and an abnormality in the duration of the melatonin signal in those with current major depression.
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- 2002
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169. The Savior in Kirtland Karl Ricks Anderson
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Melville, R. Mark
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- 2013
170. A Firm Foundation: Church Organization and Administration David J. Whittaker Arnold K. Garr
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Melville, R. Mark
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- 2013
171. No Weapon Shall Prosper: New Light on Sensitive Issues Robert L. Millet
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Melville, R. Mark
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- 2013
172. Opportunistic infections and AIDS malignancies early after initiating combination antiretroviral therapy in high-income countries
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Lodi, Sara, Del Amo, Julia, Moreno, Santiago, Bucher, H. C., Furrer, Hansjakob, Logan, Roger, Sterne, Jonathan, Pérez-Hoyos, Santiago, Jarrín, Inma, Phillips, Andrew, Olson, Ashley, Van Sighem, Ard, Reiss, Peter, Sabin, C., Jose, Sophie, Justice, Amy, Goulet, Joseph, Miró, José M., Ferrer, Elena, Meyer, Laurence, Seng, Rémonie, Vourli, Georgia, Antoniadou, Anastasia, Dabis, Francois, Vandenhede, Mari Anne, Costagliola, Dominique, Abgrall, S., Hernán, Miguel A., Hernan, Miguel, Bansi, L., Hill, T., Dunn, D., Porter, K., Glabay, A., Orkin, C., Thomas, R., Jones, K., Fisher, M., Perry, N., Pullin, A., Churchill, D., Gazzard, B., Nelson, M., Asboe, D., Bulbeck, S., Mandalia, S., Clarke, J., Delpech, V., Anderson, J., Munshi, S., Post, F., Easterbrook, P., Khan, Y., Patel, P., Karim, F., Duffell, S., Gilson, R., Man, S. L., Williams, I., Gompels, M., Dooley, D., Schwenk, A., Ainsworth, J., Johnson, M., Youle, M., Lampe, F., Smith, C., Grabowska, H., Chaloner, C., Ismajani Puradiredja, D., Phillips, A., Walsh, J., Weber, J., Kemble, C., Mackie, N., Winston, A., Leen, C., Wilson, A., Bezemer, D. O., Gras, L. A.J., Kesselring, A. M., Van Sighem, A. I., Zaheri, S., Van Twillert, G., Kortmann, W., Branger, J., Prins, J. M., Kuijpers, T. W., Scherpbier, H. J., Van Der Meer, J. T.M., Wit, F. W.M.N., Godfried, M. H., Reiss, P., Van Der Poll, T., Nellen, F. J.B., Lange, J. M.A., Geerlings, S. E., Van Vugt, M., Pajkrt, D., Bos, J. C., Van Der Valk, M., Grijsen, M. L., Wiersinga, W. J., Brinkman, K., Blok, W. L., Frissen, P. H.J., Schouten, W. E.M., Van Den Berk, G. E.L., Veenstra, J., Lettinga, K. D., Mulder, J. W., Vrouenraets, S. M.E., Lauw, F. N., Van Eeden, A., Verhagen, D. W.M., Van Agtmael, M. A., Perenboom, R. M., Claessen, F. A.P., Bomers, M., Peters, E. J.G., Richter, C., Van Der Berg, J. P., Gisolf, E. H., Schippers, E. F., Van Nieuwkoop, C., Van Elzakker, E. P., Leyten, E. M.S., Gelinck, L. B.S., Pronk, M. J.H., Bravenboer, B., Kootstra, G. J., Delsing, C. E., Sprenger, H. G., Doedens, R., Scholvinck, E. H., Van Assen, S., Bierman, W. F.W., Soetekouw, R., Ten Kate, R. W., Van Vonderen, M. G.A., Van Houte, D. P.F., Kroon, F. P., Van Dissel, J. T., Arend, S. M., De Boer, M. G.J., Jolink, H., Ter Vollaard, H. J.M., Bauer, M. P., Weijer, S., El Moussaoui, R., Lowe, S., Schreij, G., Oude Lashof, A., Posthouwer, D., Koopmans, P. P., Keuter, M., Van Der Ven, A. J.A.M., Ter Hofstede, H. J.M., Dofferhoff, A. S.M., Warris, A., Van Crevel, R., Van Der Ende, M. E., De Vries-Sluijs, T. E.M.S., Schurink, C. A.M., Nouwen, J. L., Nispen Tot Pannerden, M. H., Verbon, A., Rijnders, B. J.A., Van Gorp, E. C.M., Hassing, R. J., Smeulders, A. W.M., Hartwig, N. G., Driessen, G. J.A., Den Hollander, J. G., Pogany, K., Juttmann, J. R., Van Kasteren, M. E.E., Hoepelman, A. I.M., Mudrikova, T., Schneider, M. M.E., Jaspers, C. A.J.J., Ellerbroek, P. M., Oosterheert, J. J., Arends, J. E., Wassenberg, M. W.M., Barth, R. E., Geelen, S. P.M., Wolfs, T. F.W., Bont, L. J., Van Den Berge, M., Stegeman, A., Groeneveld, P. H.P., Alleman, M. A., Bouwhuis, J. W., Barin, F., Burty, C., Duvivier, C., Enel, P., Fredouille-Heripret, L., Gasnault, J., Khuong, M. A., Mahamat, A., Pilorgé, F., Tattevin, P., Salomon, Valérie, Jacquemet, N., Costagliola, D., Grabar, S., Guiguet, M., Lanoy, E., Lièvre, L., Mary-Krause, M., Selinger-Leneman, H., Lacombe, J. M., Potard, V., Bricaire, F., Herson, S., Katlama, C., Simon, A., Desplanque, N., Girard, P. M., Meynard, J. L., Meyohas, M. C., Picard, O., Cadranel, J., Mayaud, C., Pialoux, G., Clauvel, J. P., Decazes, J. M., Gérard, L., Molina, J. M., Diemer, M., Sellier, P., Bentata, M., Honoré, P., Jeantils, V., Tassi, S., Mechali, D., Taverne, B., Bouvet, E., Crickx, B., Ecobichon, J. L., Matheron, S., Picard-Dahan, C., Yeni, P., Berthé, H., Dupont, C., Chandemerle, C., Mortier, E., De Truchis, P., Tisne-Dessus, D., Weiss, L., Salmon, D., Auperin, I., Gilquin, J., Roudière, L., Viard, J. P., Boue, F., Fior, R., Delfraissy, J. F., Goujard, C., Jung, C., Lesprit, Ph, Vittecoq, D., Fraisse, P., Lang, J. M., Rey, D., Beck-Wirth, G., Stahl, J. P., Lecercq, P., Gourdon, F., Laurichesse, H., Fresard, A., Lucht, F., Bazin, C., Verdon, R., Chavanet, P., Arvieux, C., Michelet, C., Choutet, P., Goudeau, A., Maître, M. F., Hoen, B., Eglinger, P., Faller, J. P., Borsa-Lebas, F., Caron, F., Reynes, J., Daures, J. P., May, T., Rabaud, C., Berger, J. L., Rémy, G., Arlet-Suau, E., Cuzin, L., Massip, P., Thiercelin Legrand, M. F., Pontonnier, G., Viget, N., Yasdanpanah, Y., Dellamonica, P., Pradier, C., Pugliese, P., Aleksandrowicz, K., Quinsat, D., Ravaux, I., Tissot-Dupont, H., Delmont, J. P., Moreau, J., Gastaut, J. A., Poizot Martin, I., Retornaz, F., Soubeyrand, J., Galinier, A., Ruiz, J. M., Allegre, T., Blanc, P. A., Bonnet-Montchardon, D., Lepeu, G., Granet-Brunello, P., Esterni, J. P., Pelissier, L., Cohen-Valensi, R., Nezri, M., Chadapaud, S., Laffeuillade, A., Billaud, E., Raffi, F., Boibieux, A., Peyramond, D., Livrozet, J. M., Touraine, J. L., Cotte, L., Trepo, C., Strobel, M., Bissuel, F., Pradinaud, R., Sobesky, M., Cabié, A., Gaud, C., Contant, M., Aubert, V., Barth, J., Battegay, M., Bernasconi, E., Böni, J., Burton-Jeangros, C., Calmy, A., Cavassini, M., Egger, M., Elzi, L., Fehr, J., Fellay, J., Furrer, H., Haerry, D., Fux, C. A., Gorgievski, M., Günthard, H., Hasse, B., Hirsch, H. H., Hösli, I., Kahlert, C., Kaiser, L., Keiser, O., Klimkait, T., Kovari, H., Ledergerber, B., Martinetti, G., Martinez De Tejada, B., Metzner, K., Müller, N., Nadal, D., Pantaleo, G., Rauch, A., Regenass, S., Rickenbach, M., Rudin, C., Schmid, P., Schultze, D., Schöni-Affolter, F., Schüpbach, J., Speck, R., Taffé, P., Tarr, P., Telenti, A., Trkola, A., Vernazza, P., Weber, R., Yerly, S., Casabona, J., Gallois, A., Esteve, A., Podzamczer, D., Murillas, J., Gatell, J. M., Manzardo, C., Tural, C., Clotet, B., Ferrer, E., Riera, M., Segura, F., Navarro, G., Force, L., Vilaró, J., Masabeu, A., García, I., Guadarrama, M., Cifuentes, C., Dalmau, D., Jaen, Agustí, C., Montoliu, A., Pérez, I., Gargoulas, Freyra, Blanco, J. L., Garcia-Alcaide, F., Martínez, E., Mallolas, J., López-Dieguez, M., García-Goez, J. F., Sirera, G., Romeu, J., Jou, A., Negredo, E., Miranda, C., Capitan, M. C., Saumoy, M., Imaz, A., Tiraboschi, J. M., Murillo, O., Bolao, F., Peña, C., Cabellos, C., Masó, M., Vila, A., Sala, M., Cervantes, M., Jose Amengual, Ma, Navarro, M., Penelo, E., Barrufet, P., Bejarano, G., Molina, J., Alvaro, M., Mercadal, J., Fernandez, Juanse, Ospina, Jesus E., Muñoz, M. A., Caro-Murillo, A. M., Sobrino, P., Jarrín, I., Gomez