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538 results on '"Christmann D"'

1. Rapport 21-13. Formation des chirurgiens/des équipes chirurgicales à la chirurgie robot-assistée. État de la situation actuelle. Propositions d’améliorations

Author

Bagot, M., Pion, M., Vuitton, D.A., Bertrand, D., Bonnin, A., Bontoux, D., Boudjema, K., Bringer, J., Caton, J., Charpentier, B., Chays, A., Christmann, D., Couturier, D., Delpech, M., Deugnier, Y., Dubousset, J., Dussaule, J.C., Fabiani, J.N., Gueant, J.L., Hauet, T., Hubert, J., Huriet, C., Lebranchu, Y., Le Gall, J.Y., Legent, F., Levy-Brul, D., Levy, P., Logeais, Y., Loisance, D., Ludes, B., Malafosse, M., Mandarim-De-Lacerda, C., Mantion, G., Marescaux, J., Michot, F., Mornex, R., Ourabah, R., Poitout, D., Queneau, P., Ricco, J.B., Richard, F., de Saint Julien, J., Sassard, J., Stoltz, J.F., Vouhé, P., Tran Ba Huy, P., Delmas, V., and Vouhe, P.

Published
2022
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3. Malformations cérébrales

Author

Dietemann, J.-L., primary, Koob, M., additional, Audibert, C., additional, Christmann, D., additional, Rotaru, N., additional, and Sebastià Sancho, C., additional

Published
2018
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4. Phacomatoses

Author

Dietemann, J.-L., primary, Koob, M., additional, Rotaru, N., additional, Christmann, D., additional, and Douzal, V., additional

Published
2018
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5. Aortic valve disease augments vesicular microRNA-145-5p to regulate the calcification of valvular interstitial cells via cellular crosstalk

Author

Goody, PR, primary, Christmann, D, additional, Goody, D, additional, Nehl, D, additional, Becker, K, additional, Wilhelm-Jüngling, K, additional, Uchida, S, additional, Moore, JB, additional, Zimmer, S, additional, Bakhtiary, F, additional, Pfeifer, A, additional, Latz, E, additional, Nickenig, G, additional, Jansen, F, additional, and Hosen, MR, additional

Published
2022
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15. The role of noncoding RNAs during aortic valve stenosis

Author

Goody, P.R, primary, Christmann, D, additional, Hosen, M.R, additional, Nehl, D, additional, Goody, D, additional, Niepmann, S.T, additional, Zietzer, A, additional, Duerr, D, additional, Uer, O, additional, Treede, H, additional, Nickenig, G, additional, Pfeifer, A, additional, and Jansen, F, additional

Published
2020
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30. Human anaplasmosis presenting as atypical pneumonitis in France

Author

Remy, V., Hansmann, Y., De Martino S., Christmann, D., and Brouqui, P.

Subjects
Bacterial infections -- Physiological aspects, Pneumonia -- Case studies, Bacterial pneumonia -- Case studies, Statistics, Communicable diseases -- Research, Health, Health care industry
Published
2003

32. [Neurosyphilis: A retrospective study of 13 cases at Strasbourg University Hospital]

Author

Argemi, Xavier, Hansmann, Yves, Martin, Marjolaine, Lefebvre, Nicolas, Douiri, N, Christmann, D, Chanson, Jean-baptiste, Sauer, Arnaud, De Martino, Sylvie, Virulence Bactérienne Précoce : fonctions cellulaires et contrôle de l'infection aigüe et subaigüe, Université de Strasbourg (UNISTRA), Virulence bactérienne précoce : fonctions cellulaires et contrôle de l'infection aiguë et subaiguë, Biopathologie de la Myéline, Neuroprotection et Stratégies Thérapeutiques (BMNST), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM), and Dynamique des interactions hôte pathogène (DIHP)

Subjects
Adult, Male, University, Eye Infections, Bacterial, HIV, VIH, HIV Infections, Middle Aged, Hospitals, [SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology, Neurosyphilis, Diagnosis, Differential, 80 and over, HIV-1, Humans, Female, France, Syphilis, Aged, Retrospective Studies
Abstract

OBJECTIVE: After a decade of constant decline, the number of syphilis cases has been steadily increasing since the 2000s, particularly in HIV infected patients. Neurosyphilis is a rare manifestation of this sexually transmitted disease for which we performed a retrospective study and analyzed clinical manifestations. PATIENTS AND METHODS: We reviewed retrospectively all the neurosyphilis cases admitted to Strasbourg University Hospital between 2004 and 2014. We included and analyzed 13 patients admitted during this period who met the diagnostic criteria for neurosyphilis. RESULTS: Nine of 13 patients had isolated visual manifestations; three (23.1%) experienced posterior uveitis, two (15.4%), panuveitis, and 4 (30.8%) had papillitis. Out of five patients (38.5%) who were HIV positive, three (60%) had a CD4 cell count above 400/mm3 at the time of diagnosis of neurosyphilis. All patients received parenteral penicillin G or cephalosporin, and 5/13 (38.5%) received systemic corticotherapy. CONCLUSION: Ophthalmologists appear as key players in the identification, management and follow-up of neurosyphilis, since ocular findings are key diagnostic features in these patients.

