Search

Your search keyword '"Carboni, N."' showing total 188 results
Start Over Author "Carboni, N."
188 results on '"Carboni, N."'

1. Carotid artery stenting during endovascular thrombectomy for acute ischemic stroke with tandem occlusion: the Italian Registry of Endovascular Treatment in Acute Stroke

Author

Sallustio, Fabrizio, Pracucci, Giovanni, Cappellari, Manuel, Saia, Valentina, Mascolo, Alfredo Paolo, Marrama, Federico, Gandini, Roberto, Koch, Giacomo, Diomedi, Marina, D’Agostino, Federica, Rocco, Alessandro, Da Ros, Valerio, Wlderk, Andrea, Nezzo, Marco, Argirò, Renato, Morosetti, Daniele, Renieri, Leonardo, Nencini, Patrizia, Vallone, Stefano, Zini, Andrea, Bigliardi, Guido, Pitrone, Antonio, Grillo, Francesco, Bracco, Sandra, Tassi, Rossana, Bergui, Mauro, Naldi, Andrea, Carità, Giuseppe, Casetta, Ilaria, Gasparotti, Roberto, Magoni, Mauro, Simonetti, Luigi, Haznedari, Nicolò, Paolucci, Matteo, Mavilio, Nicola, Malfatto, Laura, Menozzi, Roberto, Genovese, Antonio, Cosottini, Mirco, Orlandi, Giovanni, Comai, Alessio, Franchini, Enrica, Pedicelli, Alessandro, Frisullo, Giovanni, Puglielli, Edoardo, Casalena, Alfonsina, Cester, Giacomo, Baracchini, Claudio, Castellano, Davide, Di Liberto, Alessandra, Ricciardi, Giuseppe Kenneth, Chiumarulo, Luigi, Petruzzellis, Marco, Lafe, Elvis, Persico, Alessandra, Cavasin, Nicola, Critelli, Adriana, Semeraro, Vittorio, Tinelli, Angelica, Giorgianni, Andrea, Carimati, Federico, Auteri, William, Rizzuto, Stefano, Biraschi, Francesco, Nicolini, Ettore, Ferrari, Antonio, Melis, Maurizio, Calia, Stefano, Tassinari, Tiziana, Nuzzi, Nunzio Paolo, Corato, Manuel, Sacco, Simona, Squassina, Guido, Invernizzi, Paolo, Gallesio, Ivan, Ruiz, Luigi, Dui, Giovanni, Carboni, Nicola, Amistà, Pietro, Russo, Monia, Maiore, Mario, Zanda, Bastianina, Craparo, Giuseppe, Mannino, Marina, Inzitari, Domenico, Toni, Danilo, Mangiafico, Salvatore, Gasparotti, R., Inzitari, D., Mangiafico, S., Toni, D., Vallone, S., Zini, A., Bergui, M., Causin, F., Ciccone, A., Nencini, P., Saletti, A., Sallustio, F., Tassi, R., Thyrion, F. Zappoli, Pracucci, G., Saia, V., Gandini, R., Da Ros, V., Greco, L., Morosetti, D., Diomedi, M., Nappini, S., Limbucci, N., Renieri, L., Fainardi, E., Verganti, L., Sacchetti, F., Zelent, G., Bigliardi, G., Dell’Acqua, M. L., Picchetto, L., Vandelli, L., Pentore, R., Maffei, S., Nichelli, P., Longo, M., Pitrone, A., Vinci, S. L., Velo, M., Caragliano, A., Tessitore, A., Bonomo, O., Musolino, R., La Spina, P., Casella, C., Fazio, M. C., Grillo, F., Cotroneo, M., Dell’Aera, C., Francalanza, I., Bracco, S., Cioni, S., Gennari, P., Vallone, I. M., Cerase, A., Martini, G., Stura, G., Daniele, D., Cerrato, P., Naldi, A., Onofrio, M., De Vito, A., Azzini, C., Casetta, I., Mardighian, D., Frigerio, M., Magoni, M., Costa, A., Simonetti, L., Cirillo, L., Taglialatela, F., Isceri, S., Princiotta, C., Dall’Olio, M., Cellerini, M., Gentile, M., Piccolo, L., Migliaccio, L., Brancaleoni, L., Naldi, F., Romoli, M., Zaniboni, A., Ruggiero, M., Sanna, A., Haznedari, N., Commodaro, C., Longoni, M., Biguzzi, S., Cordici, F., Malatesta, E., Castellan, L., Mavilio, N., Salsano, G., Malfatto, L., Finocchi, C., Menozzi, R., Piazza, P., Epifani, E., Andreone, A., Scoditti, U., Castellini, P., Latte, L., Grisendi, I., Cosottini, M., Puglioli, M., Lazzarotti, G., Lauretti, D., Mancuso, M., Giannini, N., Maccarone, M., Orlandi, G., Comai, A., Bonatti, G., Nano, G., Ferro, F., Bonatti, M., Dall’Ora, E., Dossi, R. Currò, Turri, E., Turri, M., Colosimo, C., Pedicelli, A., D’Argento, F., Alexandre, A., Frisullo, G., Di