Sirvent, J. L., Rodríguez, P., Aleman, M. R., Alonso, M. M., Lopez, A. M., Hernandez, M. I., Soriano, V., Labarga, P., Barreiro, P., Medrano, J., Rivas, P., Herrero, D., Blanco, F., Vispo, M. E., Martín, L., Ramírez, G., De Diego, M., Rubio, R., Pulido, F., Moreno, V., Cepeda, C., Hervás, Rl, Iribarren, J. A., Arrizabalaga, J., Aramburu, M. J., Camino, X., Rodrí-guez-Arrondo, F., Von Wichmann, M. A., Pascual, L., Goenaga, M. A., Gutierrez, F., Masia, M., Ramos, J. M., Padilla, S., Sanchez-Hellín, V., Bernal, E., Escolano, C., Montolio, F., Peral, Y., Berenguer, J., Lopez, J. C., Miralles, P., Cosín, J., Sanchez, M., Gutierrez, I., Ramírez, M., Padilla, B., Vidal, F., Sanjuan, M., Peraire, J., Veloso, S., Vilades, C., Lopez-Dupla, M., Olona, M., Vargas, M., Aldeguer, J. L., Blanes, M., Lacruz, J., Salavert, M., Montero, M., Cuéllar, S., De Los Santos, I., Sanz, J., Oteo, J. A., Blanco, J. R., Ibarra, V., Metola, L., Sanz, M., Pérez-Martínez, L., Sola, J., Uriz, J., Castiello, J., Reparaz, J., Arriaza, M. J., Irigoyen, C., Moreno, S., Antela, A., Casado, J. L., Dronda, F., Moreno, A., Pérez, M. J., López, D., Gutiérrez, C., Hernández, B., Pumares, M., Martí, P., García, L., Page, C., García, F., Hernández, J., Peña, A., Muñoz, L., Parra, J., Viciana, P., Leal, M., López-Cortés, L. F., Trastoy, M., Mata, R., Justice, A. C., Fiellin, D. A., Rimland, D., Jones-Taylor, C., Oursler, K. A., Titanji, R., Brown, S., Garrison, S., Rodriguez-Barradas, M., Masozera, N., Goetz, M., Leaf, D., Simberkoff, M., Blumenthal, D., Leung, J., Butt, A., Hoffman, E., Gibert, C., Peck, R., Mattocks, K., Braithwaite, S., Brandt, C., Bryant, K., Cook, R., Conigliaro, J., Crothers, K., Chang, J., Crystal, S., Day, N., Erdos, J., Freiberg, M., Kozal, M., Gandhi, N., Gaziano, M., Gerschenson, M., Good, B., Gordon, A., Goulet, J. L., Hernán, M. A., Kraemer, K., Lim, J., Maisto, S., Miller, P., Mole, L., O'Connor, P., Papas, R., Robins, J. M., Rinaldo, C., Roberts, M., Samet, J., Tierney, B., Whittle, J., Babiker, A., Brettle, R., Darbyshire, J., Goldberg, D., Hawkins, D., Jaffe, H., Johnson, A., McLean, K., Pillay, D., Cursley, Adam, Ewings, Fiona, Fairbrother, Keith, Louisa Gnatiuc, S. L., Murphy, Brendan, Douglas, G., Kennedy, N., Pritchard, J., Andrady, U., Rajda, N., Maw, R., McKernan, S., Drake, S., Gilleran, G., White, D., Ross, J., Toomer, S., Hewart, R., Wilding, H., Woodward, R., Dean, G., Heald, L., Horner, P., Glover, S., Bansaal, D., Eduards, S., Carne, C., Browing, M., Das, R., Stanley, B., Estreich, S., Magdy, A., O'Mahony, C., Fraser, P., Hayman, B., Jebakumar, S. P.R., Joshi, U., Ralph, S., Wade, A., Mette, R., Lalik, J., Summerfield, H., El-Dalil, A., France, J. A., White, C., Robertson, R., Gordon, S., McMillan, S., Morris, S., Lean, C., Vithayathil, K., McLean, L., Winter, A., Gale, D., Jacobs, S., Tayal, S., Short, L., Green, S., Williams, G., Sivakumar, K., Bhattacharyya, N. D., Monteiro, E., Minton, J., Dhar, J., Nye, F., De Souza, C. B., Isaksen, A., McDonald, L., Franca, A., William, L., Jendrulek, I., Peters, B., Shaunak, S., El-Gadi, S., Easterbrook, P. J., Mazhude, C., Johnstone, R., Fakoya, A., McHale, J., Waters, A., Kegg, S., Mitchell, S., Byrne, P., Rice, P., Fidler, S., Mullaney, S. A., McCormack, S., David, D., Melville, R., Phillip, K., Balachandran, T., Mabey-Puttock, S., Sukthankar, A., Murphy, C., Wilkins, E., Ahmad, S., Haynes, J., Evans, E., Ong, E., Grey, R., Meaden, J., Bignell, C., Loay, D., Peacock, K., Girgis, M. R., Morgan, B., Palfreeman, A., Wilcox, J., Tobin, J., Tucker, L., Saeed, A. M., Chen, F., Deheragada, A., Williams, O., Lacey, H., Herman, S., Kinghorn, D., Devendra, V. 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A., Guerrero, R., Rivera, E., Marco, A., Quintana, M., Gonzalez, C., Castilla, J., Guevara, M., De Mendoza, C., Zahonero, N., Ortíz, M., Paraskevis, D., Touloumi, G., Pantazis, N., Bakoyannis, G., Gioukari, V., Antoniadou, A., Papadopoulos, A., Petrikkos, G., Daikos, G., Psichogiou, M., Gargalianos-Kakolyris, P., Xylomenos, G., Katsarou, O., Kouramba, A., Ioannidou, P., Kordossis, T., Kontos, A., Lazanas, M., Chini, M., Tsogas, N., Panos, G., Paparizos, V., Leuow, K., Kourkounti, S., Sambatakou, H., Mariolis, I., Skoutelis, A., Papastamopoulos, V., Baraboutis, I., Internal medicine, APH - Aging & Later Life, Pediatric surgery, CCA - Innovative therapy, ICaR - Circulation and metabolism, ICaR - Ischemia and repair, Graduate School, Paediatric Infectious Diseases / Rheumatology / Immunology, Landsteiner Laboratory, AII - Amsterdam institute for Infection and Immunity, Infectious diseases, Global Health, Center of Experimental and Molecular Medicine, APH - Amsterdam Public Health, AII - Inflammatory diseases, and ARD - Amsterdam Reproduction and Development
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Adult ,Male ,medicine.medical_specialty ,Adolescent ,Opportunistic infection ,AIDS-Related Opportunistic Infections ,Immunology ,Population ,Retinitis ,HIV Infections ,Article ,17 Psychology And Cognitive Sciences ,Young Adult ,Immune reconstitution inflammatory syndrome ,Antiretroviral Therapy, Highly Active ,Neoplasms ,Virology ,Internal medicine ,medicine ,Humans ,Immunology and Allergy ,education ,Inverse probability weighting ,Aged ,education.field_of_study ,business.industry ,Developed Countries ,Incidence ,Progressive multifocal leukoencephalopathy ,Hazard ratio ,HIV ,virus diseases ,11 Medical And Health Sciences ,Middle Aged ,06 Biological Sciences ,medicine.disease ,United States ,Europe ,Infectious Diseases ,Anti-Retroviral Agents ,Unmasking ,Female ,Cytomegalovirus retinitis ,business - Abstract
Background: There is little information on the incidence of AIDS-defining events which have been reported in the literature to be associated with immune reconstitution inflammatory syndrome (IRIS) after combined antiretroviral therapy (cART) initiation. These events include tuberculosis, mycobacterium avium complex (MAC), cytomegalovirus (CMV) retinitis, progressive multifocal leukoencephalopathy (PML), herpes simplex virus (HSV), Kaposi sarcoma, non-Hodgkin lymphoma (NHL), cryptococcosis and candidiasis.Methods: We identified individuals in the HIV-CAUSAL Collaboration, which includes data from six European countries and the US, who were HIV-positive between 1996 and 2013, antiretroviral therapy naive, aged at least 18 years, hadCD4+ cell count and HIV-RNA measurements and had been AIDS-free for at least 1 month between those measurements and the start of follow-up. For each AIDS-defining event, we estimated the hazard ratio for no cART versus less than 3 and at least 3 months since cART initiation, adjusting for time-varying CD4+ cell count and HIV-RNA via inverse probability weighting.Results: Out of 96 562 eligible individuals (78% men) with median (interquantile range) follow-up of 31 [13,65] months, 55 144 initiated cART. The number of cases varied between 898 for tuberculosis and 113 for PML. Compared with non-cART initiation, the hazard ratio (95% confidence intervals) up to 3 months after cART initiation were 1.21 (0.90-1.63) for tuberculosis, 2.61 (1.05-6.49) for MAC, 1.17 (0.34-4.08) for CMV retinitis, 1.18 (0.62-2.26) for PML, 1.21 (0.83-1.75) for HSV, 1.18 (0.87-1.58) for Kaposi sarcoma, 1.56 (0.82-2.95) for NHL, 1.11 (0.56-2.18) for cryptococcosis and 0.77 (0.40-1.49) for candidiasis.Conclusion: With the potential exception of mycobacterial infections, unmasking IRIS does not appear to be a common complication of cART initiation in high-income countries.