Published
2017
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33. Position de la Société de pathologie infectieuse de langue française à propos de la maladie de Lyme [Lyme disease: The French Infectious Diseases Society's statement]

Author

Hansmann, Y., Chirouze, C., Tattevin, Pierre, Alfandari, S., Caumes, E., Christmann, D., Salomon, J., Michelet, C., Rabaud, C., Roblot, F., Service de maladies infectieuses et tropicales, Hôpital de Hautepierre [Strasbourg], Laboratoire Chrono-environnement - CNRS - UBFC (UMR 6249) (LCE), Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC)-Centre National de la Recherche Scientifique (CNRS), Service des maladies infectieuses et réanimation médicale [Rennes] = Infectious Disease and Intensive Care [Rennes], CHU Pontchaillou [Rennes], Fonction, structure et inactivation d'ARN bactériens, Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service des Maladies Infectieuses et Tropicales [CHRU Nancy], Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Médecine interne [ Poitiers], Centre hospitalier universitaire de Poitiers (CHU Poitiers), Pharmacologie des anti-infectieux (PHAR), Université de Poitiers-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire Chrono-environnement (UMR 6249) (LCE), Centre National de la Recherche Scientifique (CNRS)-Université de Franche-Comté (UFC), Université Bourgogne Franche-Comté [COMUE] (UBFC)-Université Bourgogne Franche-Comté [COMUE] (UBFC), and Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )

Subjects
[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitology
Abstract

National audience; La maladie de Lyme fait l’objet d’une médiatisation importante. De nombreux articles et émissions de radio et de télévision ont contribué à renforcer un sentiment d’état d’alerte concernant cette maladie. L’une des demandes principales des patients est de bénéficier d’une reconnaissance et d’une prise en charge adaptée de leur infection...

Published
2016
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38. Linkage to 18qter differentiates two clinically overlapping syndromes: congenital cataracts-facial dysmorphism-neuropathy (CCFDN) syndrome and Marinesco-Sjogren syndrome

Author

Denys Chaigne, Hélène Dollfus, Jean-Louis Mandel, Flori J, Christmann D, M. Koenig, Ruh D, Gong J, Clotilde Lagier-Tourenne, Michel Mohr, and Flament J

Subjects
Genetics, Pediatrics, medicine.medical_specialty, Ataxia, business.industry, Haplotype, Marinesco–Sjögren syndrome, medicine.disease, Hypotonia, Genetic linkage, Failure to thrive, medicine, Congenital cataracts, medicine.symptom, Psychomotor disorder, business, Letter to JMG, Genetics (clinical)
Abstract

The Marinesco-Sjogren syndrome (MSS) (MIM 248800) is an autosomal recessive condition characterised by cataracts, ataxia, and growth and mental retardation. Chronic myopathy is a common feature. Peripheral neuropathy and acute rhabdomyolysis have been described occasionally in MSS. To date, no gene for it has been localised. Congenital cataracts-facial dysmorphism-neuropathy syndrome (CCFDN) (MIM 604168) is a recently delineated autosomal recessive condition,1 so far only described in a specific gypsy group originating from Bulgaria. This disorder was localised by linkage analysis to 18qter, telomeric to the marker D18S1141.2 CCFDN alleles showed a highly conserved haplotype in the region D18S1141-D18S70-D18S1268 consistent with genetic homogeneity and a single founder mutation. Since then, the disease locus has been reduced to the interval located between markers D18S1095 and D18S1390.3,4 MSS and CCFDN share common clinical features and are considered to be differential diagnoses. Recently, Merlini et al 4 proposed that the CCFDN syndrome and one subtype of MSS (Marinesco-Sjogren/myoglobinuria), also only described in gypsy patients, are genetically identical. We report here the clinical and linkage analysis of one gypsy family and one Turkish family in which patients presented with congenital or juvenile cataracts and ataxia. Both families were initially diagnosed as MSS. However, our study shows that they are clinically and genetically distinct. We found that the gypsy family had CCFDN features and was linked to 18qter whereas the Turkish family had typical MSS features and was not linked to 18qter. Here, we confirm the clinical overlap between the CCFDN and MS syndromes and show that they are distinct genetic entities. ### Family 1 A sister (patient 1) and a brother (patient 2) of Turkish origin were referred to the neuropaediatric clinic because of failure to thrive, psychomotor delay, major ataxia, and hypotonia. They were the fourth and fifth children of healthy, consanguineous parents (fig …

Published
2002
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46. e-Pilly TROP Maladies infectieuses tropicales