Egidio, V., Puglielli, E. G., Ruggero, L., Assetta, M., Casalena, A., Cester, G., Baracchini, C., Viaro, F., Pieroni, A., Vaudano, G., Comelli, C., Di Maggio, L., Castellano, D., Cavallo, R., Duc, E., Chianale, G., Ciceri, E. F. M., Plebani, M., Augelli, R., Zampieri, P., Grazioli, A., Cappellari, M., Forlivesi, S., Tomelleri, G., Micheletti, N., Chiumarulo, L., Zimatore, D. S., Federico, F., Petruzzelli, M., Zappoli, F., Lafe, E., Sanfilippo, G., Sgreccia, A., Martignoni, A., Cavallini, A., Denaro, F., Persico, A., Cagliari, E., Cavasin, N., Quatrale, R., Critelli, A., Burdi, N., Semeraro, V., Lucarelli, N., Ganimede, M. P., Internò, S., Tinelli, A., Prontera, M. P., Pesare, A., Cotroneo, E., Pampana, E., Ricciardi, F., Gigli, R., Pezzella, F. R., Corsi, F., Giorgianni, A., Baruzzi, F., Pellegrino, C., Terrana, A., Versino, M., Delodovici, M. L., Carimati, F., Cariddi, L. Princiotta, Auteri, W., Di Benedetto, O., Silvagni, U., Perrotta, P., Crispino, E., Petrone, A., Stancati, F., Rizzuto, S., Pugliese, P., Pisani, E., Siniscalchi, A., Gaudiano, C., Pirritano, D., Del Giudice, F., Piano, M., Agostoni, E., Motto, C., Gatti, A., Guccione, A., Tortorella, R., Stecco, A., Guzzardi, G., Del Sette, B., Coppo, L., Baldan, J., Romano, D., Siani, A., Locatelli, G., Saponiero, R., Napolitano, R., De Gregorio, M., Volpe, G., Tenuta, M., Guidetti, G., Biraschi, F., Wulbek, A., Falcou, A., Anzini, A., Mancini, A., De Michele, M., Fausti, S., Di Mascio, M. T., Durastanti, L., Sbardella, E., Mellina, V., Nicolini, E., Comelli, S., Ganau, C., Corraine, S., Fusaro, F., Ferrari, A., Schirru, F., Ledda, V., Secci, S., Melis, M., Piras, V., Moller, J., Padolecchia, R., Allegretti, L., Caldiera, V., Calia, S., Ganci, G., Tassinari, T., Sugo, A., De Nicola, M., Giannoni, M., Bruni, S., Gambelli, E., Provinciali, L., Nuzzi, N. P., Marcheselli, S., Corato, M., Scomazzoni, F., Simionato, F., Roveri, L., Filauri, P., Sacco, S., Orlandi, B., De Santis, F., Tiseo, C., Notturno, F., Ornello, R., Pavia, M., Squassina, G., Cobelli, M., Morassi, M., Magni, E., Invernizzi, P., Pepe, F., Bigni, B., Costa, P., Crabbio, M., Griffini, S., Palmerini, F., Piras, M. P., Gallesio, I., Barbero, S., Ferrandi, D., Dui, G., Fancello, M. C., Zedda, S., Ticca, A., Saddi, M. V., Deiana, G., Rossi, R., Carboni, N., Mela, A., Amistà, P., Russo, M., Iannucci, G., Pinna, V., Di Clemente, L., Santi, M., De Boni, A., De Luca, C., Natrella, M., Fanelli, G., Cristoferi, M., Bottacchi, E., Corso, G., Tosi, P., Sessa, M., Giossi, A., Baietti, Null, Romano, G., Meineri, P., Armentano, A., Versace, P., Arcudi, L., Galvano, G., Petralia, B., Feraco, P., Luppi, G., Giometto, B., Bignamini, V., Piffer, S., Meloni, G. B., Fabio, C., Maiore, M., Pintus, F., Pischedda, A., Manca, A., Mongili, C., Zanda, B., Baule, A., Florio, F., Ciccarese, G., Leone, M., Di Viesti, P., Pappalardo, M. P., Craparo, G., Gallo, C., Monaco, S., Mannino, M., Muto, M., Guarnieri, Gl., Andreone, V., Passalacqua, G., Allegritti, M., Caproni, S., Filizzolo, M., Salmaggi, A., Giordano, A., Marini, C., Frattale, I., Lucente, G., Nozzoli, C., and Lupo, F. A.