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- 2014
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173. Internal auditing around the World. A Perspective on global regions
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D'Onza, Giuseppe, Allegrini, Marco, Selim, G., Melville, R., and Koutoupis, A.
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- 2014
174. Opportunistic infections and AIDS malignancies early after initiating combination antiretroviral therapy in high-income countries
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Lodi, S. Del Amo, J. Moreno, S. Bucher, H.C. Furrer, H. Logan, R. Sterne, J. Pérez-Hoyos, S. Jarrín, I. Phillips, A. Olson, A. Van Sighem, A. Reiss, P. Sabin, C. Jose, S. Justice, A. Goulet, J. Miró, J.M. Ferrer, E. Meyer, L. Seng, R. Vourli, G. Antoniadou, A. Dabis, F. Vandenhede, M.-A. Costagliola, D. Abgrall, S. Hernán, M.A. Hernan, M. Bansi, L. Hill, T. Sabin, C. Dunn, D. Porter, K. Glabay, A. Orkin, C. Thomas, R. Jones, K. Fisher, M. Perry, N. Pullin, A. Churchill, D. Gazzard, B. Nelson, M. Asboe, D. Bulbeck, S. Mandalia, S. Clarke, J. Delpech, V. Anderson, J. Munshi, S. Post, F. Easterbrook, P. Khan, Y. Patel, P. Karim, F. Duffell, S. Gilson, R. Man, S.-L. Williams, I. Gompels, M. Dooley, D. Schwenk, A. Ainsworth, J. Johnson, M. Youle, M. Lampe, F. Smith, C. Grabowska, H. Chaloner, C. Ismajani Puradiredja, D. Bansi, L. Hill, T. Phillips, A. Sabin, C. Walsh, J. Weber, J. Kemble, C. Mackie, N. Winston, A. Leen, C. Wilson, A. Bezemer, D.O. Gras, L.A.J. Kesselring, A.M. 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Irigoyen, C. Moreno, S. Antela, A. Casado, J.L. Dronda, F. Moreno, A. Pérez, M.J. López, D. Gutiérrez, C. Hernández, B. Pumares, M. Martí, P. García, L. Page, C. García, F. Hernández, J. Peña, A. Muñoz, L. Parra, J. Viciana, P. Leal, M. López-Cortés, L.F. Trastoy, M. Mata, R. Justice, A.C. Fiellin, D.A. Rimland, D. Jones-Taylor, C. Oursler, K.A. Titanji, R. Brown, S. Garrison, S. Rodriguez-Barradas, M. Masozera, N. Goetz, M. Leaf, D. Simberkoff, M. Blumenthal, D. Leung, J. Butt, A. Hoffman, E. Gibert, C. Peck, R. Mattocks, K. Braithwaite, S. Brandt, C. Bryant, K. Cook, R. Conigliaro, J. Crothers, K. Chang, J. Crystal, S. Day, N. Erdos, J. Freiberg, M. Kozal, M. Gandhi, N. Gaziano, M. Gerschenson, M. Good, B. Gordon, A. Goulet, J.L. Kraemer, K. Lim, J. Maisto, S. Miller, P. Mole, L. O'Connor, P. Papas, R. Robins, J.M. Rinaldo, C. Roberts, M. Samet, J. Tierney, B. Whittle, J. Babiker, A. Brettle, R. Darbyshire, J. Gilson, R. Goldberg, D. Hawkins, D. Jaffe, H. Johnson, A. McLean, K. Pillay, D. Cursley, A. Ewings, F. Fairbrother, K. Louisa Gnatiuc, S.L. Murphy, B. Douglas, G. Kennedy, N. Pritchard, J. Andrady, U. Rajda, N. Maw, R. McKernan, S. Drake, S. Gilleran, G. White, D. Ross, J. Toomer, S. Hewart, R. Wilding, H. Woodward, R. Dean, G. Heald, L. Horner, P. Glover, S. Bansaal, D. Eduards, S. Carne, C. Browing, M. Das, R. Stanley, B. Estreich, S. Magdy, A. O'Mahony, C. Fraser, P. Hayman, B. Jebakumar, S.P.R. Joshi, U. Ralph, S. Wade, A. Mette, R. Lalik, J. Summerfield, H. El-Dalil, A. France, J.A. White, C. Robertson, R. Gordon, S. McMillan, S. Morris, S. Lean, C. Vithayathil, K. McLean, L. Winter, A. Gale, D. Jacobs, S. Tayal, S. Short, L. Roberts, M. Green, S. Williams, G. Sivakumar, K. Bhattacharyya, N.D. Monteiro, E. Minton, J. Dhar, J. Nye, F. De Souza, C.B. Isaksen, A. McDonald, L. McLean, K. Franca, A. Hawkins, D. William, L. Jendrulek, I. Peters, B. Shaunak, S. El-Gadi, S. Easterbrook, P.J. Mazhude, C. Gilson, R. Johnstone, R. Fakoya, A. McHale, J. Waters, A. Kegg, S. Mitchell, S. Byrne, P. Johnson, M. Rice, P. Fidler, S. Mullaney, S.A. McCormack, S. David, D. Melville, R. Phillip, K. Balachandran, T. Mabey-Puttock, S. Sukthankar, A. Murphy, C. Wilkins, E. Ahmad, S. Tayal, S. Haynes, J. Evans, E. Ong, E. Das, R. Grey, R. Meaden, J. Bignell, C. Loay, D. Peacock, K. Girgis, M.R. Morgan, B. Palfreeman, A. Wilcox, J. Tobin, J. Tucker, L. Saeed, A.M. Chen, F. Deheragada, A. Williams, O. Lacey, H. Herman, S. Kinghorn, D. Devendra, V.S. Wither, J. Dawson, S. Rowen, D. Harvey, J. Wilkins, E. Bridgwood, A. Singh, G. Chauhan, M. Kellock, D. Young, S. Dannino, S. Kathir, Y. Rooney, G. Currie, J. Fitzgerald, M. Devendra, S. Keane, F. Booth, G. Green, T. Arumainayyagam, J. Chandramani, S. Rajamanoharan, S. Robinson, T. Curless, E. Gokhale, R. Tariq, A. Roberts, M. Williams, O. Luzzi, G. FitzGerald, M. Fairley, I. Wallis, F. Smit, E. Ward, F. Molina, J.M. Loze, B. Morlat, P. Bonarek, M. Bonnet, F. Nouts, C. Louis, I. Raffi, F. Reliquet, V. Sauser, F. Biron, C. Mounoury, O. Hue, H. Brosseau, D. Delfraissy, J.F. Goujard, C. Ghosn, J. Rannou, M.T. Bergmann, J.F. Badsi, E. Rami, A. Diemer, M. Parrinello, M. Girard, P.M. Samanon-Bollens, D. Campa, P. Tourneur, M. Desplanques, N. Livrozet, J.M. Jeanblanc, F. Chiarello, P. Makhloufi, D. Blanc, A.P. Allègre, T. Reynes, J. Baillat, V. Lemoing, V. Merle De Boever, C. Tramoni, C. Cabié, A. Sobesky, G. Abel, S. Beaujolais, V. Pialoux, G. Slama, L. Chakvetadze, C. Berrebi, V. Yeni, P. Bouvet, E. Fournier, I. Gerbe, J. Trepo, C. Koffi, K. Augustin-Normand, C. Miailhes, P. Thoirain, V. Brochier, C. Thomas, R. Souala, F. Ratajczak, M. Beytoux, J. Jacomet, C. Gourdon, F. Rouveix, E. Morelon, S. Dupont, C. Olivier, C. Lortholary, O. Dupont, B. Viard, J.P. Maignan, A. Ragnaud, J.M. Raymond, I. Leport, C. Jadand, C. Jestin, C. Longuet, P. Boucherit, S. Sereni, D. Lascoux, C. Prevoteau, F. Sobel, A. Levy, Y. Lelièvre, J.D. Lascaux, A.S. Dominguez, S. Dumont, C. Aumâitre, H. Delmas, B. Saada, M. Medus, M. Guillevin, L. Salmon, D. Tahi, T. Yazdanpanah, Y. Pavel, S. Marien, M.C. Drenou, B. Beck-Wirth, G. Beck, C. Benomar, M. Katlama, C. Tubiana, R. Ait Mohand, H. Chermak, A. Ben