Author

Delmont, J., Pichard, Eric, Jauréguiberry, S., Marchou, B., PAROLA, P., Simon, F., Adehossi, E., Fall, Bâ, Baldin, B., Berrebi, A., Berry, A., Beytout, J., Botelho-Nevers, E., Bouchaud, Olivier, Boussinesq, M., Bouvet, E., Brah, S., Brouqui, P., Buffet, P., Chabasse, Dominique, Belval, Challan, Chippaux, J.-P., Christmann, D., Delaporte, E., Dellamonica, P., Develoux, M., Diallo, I., Eholié, S., Ehui, E., Faucher, J.-F., Ficko, C., Garnotel, E., Gautret, P., Girard, P.-M., Hochedez, P., Imbert, P., Jaffré, Y., Kerouédan, D., Lacombe, K., Lagier, J.-C., Lesens, O., Lucht, F., Mahé, A., Malvy, Denis, May, T., Saliou, Mbaye, Michelet, C., Million, M., Minta, D.K., Monsel, G., Morand, J.-J., Patey, O., Perrone, C., Peyramond, D., Piarroux, Renaud, Rabaud, C., Rabier, Valérie, Rammaert, B., Rapp, C., Resnikoff, S., Savini, H., Soula, G., Strobel, M., Sylla, Mamadou, Tattevin, P., Théfenne, H., Tubiana, R, Yazdanpanah, Y., Groupe d'Étude des Interactions Hôte-Pathogène (GEIHP), Université d'Angers (UA), and Laboratoire de Photonique d'Angers (LPHIA)

Subjects
[SDV]Life Sciences [q-bio]
Abstract

L’e-Pilly TROP est un ouvrage d’infectiologie tropicale destiné aux médecins et aux étudiants en médecine des pays francophones du Sud. La prise en compte des différents niveaux de la pyramide sanitaire dans ces pays le rend aussi accessible aux infirmiers des centres de santé communautaires urbains et des structures de santé intermédiaires des zones rurales. Par définition, les Pays En Développement accroissant progressivement leurs capacités de diagnostic biologique et de traitement, les outils de prise en charge correspondent aux moyens des niveaux périphériques comme à ceux des niveaux hospitaliers de référence.

Published
2012

49. Value of (18) F-FDG-PET/CT in patients with favor of unknown origin and unexplained prolonged inflammatory syndrome : a single center analysis experience

Author

Federici, L., Blondet, C., Imperiale, A., Sibilia, J., Pasquali, J.L., Pflumio, F., Goichot, B., Blaison, D., Weber, J.C., Christmann, D., Constantinesco, A., Andrès, E., Service de Biophysique et Médecine Nucléaire, CHU Strasbourg-Université Louis Pasteur - Strasbourg I-Hôpital de Hautepierre [Strasbourg], Service de médecine interne et de nutrition, Hôpital de Hautepierre [Strasbourg], Service de maladies infectieuses et tropicales, neurospin institut d'imagerie biomédicale, and Commissariat à l'énergie atomique et aux énergies alternatives (CEA)

Subjects
[SPI.MECA.BIOM]Engineering Sciences [physics]/Mechanics [physics.med-ph]/Biomechanics [physics.med-ph], [PHYS.MECA.BIOM]Physics [physics]/Mechanics [physics]/Biomechanics [physics.med-ph], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2009
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50. Unusual abdominal localization of cat scratch diseases minicking malignancy on F-18 FDG PET/CT exmination

Author

Imperiale, A., Blondet, C., Ben-Sellem, D., Forestier, E., Mohseni, M., Piemont, Y., Ojeda, M., Christmann, D., Constantinesco, André, Hansmann, Y., Remond, Yves, Service de Biophysique et Médecine Nucléaire, CHU Strasbourg-Université Louis Pasteur - Strasbourg I-Hôpital de Hautepierre [Strasbourg], Service de maladies infectieuses et tropicales, Hôpital de Hautepierre [Strasbourg], Service de maladies infectueuses et tropicales, Laboratoire de bactériologie, Hôpitaux Universitaires de Strasbourg, Service d'hématologie, Centre Hospitalier Emile Muller [Mulhouse] (CH E.Muller Mulhouse), and Groupe Hospitalier de Territoire Haute Alsace (GHTHA)-Groupe Hospitalier de Territoire Haute Alsace (GHTHA)

Subjects
[SPI.MECA.BIOM] Engineering Sciences [physics]/Mechanics [physics.med-ph]/Biomechanics [physics.med-ph], [PHYS.MECA.BIOM] Physics [physics]/Mechanics [physics]/Biomechanics [physics.med-ph], [SPI.MECA.BIOM]Engineering Sciences [physics]/Mechanics [physics.med-ph]/Biomechanics [physics.med-ph], [PHYS.MECA.BIOM]Physics [physics]/Mechanics [physics]/Biomechanics [physics.med-ph], ComputingMilieux_MISCELLANEOUS
Abstract

International audience

Published
2008

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