Subjects
Stent, Acute stroke, Settore MED/37 - Neuroradiologia, Acute stroke Internal carotid artery diseases Stent Thrombectomy, Neurology (clinical), General Medicine, Settore MED/26, Internal carotid artery diseases, Thrombectomy
Abstract

The management of tandem extracranial internal carotid artery and intracranial large vessel occlusion during endovascular thrombectomy (EVT) for acute ischemic stroke (AIS) has been under-investigated. We sought to investigate outcomes of AIS patients with tandem occlusion (TO) treated with carotid artery stenting (CAS) compared to those not treated with CAS (no-CAS) during EVT.We performed a cohort study using data from AIS patients enrolled in the Italian Registry of Endovascular Treatment in Acute Stroke. Outcomes were 3 months' mortality, functional outcome, complete and successful recanalization, any intracranial hemorrhage, parenchymal hematoma and symptomatic intracerebral hemorrhage.Among 466 AIS patients with TO, CAS patients were 122 and no-CAS patients were 226 (118 excluded). After adjustment for unbalanced variables, CAS was associated with a lower rate of 3 months' mortality (OR 0.407, 95% CI 0.171-0.969, p = 0.042). After adjustment for pre-defined variables, CAS was associated with a lower rate of 3 months' mortality (aOR 0.430, 95% CI 0.187-0.989, p = 0.047) and a higher rate of complete recanalization (aOR 1.986, 95% CI 1.121-3.518, p = 0.019), successful recanalization (aOR 2.433, 95% CI 1.263-4.686, p = 0.008) and parenchymal hematoma (aOR 2.876, 95% CI 1.173-7.050, p = 0.021). CAS was associated with lower 3 months mortality (OR 0.373, 95% CI 0.141-0.982, p = 0.046) and higher rates of successful recanalization (OR 2.082, 95% CI 1.099-3.942, p = 0.024) after adjustment for variables associated with 3 months' mortality and successful recanalization, respectively.Among AIS patients with TO, CAS during EVT was associated with a higher rate of successful reperfusion and a lower rate of 3 months' mortality.

Published
2022

10. Muscle magnetic resonance imaging in congenital myasthenic syndromes

Author

Finlayson, S, Morrow, JM, Rodriguez Cruz, PM, Sinclair, CD, Fischmann, A, Thornton, JS, Knight, S, Norbury, R, White, M, Al-Hajjar, M, Carboni, N, Jayawant, S, Robb, SA, Yousry, TA, Beeson, D, and Palace, J

Subjects
Adult, Male, Myasthenic Syndromes, Congenital, Adolescent, diagnosis, muscle, imaging, Middle Aged, Magnetic Resonance Imaging, Young Adult, congenital myasthenia, health services administration, Image Processing, Computer-Assisted, Humans, Female, genetic, Muscle, Skeletal, health care economics and organizations, Research Articles, Research Article, MRI
Abstract

Introduction In this study we investigated muscle magnetic resonance imaging in congenital myasthenic syndromes (CMS). Methods Twenty‐six patients with 9 CMS subtypes and 10 controls were imaged. T1‐weighted (T1w) and short‐tau inversion recovery (STIR) 3‐Tesla MRI images obtained at thigh and calf levels were scored for severity. Results Overall mean the T1w score was increased in GFPT1 and DPAGT1 CMS. T1w scans of the AChR‐deficiency, COLQ, and CHAT subjects were indistinguishable from controls. STIR images from CMS patients did not differ significantly from those of controls. Mean T1w score correlated with age in the CMS cohort. Conclusions MRI appearances ranged from normal to marked abnormality. T1w images seem to be especially abnormal in some CMS caused by mutations of proteins involved in the glycosylation pathway. A non‐selective pattern of fat infiltration or a normal‐appearing scan in the setting of significant clinical weakness should suggest CMS as a potential diagnosis. Muscle MRI could play a role in differentiating CMS subtypes. Muscle Nerve 54: 211–219, 2016