Abdallah, S. Bentata, M. Touam, F. Hoen, B. Drobacheff, C. Folzer, A. Massip, P. Obadia, M. Prudhomme, L. Bonnet, E. Balzarin, F. Pichard, E. Chennebault, J.M. Fialaire, P. Loison, J. Galanaud, P. Boué, F. Bornarel, D. Verdon, R. Bazin, C. Six, M. Ferret, P. Weiss, L. Batisse, D. Gonzales-Canali, G. Tisne-Dessus, D. Devidas, A. Chevojon, P. Turpault, I. Lafeuillade, A. Cheret, A. Philip, G. Morel, P. Timsit, J. Herson, S. Amirat, N. Simon, A. Brancion, C. Cabane, J. Picard, O. Tredup, J. Stein, A. Ravault, I. Chavanet, C. Buisson, M. Treuvetot, S. Choutet, P. Nau, P. Bastides, F. May, T. Boyer, L. Wassoumbou, S. Oksenhendeler, E. Gérard, L. Bernard, L. De Truchis, P. Berthé, H. Domart, Y. Merrien, D. Greder Belan, A. Gayraud, M. Bodard, L. Meudec, A. Beuscart, C. Daniel, C. Pape, E. Vinceneux, P. Simonpoli, A.M. Zeng, A. Fournier, L. Fuzibet, J.G. Sohn, C. Rosenthal, E. Quaranta, M. Dellamonica, P. Chaillou, S. Sabah, M. Audhuy, B. Schieber, A. Moreau, P. Niault, M. Vaillant, O. Huchon, G. Compagnucci, A. De Lacroix Szmania, I. Richier, L. Lamaury, I. Saint-Dizier, F. Garipuy, D. Gastaut, J.A. Drogoul, M.P. Poizot Martin, I. Fabre, G. Lambert De Cursay, G. Abraham, B. Perino, C. Lagarde, P. David, F. Roche-Sicot, J. Saraux, J.L. Leprêtre, A. Fampin, B. Uludag, A. Morin, A.S. Bletry, O. Zucman, D. Regnier, A. Girard, J.J. Quinsat, D.T. Heripret, L. Grihon, F. Houlbert, D. Ruel, M. Chemlal, K. Caron, F. Debab, Y. Tremollieres, F. Perronne, V. Lepeu, G. Slama, B. Perré, P. Miodovski, C. Guermonprez, G. Dulioust, A. Boudon, P. Malbec, D. Patey, O. Semaille, C. Deville, J. Remy, G. Béguinot, I. Galanaud, P. Boue, F. Chambrin, V. Pignon, C. Estocq, G.A. Levy, A. Delfraissy, J.F. Goujard, C. Duracinsky, M. Le Bras, P. Ngussan, M.S. Peretti, D. Medintzeff, N. Lambert, T. Segeral, O. Lezeau, P. Laurian, Y. Weiss, L. Buisson, M. Piketty, C. Karmochkine, M. Batisse, D. Eliaszewitch, M. Jayle, D. Tisne-Dessus, D. Kazatchkine, M. Leport, C. Colasante, U. Jadand, C. Jestin, C. Duval, X. Nouaouia, W. Boucherit, S. Vilde, J.L. Girard, P.M. Bollens, D. Binet, D. Diallo, B. Meyohas, M.C. Fonquernie, L. Lagneau, J.L. Salmon, D. Guillevin, L. Tahi, T. Launay, O. Pietrie, M.P. Sicard, D. Stieltjes, N. Michot, J. Sobel, A. Levy, Y. Bourdillon, F. Lascaux, A.S. Lelievre, J.D. Dumont, C. Dupont, B. Obenga, G. Viard, J.P. Maignan, A. Vittecoq, D. Escaut, L. Bolliot, C. Bricaire, F. Katlama, C. Schneider, L. Herson, S. Simon, A. Iguertsira, M. Stein, A. Tomei, C. Ravaux, I. Dhiver, C. Tissot Dupont, H. Vallon, A. Gallais, J. Gallais, H. Gastaut, J.A. Drogoul, M.P. Fabre, G. Dellamonica, P. Durant, J. Mondain, V. Perbost, I. Cassuto, J.P. Karsenti, J.M. Venti, H. Fuzibet, J.G. Rosenthal, E. Ceppi, C. Quaranta, M. Krivitsky, J.A. Bentata, M. Bouchaud, O. Honore, P. Sereni, D. Lascoux, C. Delgado, J. Rouzioux, C. Burgard, M. Boufassa, L. Peynet, J. Pérez-Hoyos, S. Del Amo, J. Alvarez, D. Monge, S. Muga, R. Sanvisens, A. Clotet, B. Tor, J. Bolao, F. Rivas, I. Vallecillo, G. Del Romero, J. Raposo, P. Rodríguez, C. Vera, M. Hurtado, I. Belda, J. Fernandez, E. Alastrue, I. Santos, C. Tasa, T. Juan, A. Trullen, J. Garcia De Olalla, P. Cayla, J. Masdeu, E. Knobel, H. Mirò, J.M. Sambeat, M.A. Guerrero, R. Rivera, E. Guerrero, R. Marco, A. Quintana, M. Gonzalez, C. Castilla, J. Guevara, M. De Mendoza, C. Zahonero, N. Ortíz, M. Paraskevis, D. Touloumi, G. Pantazis, N. Bakoyannis, G. Gioukari, V. Antoniadou, A. Papadopoulos, A. Petrikkos, G. Daikos, G. Psichogiou, M. Gargalianos-Kakolyris, P. Xylomenos, G. Katsarou, O. Kouramba, A. Ioannidou, P. Kordossis, T. Kontos, A. Lazanas, M. Chini, M. Tsogas, N. Panos, G. Paparizos, V. Leuow, K. Kourkounti, S. Sambatakou, H. Mariolis, I. Skoutelis, A. Papastamopoulos, V. Baraboutis, I. The HIV-CAUSAL Collaboration
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virus diseases - Abstract
Background: There is little information on the incidence of AIDS-defining events which have been reported in the literature to be associated with immune reconstitution inflammatory syndrome (IRIS) after combined antiretroviral therapy (cART) initiation. These events include tuberculosis, mycobacterium avium complex (MAC), cytomegalovirus (CMV) retinitis, progressive multifocal leukoencephalopathy (PML), herpes simplex virus (HSV), Kaposi sarcoma, non-Hodgkin lymphoma (NHL), cryptococcosis and candidiasis. Methods: We identified individuals in the HIV-CAUSAL Collaboration, which includes data from six European countries and the US, who were HIV-positive between 1996 and 2013, antiretroviral therapy naive, aged at least 18 years, hadCD4+ cell count and HIV-RNA measurements and had been AIDS-free for at least 1 month between those measurements and the start of follow-up. For each AIDS-defining event, we estimated the hazard ratio for no cART versus less than 3 and at least 3 months since cART initiation, adjusting for time-varying CD4+ cell count and HIV-RNA via inverse probability weighting. Results: Out of 96 562 eligible individuals (78% men) with median (interquantile range) follow-up of 31 [13,65] months, 55 144 initiated cART. The number of cases varied between 898 for tuberculosis and 113 for PML. Compared with non-cART initiation, the hazard ratio (95% confidence intervals) up to 3 months after cART initiation were 1.21 (0.90-1.63) for tuberculosis, 2.61 (1.05-6.49) for MAC, 1.17 (0.34-4.08) for CMV retinitis, 1.18 (0.62-2.26) for PML, 1.21 (0.83-1.75) for HSV, 1.18 (0.87-1.58) for Kaposi sarcoma, 1.56 (0.82-2.95) for NHL, 1.11 (0.56-2.18) for cryptococcosis and 0.77 (0.40-1.49) for candidiasis. Conclusion: With the potential exception of mycobacterial infections, unmasking IRIS does not appear to be a common complication of cART initiation in high-income countries. © 2014 Wolters Kluwer Health | Lippincott Williams & Wilkins.
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- 2014
175. The Epidemiology of Chronic Venous Diseases
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Michael H. Criqui, Julie O. Denenberg, V. Wooll, Arnost Fronek, A. Adhikari, Melville R. Klauber, and Robert Langer
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medicine.medical_specialty ,education.field_of_study ,business.industry ,Chronic venous insufficiency ,Population ,MEDLINE ,General Medicine ,030204 cardiovascular system & hematology ,medicine.disease ,Thrombosis ,Surgery ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,Epidemiology ,Varicose veins ,medicine ,030212 general & internal medicine ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,education - Abstract
Objective: To review the prevalence of and risk factors for varicose veins, chronic venous insufficiency (CVI) and venous leg ulcers. Data sources: MEDLINE was searched for the terms prevalence and varicose veins, chronic venous insufficiency, or venous leg ulcers. Study selection: The extant world literature (1966–1999) with a minimum of an available English abstract was collected. Ninety-nine studies were reviewed. Data extraction: Data were extracted on prevalence of diseases of the veins in the lower limb, age and gender of the subject populations, and other risk factors for those diseases examined by the original researchers. Data synthesis: The two most prominent risk factors for venous disease are increasing age and female gender. Additional risk factors for venous disease with at least some documentation in the literature include dietary patterns, obesity, physical activity, standing occupations, constrictive clothing, connective tissue laxity, and hormonal differences, including pregnancy. Family history is also a prominent risk factor, suggesting a genetic component. Conclusions: Varicose veins are found more commonly in women, and with increased age. The increase with age is linear, suggesting a constant incidence and cumulative prevalence. CVI is also more common in women and increases with age, but data are limited. Venous leg ulcers are much less common than varicose veins or CVI and show less of a female preponderance, but increase exponentially with age, suggesting a true increasing incidence with age.
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- 2000
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176. Circadian sleep, illumination, and activity patterns in women
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Girardin Jean-Louis, Sonia Ancoli-Israel, Joseph D Assmus, M A Mowen, Robert Langer, Raul S. Sepulveda, Daniel F. Kripke, and Melville R. Klauber
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Senescence ,medicine.medical_specialty ,media_common.quotation_subject ,Activity rhythms ,Experimental and Cognitive Psychology ,Actigraphy ,Time perception ,Audiology ,Developmental psychology ,Behavioral Neuroscience ,medicine ,Wakefulness ,Circadian rhythm ,Psychology ,Daylight saving time ,Vigilance (psychology) ,media_common - Abstract
Patterns of sleep, illumination, and activity of women of different ages were continuously monitored in their natural environments with a wrist activity monitor. Partial correlation analyses were performed to determine relationships between age and sleep and several circadian rhythm measures including the amplitudes, mesors, and timings of sleep, of illumination, and of activity. We found no age-related decline in actigraphic sleep duration. Age was not a significant correlate of circadian rhythm parameters of sleep. Moreover, no age effects were found on daily illumination exposure or on the circadian timing of illumination and activity patterns. However, the level and amplitude of the circadian activity rhythm showed a gradual decline with aging, independent of the time reference (i.e., Daylight Saving Time versus Standard Time) when recordings were obtained. As expected, significant associations were observed between local time reference and the level and timing of peak of illumination patterns. However, changes in local time reference were not significantly and consistently associated with actigraphic sleep or activity measures.
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- 2000
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177. Periodic Leg Movements During Sleep and Sleep Disturbances in Elders
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Raul S. Sepulveda, Shawn D. Youngstedt, William J. Mason, Daniel F. Kripke, and Melville R. Klauber
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Male ,Myoclonus ,Sleep Wake Disorders ,Aging ,medicine.medical_specialty ,Subjective variables ,Nocturnal Myoclonus Syndrome ,Physical medicine and rehabilitation ,Sleep Initiation and Maintenance Disorders ,medicine ,Humans ,Depression (differential diagnoses) ,Aged ,Sleep disorder ,Depression ,business.industry ,Repeated measures design ,Middle Aged ,medicine.disease ,Sleep in non-human animals ,Poor sleep ,Physical therapy ,Female ,Geriatrics and Gerontology ,medicine.symptom ,business - Abstract
BACKGROUND: Periodic limb movements in sleep (PLMS) are an increasingly pervasive disturbance for aging adults. The aims of this experiment were: (a) to describe the index of periodic limb movements in sleep (myoclonus index [MI] in elderly subjects with complaints of poor sleep or depression (N = 22; 68 +/- 5.5 SD years); and (b) to correlate MI with sleep history, depression scores, and objective and subjective indices of sleep. METHOD: Sleep and leg movements were assessed for 5 consecutive nights. Between-subjects, nonparametric correlations were examined between mean MI and sleep history, depression scores, and objective and subjective sleep characteristics. Associations among within-subject night-to-night variabilities of MI, objective, and subjective variables were examined with repeated measures ANCOVA, entering MI as a covariate. RESULTS: A remarkably high level of MI was found (median 25.8 events per hour; 86% of subjects > 5). Nevertheless, no associations were found between MI and sleep disturbance measures. CONCLUSION: These results extend previous reports that PLMS are remarkably persuasive in elderly volunteers and support other reports questioning whether there is a distinct PLMS syndrome.
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- 1998
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178. Hourly profiles of sleep and wakefulness in severely versus mild-moderately demented nursing home patients
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Sonia Ancoli-Israel, Ruth Pat-Horenczyk, Melville R. Klauber, and Tamar Shochat
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Activity Cycles ,Male ,Aging ,Monitoring, Ambulatory ,medicine ,Humans ,Dementia ,Circadian rhythm ,Wakefulness ,Aged ,Morning ,Aged, 80 and over ,business.industry ,Middle Aged ,medicine.disease ,Sleep in non-human animals ,Circadian Rhythm ,Nursing Homes ,Severe dementia ,Anesthesia ,Ambulatory ,Female ,Every Hour ,Geriatrics and Gerontology ,Sleep ,business - Abstract
The purpose of the current study was to examine differences in hour-by-hour sleep/wakefulness profiles between severely and mild-moderately demented patients, and to assess how many elderly patients remain almost fully asleep or nearly fully awake in each hour of a 24-hour period. Sleep/wakefulness patterns of 67 demented nursing home residents (mean age = 85.7 years) were recorded using Actillume recorders. One 24-hour period was used, and numbers of minutes spent asleep or awake were computed for every hour. There were 46 severely demented patients, and 21 mild-moderately demented patients. The amount of sleep and wakefulness recorded for each hour was compared between the two groups. In addition, the frequencies of patients who remained asleep for more than 90% of each hour, and of those who sustained wakefulness for more than 90% of each hour were computed for every hour, and comparisons were again made between the two groups. Multivariate analysis of variance showed a significant effect of dementia group on the percent of sleep/wakefulness over 24 hours (p = 0.028). Subsequent t-tests performed separately for each hour revealed significant differences between the two dementia groups in 13 out of the 24 hours. Significant differences in the frequencies of patients asleep > 90% or awake > 90% of each hour were centered around the early night and early morning hours. Patients with mild-moderate dementia showed a disproportionate amount of wakefulness during the night, whereas, in addition, patients with severe dementia showed a disproportionate amount of sleepiness during the day. With the progression of dementia, both the capacity to maintain sleep and the capacity to maintain wakefulness are impaired, and result in complete fragmentation of sleep/wakefulness during the night and day.
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- 1998
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179. Electron microscope characterization of AgBr heterojunctions with silver carboxylates and their influence on the morphology of developed silver particles in thermally developed photomaterials
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Lilia P. Burleva, Boris B. Bokhonov, Melville R. V. Sahyun, and David R. Whitcomb
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Histology ,Materials science ,Silver halide ,Inorganic chemistry ,Crystal structure ,Epitaxy ,Silver bromide ,Crystal ,Medical Laboratory Technology ,chemistry.chemical_compound ,Crystallography ,chemistry ,Transmission electron microscopy ,Stearate ,Carboxylate ,Anatomy ,Instrumentation - Abstract
Silver halide crystals formed during in situ treatment of silver stearate crystals with various halidizing agents are observed by scanning and transmission electron microscopy to form on the lateral edges of the silver carboxylate crystals. The location of the silver halide phase on the crystal edge is dictated by the anisotropic structure of the silver stearate crystal lattice, specifically, the layered structure in which silver ion layers are separated by long-chain hydrocarbon groups. The formation of AgBr on the lateral faces of these crystals is proposed to be typical not only of the formation of silver halide on silver stearate but also for all silver carboxylates of the general formula [AgCnH2n-1O2]2 when the crystals of these silver carboxylates have anisotropic, layered structures. The silver bromide/silver carboxylate heterojunction in an in situ system has been clearly observed by transmission electron microscopy. The heterojunction is comprised of a distorted silver carboxylate lattice, which accommodates the misalignment between the AgBr and [Ag(O2CR)]2 crystal lattices. The nature of heterojunction between the AgBr and the silver carboxylate when the AgBr is prepared separately from the preparation of the silver carboxylate differs from the in situ heterojunction. In this case, a layered compound, proposed to have a Ag1-xNaxSt composition, forms between the AgBr and the silver stearate which is a unique feature of this interface. The differences in the structure of interfaces formed between the silver halide and the silver fatty acid complex result in different silver particle morphologies during thermal development of exposed photothermographic films. The developed silver is generally filamentary when the photothermographic material contains silver halide prepared by the in situ exchange reaction between silver carboxylate and a brominating agent. If the photothermographic material is prepared from previously synthesized silver halide crystals, the preformed AgBr route, the developed silver generally crystallizes as dendritic crystals. Microsc. Res. Tech. 42:152–172, 1998. © 1998 Wiley-Liss, Inc.
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- 1998
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180. Neurogenic Hypotension in Patients with Severe Head Injuries
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Theresa Gautille, Lawrence F. Marshall, Randall M. Chesnut, Barbara A. Blunt, and Melville R. Klauber
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Adult ,Male ,Adolescent ,Shock, Hemorrhagic ,Diagnosis, Differential ,Central nervous system disease ,Injury Severity Score ,Hypovolemia ,medicine ,Humans ,Registries ,Child ,Aged ,Aged, 80 and over ,Abbreviated Injury Scale ,business.industry ,Infant, Newborn ,Infant ,Furosemide ,Middle Aged ,medicine.disease ,Blood pressure ,Autonomic Nervous System Diseases ,Brain Injuries ,Child, Preschool ,Anesthesia ,Shock (circulatory) ,Etiology ,Female ,Hypotension ,medicine.symptom ,business ,medicine.drug - Abstract
Objective: To examine the occurrence of hypotensive episodes in patients with severe traumatic brain injuries that are not of hypovolemic origin and to investigate possible neurogenic or iatrogenic causes of such episodes. Methods: We reviewed Traumatic Coma Data Bank (TCDB) records of the 248 patients with early hypotension. We attempted to eliminate episodes related to hemorrhagic hypovolemia by excluding patients with (1) extracranial injuries of Abbreviated Injury Scale scores > 3 (n = 99, 40%); (2) postresuscitation hematocrit levels < 35% (n = 76, 30.6%); (3) hematocrit levels decreasing to
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- 1998
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181. A Controlled Trial of Selegiline, Alpha-Tocopherol, or Both as Treatment for Alzheimer's Disease
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Peter B. Woodbury, Eric Pfeiffer, Michael Grundman, Mary Sano, Lon S. Schneider, Melville R. Klauber, Carl W. Cotman, Leon J. Thal, John H. Growdon, Kimberly Schafer, Ronald G. Thomas, and Christopher Ernesto
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medicine.medical_specialty ,Monoamine oxidase inhibitor ,business.industry ,Clinical Dementia Rating ,medicine.drug_class ,Selegiline ,General Medicine ,Placebo ,medicine.disease ,law.invention ,Surgery ,Clinical trial ,Randomized controlled trial ,law ,Internal medicine ,Multicenter trial ,Medicine ,Alzheimer's disease ,business ,medicine.drug - Abstract
Background There is evidence that medications or vitamins that increase the levels of brain catecholamines and protect against oxidative damage may reduce the neuronal damage and slow the progression of Alzheimer's disease. Methods We conducted a double-blind, placebo-controlled, randomized, multicenter trial in patients with Alzheimer's disease of moderate severity. A total of 341 patients received the selective monoamine oxidase inhibitor selegiline (10 mg a day), alpha-tocopherol (vitamin E, 2000 IU a day), both selegiline and alpha-tocopherol, or placebo for two years. The primary outcome was the time to the occurrence of any of the following: death, institutionalization, loss of the ability to perform basic activities of daily living, or severe dementia (defined as a Clinical Dementia Rating of 3). Results Despite random assignment, the base-line score on the Mini–Mental State Examination was higher in the placebo group than in the other three groups, and this variable was highly predictive of the pr...
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- 1997
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182. Prevalence of Sleep-Disordered Breathing in Ages 40–64 Years: A Population-Based Survey
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Melville R. Klauber, D. J. Mullaney, W. J. Mason, Daniel F. Kripke, Deborah L. Wingard, and Sonia Ancoli-Israel
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Adult ,Male ,medicine.medical_specialty ,Population ,Article ,Body Mass Index ,Random Allocation ,Sex Factors ,Sleep Apnea Syndromes ,Physiology (medical) ,Epidemiology ,Ethnicity ,Prevalence ,medicine ,Humans ,Obesity ,Oximetry ,education ,Retrospective Studies ,Sleep disorder ,education.field_of_study ,business.industry ,Incidence ,Age Factors ,Sleep apnea ,Middle Aged ,medicine.disease ,Comorbidity ,Surgery ,Blood pressure ,Female ,Neurology (clinical) ,business ,Body mass index ,Demography - Abstract
Previous research has offered widely varying prevalence estimates for sleep apnea in the population, leaving uncertain which breathing patterns are abnormal. To explore the distribution of sleep apnea in the population and its co-morbidities, random telephone dialing was used between 1990 and 1994 to recruit subjects for a prevalence survey of sleep-disordered breathing in San Diego adults. Events from which blood oxygen desaturationsor = 4% resulted were monitored with home recording instruments, usually for three consecutive nights. Among 190 women ages 40-64 years, a median of 4.3 desaturation events per hour of sleep were observed. A higher median of 6.7 events per hour was observed among 165 men. Frequencies were much higher among members of minority groups, leading to a standard estimate that 16.3% of U.S. Hispanics and racial minorities haveor = 20 events/hour as compared to 4.9% of non-Hispanic Whites ages 40-64. Obesity indicated by body-mass index was the most important demographic predictor of sleep-disordered breathing, followed by age, male gender, and ethnicity. Quality of well-being was not significantly impaired in subjects with more respiratory events; however, there was some increase in blood pressure and wake-within-sleep associated with sleep-disordered breathing. This survey indicates that sleep-disordered breathing is more common, especially among minorities, than had been previously believed, but less co-morbidity may be associated.
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- 1997
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183. Nomina dubia and available names
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Melville, R. V.
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- 1980
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184. The Correlation between Symptoms and Non-Invasive Test Results in Patients Referred for Peripheral Arterial Disease Testing
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Cameron E Bird, Melville R. Klauber, Arnost Fronek, Michael H. Criqui, Robert Langer, and Julie O. Denenberg
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Adult ,Male ,medicine.medical_specialty ,Arteriosclerosis ,Arterial disease ,medicine.medical_treatment ,Blood Pressure ,030204 cardiovascular system & hematology ,Thigh ,03 medical and health sciences ,0302 clinical medicine ,Surveys and Questionnaires ,Angioplasty ,Humans ,Medicine ,030212 general & internal medicine ,Aged ,Pain Measurement ,Aged, 80 and over ,business.industry ,Ultrasonography, Doppler ,Middle Aged ,Intermittent claudication ,Peripheral ,Surgery ,body regions ,medicine.anatomical_structure ,Toe Brachial Index ,Physical therapy ,Female ,medicine.symptom ,Ankle ,Cardiology and Cardiovascular Medicine ,business ,Claudication - Abstract
The WHO/Rose questionnaire has served as the epidemiologic and clinical standard in the assessment of leg pain in patients with peripheral arterial disease (PAD) for over three decades. However, the structure of this questionnaire does not allow assessment of leg-specific (i.e. right versus left) symptoms. We studied 508 patients aged 39–95 years (mean 68 years), initially referred for PAD non-invasive testing. A revised questionnaire, the San Diego Claudication Questionnaire, was administered which allowed determination of leg-specific symptoms and evaluated thigh and buttock as well as calf pain. Leg-specific symptoms were categorized into no pain, pain at rest, non-calf claudication, non-Rose calf claudication, and Rose claudication. At the same visit, the ankle brachial index, the toe brachial index, and peak posterior tibial flow velocity were measured by Doppler ultrasound and five categories of non-invasive results by type and severity of PAD were defined. Legs with previous intervention (Rx), surgery or angioplasty, were evaluated separately. Claudication was reported in 42% of no Rx legs and 50% of Rx legs; 40% of claudication was atypical (not Rose); 64% of no Rx and 81% of Rx legs had PAD by non-invasive testing, and 27% of affected legs had severe PAD. The correlation between the severity of symptoms and the severity of ipsilateral PAD in no Rx legs was r=−0.40, p< 0.001. In Rx legs, this correlation was somewhat less ( r=0.27, p< 0.001) due to more symptomatology at lesser degrees of PAD, suggesting reporting bias and/or more residual disease than evident from non-invasive testing. To our knowledge, these results provide the first comparison between a standardized assessment of leg pain and the severity of ipsilateral PAD by non-invasive testing.
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- 1996
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185. Rationale and Design of a Multicenter Study of Selegiline and α-Tocopherol in the Treatment of Alzheimer Disease Using Novel Clinical Outcomes
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Leon J. Thal, John H. Growdon, Kimberly Schafer, Melville R. Klauber, Ronald G. Thomas, Michael Grundman, Mary Sano, Christopher Ernesto, and Peter B. Woodbury
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Research design ,medicine.medical_specialty ,education.field_of_study ,Clinical Dementia Rating ,business.industry ,Population ,medicine.disease ,Surgery ,law.invention ,Clinical trial ,Psychiatry and Mental health ,Clinical Psychology ,Clinical research ,Randomized controlled trial ,law ,Internal medicine ,medicine ,Dementia ,Geriatrics and Gerontology ,Alzheimer's disease ,education ,business ,Gerontology - Abstract
This report describes the rationale and design of a clinical trial using selegiline (10 mg/day) and alpha-tocopherol (2,000 IU/day) to slow the progression of dementia in Alzheimer disease (AD). This study was developed by the Alzheimer's Disease Cooperative Study (ADCS), a consortium of clinical research centers actively involved in AD research. The major goal of the consortium is to design and conduct clinical investigations leading to the development of treatments for AD. This study uses a randomized double-blind, placebo-controlled, 2 x 2 factorial, parallel group design to test two drugs for the treatment of AD. The primary outcome of the study is the time to reach any one of the following four endpoints: death, institutionalization, loss of two of three basic activities of daily living, and progression of Clinical Dementia Rating (CDR) stage from 2 to 3. Patients with moderately severe disease (CDR = 2) were enrolled and evaluated 10 times over a period of 2 years to determine if these agents reduce the time to reach any endpoint. A database from the Consortium to Establish a Registry for Alzheimer's Disease indicated adequate power analyses to observe a treatment effect on this clinically meaningful outcome measure. Recruitment and baseline characteristics of the population are provided. The rationale for the choice of a factorial design, the use of a novel, clinically meaningful endpoint, and the selection of a cohort of patients with AD of moderate severity are discussed.
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- 1996
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186. Sleep-disordered breathing in African-American elderly
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Melville R. Klauber, Robert Fell, Sonia Ancoli-Israel, Carl Stepnowsky, E Estline, and A Chinn
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Male ,Sleep Wake Disorders ,Pulmonary and Respiratory Medicine ,Pediatrics ,medicine.medical_specialty ,Difficulty Falling Asleep ,Black People ,Critical Care and Intensive Care Medicine ,White People ,Sleep Apnea Syndromes ,Risk Factors ,medicine ,Humans ,Aged ,African american ,Sleep disorder ,business.industry ,Age Factors ,Apnea ,medicine.disease ,Surgery ,Black or African American ,Hypertension ,Sleep disordered breathing ,Breathing ,Female ,medicine.symptom ,business ,Body mass index ,Negroid - Abstract
Although sleep-disordered breathing (SDB) has been shown to be very prevalent in the elderly, little has been done to examine differences between the elderly of different racial groups. It has been well documented that SDB often results in hypertension and that hypertension is more common in African-Americans than in Caucasians. Therefore, one might suspect that SDB might be more common in African-Americans. Caucasians (n = 346) and African-Americans (n = 54) older than 65 yr of age were studied. African-Americans reported less satisfaction with sleep (p = 0.017), more difficulty falling asleep (p0.001), more daytime sleepiness (p = 0.0014), and more frequent morning headaches (p = 0.0043). African-Americans napped 0.8 times more frequently per evening (p = 0.05) and 11 min longer per nap (p = 0.019) than did Caucasians, and they showed a trend toward more total sleep time (428 versus 408 min). Of greater interest was the fact that more African-Americans had severe SDB with a relative risk twofold as great (relative risk = 2.13) as that for Caucasians, which was confirmed in a logistic regression analysis where race was associated with the presence of SDB (RDIor = 30) independently of age, sex, and body mass index. The mean RDI for those African-Americans with severe SDB was significantly higher than that for Caucasians (72.1 versus 43.3; p = 0.014).
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- 1995
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187. Episodic memory changes are associated with the APOE- epsilon 4 allele in nondemented older adults
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Leon J. Thal, Douglas Galasko, David P. Salmon, Mark W. Bondi, Andreas U. Monsch, Nelson Butters, Melville R. Klauber, and Tsunao Saitoh
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Male ,Apolipoprotein E ,Gerontology ,Aging ,medicine.medical_specialty ,Apolipoproteins E ,Cognition ,Alzheimer Disease ,Memory ,Internal medicine ,medicine ,Humans ,Dementia ,Memory disorder ,Risk factor ,Cognitive decline ,Episodic memory ,Alleles ,Aged ,Aged, 80 and over ,Psychological Tests ,California Verbal Learning Test ,Middle Aged ,Verbal Learning ,medicine.disease ,Cross-Sectional Studies ,Female ,Neurology (clinical) ,Psychology - Abstract
Objective: To compare the memory performances of nondemented older adults with and without the epsilon 4 allele of the apolipoprotein E (APOE- epsilon 4). Background: Few studies have examined the cognitive status of subjects at high risk for the development of dementia of the Alzheimer type (DAT). A newly reported risk factor for DAT allows for an examination of the cognitive performances of nondemented subjects who are at risk by virtue of being either heterozygous or homozygous for the APOE- epsilon 4 allele. Methods: The California Verbal Learning Test (CVLT) was administered to 52 nondemented older adults. Subjects were divided into two groups on the basis of the presence (n equals 17) or absence (n equals 35) of one or two APOE- epsilon 4 alleles. Results: APOE- epsilon 4 and non- epsilon 4 groups did not significantly differ in demographic, mental status, and functional characteristics. APOE- epsilon 4 subjects demonstrated significantly poorer mean performances than non- epsilon 4 subjects on nine CVLT variables. Seven group differences remained significant, and three approached significance (0.05 less than p less than 0.10), after the effects of age and gender were taken into account. Six of the 14 APOE- epsilon 4 subjects who completed annual follow-up evaluations developed either DAT or questionable DAT, whereas none of the 26 non- epsilon 4 subjects who received follow-up demonstrated any cognitive decline. Conclusions: Results suggest that episodic memory changes in older adults are associated with APOE- epsilon 4 allele; sensitive cognitive markers such as those of the CVLT may precede the subsequent development of DAT.NEUROLOGY 1995;45: 2203-2206
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- 1995
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188. The role of epidermal growth factor receptor in human gliomas: II. The control of glial process extension and the expression of glial fibrillary acidic protein
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Olivia D. Espiritu, Patricia Y. Kelley, Melville R. Klauber, James D. Hatton, and Hoi Sang U
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Pathology ,medicine.medical_specialty ,Enzyme-Linked Immunosorbent Assay ,Tretinoin ,Biology ,Receptor tyrosine kinase ,Glial scar ,Rats, Sprague-Dawley ,Epidermal growth factor ,Glioma ,Glial Fibrillary Acidic Protein ,Tumor Cells, Cultured ,medicine ,Animals ,Humans ,Epidermal growth factor receptor ,Growth Substances ,Receptor ,Epidermal Growth Factor ,Glial fibrillary acidic protein ,Brain Neoplasms ,medicine.disease ,Immunohistochemistry ,Rats ,ErbB Receptors ,Nerve growth factor ,Bucladesine ,Astrocytes ,biology.protein ,Cancer research ,Glioblastoma ,Neuroglia ,Cell Division - Abstract
✓ Our earlier investigations of the biology of the epidermal growth factor receptor (EGFR) in human gliomas demonstrated that the level of EGFR expression did not directly predict the glioma growth response to EGF, suggesting that the function of the EGFR in glioblastomas might not be limited to mediating the growth effects of EGF. We conducted the current studies to investigate the function(s) of the EGFR not related to growth control in human gliomas. These investigations show that the EGFR mediates the stimulative effects of EGF on glial process extension and glial fibrillary acidic protein (GFAP) expression. In addition, the level of EGFR expression correlates inversely with glioma cell responsiveness to differentiation promoting agents (for example, nerve growth factor and transforming growth factor-β) that act through transmembrane tyrosine kinase receptors. Thus, glioma lines with a high level of EGFR expression (for example, T-98G cells) responded to fewer differentiation promoting factors than lines with a low level of EGFR expression (such as U-373MG cells). Our results suggest that the EGFR in gliomas may participate in mediating the process extension and GFAP stimulative effects of both EGF and other differentiation promoting agents. These properties represent components of the differentiated state in glia because their expression is stimulated by dibutyryl cyclic adenosine monophosphate in normal astrocytes. The involvement of the EGFR in the expression of these glial specific properties suggests that the EGFR may play an important role in glial differentiation.
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- 1995
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189. Sleep in non-institutionalized Alzheimer’s disease patients
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Melville R. Klauber, C. R. Hofstetter, Sonia Ancoli-Israel, J. C. Gillin, and S. S. Campbell
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Male ,Aging ,medicine.medical_specialty ,Cohort Studies ,Sleep debt ,Alzheimer Disease ,Outpatients ,medicine ,Humans ,Dementia ,Longitudinal Studies ,Circadian rhythm ,Social Behavior ,Psychiatry ,Depression (differential diagnoses) ,Aged ,Sleep disorder ,medicine.disease ,Sleep in non-human animals ,Cohort ,Female ,Geriatrics and Gerontology ,Sleep ,Psychology ,Cohort study - Abstract
The sleep of Alzheimer's disease (AD) patients is often disturbed by medications, depression, circadian rhythm changes and sleep disorders. Institutionalization is often precipitated by the effect of the patient's sleep and wakefulness on the caregiver. We examined reports of sleep disturbance in mild AD patients. The study cohort consisted of 246 AD patients and 94 controls. Self-reports of sleep disturbance in mild AD patients were examined as was the relationship of sleep and medication use. Results were compared to those of normal controls, and the patients' responses to the reports of their caregivers. Dementia was assessed with the Mini Mental Status Exam, the Blessed Dementia Scale, the Mattis Dementia Rating Scale, and the Pfeiffer Outpatient Disability Test. The more demented the patients, the more time they spent in bed, the more fragmented their sleep, and the more naps they took. Caregivers reports of increased wandering at night and more aggressive behavior during the day were associated with increased use of sedative-hypnotics and with going to bed early. Lengthy sleep was associated with disruptive behavior. We conclude that increased sleep may be associated with dementia and with more disruptive behavior.
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- 1994
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190. Correspondence.
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Cutler, Lloyd N., Nader, Ralph, Fischer, Richard P., Barlow, Roger, Hornstein, Norman M., and Sahyun, Melville R. V.
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LETTERS to the editor ,CRIMINAL law ,AUTOMOBILE safety ,AUTOMOBILE industry ,ARISTOCRACY (Social class) - Abstract
Presents letters to the editor referencing articles and topics discussed in previous issues. Reaction to Ralph Nader's piece which advocates the enforcement of criminal sanctions against automobile industry executives who violate federal motor vehicle safety standards; Nader's reply to the comment; Lines from articles which echo the phenomenon of American aristocracy of managers and technicians who are backed by machine power in Kurt Vonnegut's book "Player Piano."
- Published
- 1967
191. Comparison of Patients With Central Sleep Apnea
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Robert L. Engler, Daniel F. Kripke, Patrick A. Ross, Paul J. Friedman, Sonia Ancoli-Israel, and Melville R. Klauber
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Pulmonary and Respiratory Medicine ,medicine.medical_specialty ,Sleep disorder ,Central sleep apnea ,business.industry ,Central apnea ,Sleep apnea ,Apnea ,chemical and pharmacologic phenomena ,Critical Care and Intensive Care Medicine ,medicine.disease ,Cheyne–Stokes respiration ,respiratory tract diseases ,Central nervous system disease ,Internal medicine ,Anesthesia ,Heart failure ,Cardiology ,Medicine ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business - Abstract
This study was designed to determine the impact of central sleep apnea with or without Cheyne-Stokes respiration (CSR) on morbidity and mortality. Central sleep apnea was found in 77 male general medical ward in-patients. Cheyne-Stokes respiration was found in 49 of the 77 men; in 15 men, CSR was severe, ie , ≥25 percent of the night spent in CSR, in 34 men CSR was mild (1 to 25 percent CSR). Twenty-eight men had central sleep apnea but no CSR. An additional 31 patients had no sleep apnea and no CSR. The patients with severe CSR had more central apneas, more, but shorter desaturations, more awakenings and more wake time during the night, but spent more time in bed than those with no CSR or no apnea. Radiographic evidence was consistent with an association of CSR and heart failure. In addition, patients with severe CSR were at almost twice the risk of dying compared with those with no apnea and had a shorter survival time. Nevertheless, we could not confirm that CSR was an independent predictor of elevated mortality risk, implying that some other factors specific to severe CSR predispose these patients to shorter survival time.
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- 1994
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192. Early, routine paralysis for intracranial pressure control in severe head injury
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Randall M. Chesnut, John K. Hsiang, Melville R. Klauber, Barbara A. Blunt, Catherine B. Crisp, and Lawrence F. Marshall
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business.industry ,Head injury ,Glasgow Coma Scale ,Retrospective cohort study ,Critical Care and Intensive Care Medicine ,Neuromuscular Blocking Agents ,medicine.disease ,Intensive care unit ,law.invention ,law ,Intensive care ,Anesthesia ,Paralysis ,medicine ,medicine.symptom ,business ,Intracranial pressure - Abstract
ObjectiveTo investigate the efficacy of early, routine use of neuromuscular blocking agents for intracranial pressure management in patients with severe head injury.DesignRetrospective review of data from the Traumatic Coma Data Bank. The Traumatic Coma Data Bank was a collaborative project of the N
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- 1994
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193. Political Talk Radio: A Stereotype Reconsidered
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Carolyn J. Huie, C. Richard Hofstetter, Melville R. Klauber, Mark C. Donovan, Alexandra Cole, and Toshiyuki Yuasa
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education.field_of_study ,Sociology and Political Science ,media_common.quotation_subject ,05 social sciences ,Population ,Political socialization ,Alienation ,Stereotype ,Political communication ,0506 political science ,Politics ,Cynicism ,Political science ,0502 economics and business ,050602 political science & public administration ,Voting behavior ,050207 economics ,education ,Social psychology ,media_common - Abstract
Despite its popularity and controversial character, few studies of political talk radio have been conducted. Little evidence for the hypothesis that political talk radio leads to alienation, social and political isolation, cynicism, and political withdrawal was found among a population-based sample of 525 adults in San Diego, California. Respondents reported widespread exposure to talk radio, although they often did not discriminate accurately among political, nonpolitical, and other program ming. Exposure was associated with traditional forms of political participation, beliefs in self-efficacy linked to specific political behaviors, and psychological involvement in politics. Increased penetration of the public may have altered the nature of the political talk radio audience so that exposure to talk radio is more closely associated with customary forms of political involvement than with social and political alienation.
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- 1994
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194. The Localizing Value of Asymmetry in Pupillary Size in Severe Head Injury
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Melville R. Klauber, Lawrence E. Marshall, Theresa Gautille, Randall Matthew Chesnut, and Barbara A. Blunt
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Anisocoria ,Severe head injury ,business.industry ,media_common.quotation_subject ,medicine.disease ,Asymmetry ,Epidural hematoma ,Anesthesia ,Mechanism of injury ,Medicine ,Surgery ,Neurology (clinical) ,medicine.symptom ,business ,Value (mathematics) ,media_common - Published
- 1994
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195. What’s Next for Internal Auditing?
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Allegrini, Marco, D'Onza, Giuseppe, Melville, R, Sarens, G, and Selim, G.
- Published
- 2011
196. The Biology of Nothofagus
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Melville, R., Godley, E. J., Couper, R. A., James, P. W., and Guiler, E. R.
- Published
- 1960
197. Contributions to the Flora of Australia: IV. Comber's Archeria from Tasmania
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Melville, R.
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- 1957
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198. Contributions to the Flora of Australia: V: The Identity of Calandrinia polyandra Bentham
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Melville, R.
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- 1958
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199. Natural History of Sleep Disordered Breathing in Community Dwelling Elderly
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Allison Kullen, Linda Parker, Robert Fell, Carl Stepnowsky, Melville R. Klauber, Sonia Ancoli-Israel, and Daniel F. Kripke
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Male ,medicine.medical_specialty ,Population ,Body Mass Index ,Oxygen Consumption ,Sleep Apnea Syndromes ,Predictive Value of Tests ,Physiology (medical) ,Respiratory disturbance index ,medicine ,Humans ,Longitudinal Studies ,Oximetry ,Wakefulness ,Intensive care medicine ,education ,Aged ,Sleep disorder ,education.field_of_study ,business.industry ,Snoring ,Apnea ,medicine.disease ,Oxygen ,Predictive value of tests ,Breathing ,Physical therapy ,Female ,Neurology (clinical) ,medicine.symptom ,Respiratory Insufficiency ,business ,Body mass index - Abstract
Mild sleep disordered breathing is very common in the elderly, but little is known about the course of the disorder over time. Twenty-four elderly people from a population-based study were recorded three times over an 8.5-year period. There were no significant changes in either apnea index or in respiratory disturbance index (RDI) over time, even when controlled for body mass index. For most subjects, there was great variability over time in the number of respiratory disturbances. The sensitivity of RDI > or = 15 at visit 1 predicting RDI > or = 15 at visit 3 was only 20%. The predictive value was 50%. Sleep disordered breathing measured at a single point in time is rather weakly predictive of the severity of breathing disorder 4-8 years later.
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- 1993
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200. Blood pressure change and survival after age 75
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Melville R. Klauber, Theodore G. Ganiats, Elizabeth Barrett-Connor, Robert Langer, and Michael H. Criqui
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Male ,Aging ,medicine.medical_specialty ,Blood pressure change ,Systole ,Population ,Diastole ,Blood Pressure ,Prehypertension ,Sex Factors ,Risk Factors ,Internal medicine ,Internal Medicine ,medicine ,Humans ,Mortality ,education ,Antihypertensive Agents ,Aged ,Cardiovascular mortality ,education.field_of_study ,business.industry ,Age Factors ,Survival Analysis ,Confidence interval ,Surgery ,Blood pressure ,Cardiovascular Diseases ,Relative risk ,Cardiology ,Female ,business - Abstract
Higher diastolic pressure predicted better survival in men 75 years or older in two prior analyses in the Rancho Bernardo population. Diastolic change was implicated as a possible explanation. We studied this by assessing survival according to blood pressure change in 795 men and women aged 75 years and older at the time of a second measurement taken an average of 11 years after the first, who were then followed for 5 years. Sex-specific analyses compared participants with a diastolic decrease of 5 mm Hg or greater and participants with a systolic decrease of 10 mm Hg or greater with those whose blood pressure levels did not change or increased. In men, after adjustment for baseline pressure, a decrease in diastolic pressure of 5 mm Hg or greater was associated with higher all-cause mortality (relative risk, 2.33; 95% confidence interval, 1.39 to 3.91) and cardiovascular mortality (3.13, 1.47 to 6.66). The mortality risk was strongest in men who took antihypertensive medication and had a fall in diastolic pressure (12.33, 2.73 to 55.72) compared with treated men whose pressures did not decrease. Among men with isolated systolic hypertension, those treated whose diastolic pressure remained stable had the best survival. A systolic fall in men and a decrease in either diastolic or systolic in women was not associated with poorer survival after adjustment for baseline pressure. We conclude that a fall in diastolic pressure of 5 mm Hg was associated with poor survival in men after age 75. This risk was strongest in men who took antihypertensive medication.
- Published
- 1993
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