Published
2015

11. LMNA-associated myopathies: The Italian Laminopathies Network experience in a large cohort of patients

Author

Maggi L, D'Amico A, Sivo S, Pane M, Ricci G, Vercelli L, D'Ambrosio P, Scarlato M, Pegoraro E, Toscano A, Benedetti S, Lattanzi G, Bertini E, Mercuri E, Siciliano G, Rodolico C, Mongini T, Previtali S, Carboni N, Bernasconi P, Morandi L., POLITANO, Luisa, Maggi, L, D'Amico, A, Sivo, S, Pane, M, Ricci, G, Vercelli, L, D'Ambrosio, P, Scarlato, M, Pegoraro, E, Toscano, A, Benedetti, S, Lattanzi, G, Bertini, E, Mercuri, E, Siciliano, G, Rodolico, C, Mongini, T, Politano, Luisa, Previtali, S, Carboni, N, Bernasconi, P, and Morandi, L.

Published
2013

13. The empowerment of translational research: lessons from laminopathies

Author

Benedetti, S., Bernasconi, P., Bertini, E., Biagini, E., Boriani, G., Capanni, C., Carboni, N., Cenacchi, G., Columbaro, M., D'Adamo, M., D'Amico, A., D'Apice, M., R, ., Fontana, M., Gambineri, A., Lattanzi, G., Liguori, R., Maraldi, N. M, Mazzanti, L., Mercuri, E., Mongini, T., Morandi, L. O., Neri, I., Nigro, G., Novelli, G., Ortolani, M., Pasquali, R., Pini, A., Petrini, S., Politano, L., Previtali, S., Pucci, L., Rapezzi, C., Ricci, G., Rodolico, Carmelo, Sbraccia, P., Scarano, E., Siciliano, G., Squarzoni, S., Toscano, Antonio, Vercelli, L., Ziacchi, M., Benedetti S, Bernasconi P, Bertini E, Biagini E, Boriani G, Capanni C, Carboni N, Cenacchi G, Columbaro M, D'Adamo M, D'Amico A, D'Apice MR, Fontana M, Gambineri A, Lattanzi G, Liguori R, Maraldi NM, Mazzanti L, Mercuri E, Mongini T, Morandi LO, Neri I, Nigro G, Novelli G, Ortolani M, Pasquali R, Pini A, Petrini S, Politano L, Previtali S, Pucci L, Rapezzi C, Ricci G, Rodolico C, Sbraccia P, Scarano E, Siciliano G, Squarzoni S, Toscano A, Vercelli L, and Ziacchi M

Subjects
Settore MED/09 - Medicina Interna, Lipodystrophy, lcsh:Medicine, Familial Partial Lipodystrophy Type 2, Hutchinson-Gilford Progeria Syndrome, Translational Research, Biomedical, Progeria, Medicine, Genetics(clinical), Pharmacology (medical), Interdisciplinary communication, Muscular Dystrophy, Emery–Dreifuss muscular dystrophy, Muscular dystrophy, Empowerment, Translational Medical Research, Letter to the Editor, Genetics (clinical), interdisciplinary approach to disease, media_common, Medicine(all), integumentary system, Emery-Dreifuss, General Medicine, Laminopathies, Emery-Dreifuss Muscular Dystrophy, Dilated Cardiomyopathy with Conduction Defects, Mandibuloacral Dysplasia, Rare Diseases, Networking activity, interdisciplinary approach to diseases, Lamins, Muscular Dystrophy, Emery-Dreifuss, RARE DISEASES, Laminopathie, Genetic Diseases, Dilated Cardiomyopathy with Conduction Defect, Hutchinson Gilford Progeria Syndrome, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Nuclear Envelope, media_common.quotation_subject, Translational research, NO, Genetic Diseases, Inborn, Humans, Interdisciplinary Communication, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, business.industry, lcsh:R, nutritional and metabolic diseases, medicine.disease, Mandibuloacral dysplasia, Inborn, Settore MED/03 - Genetica Medica, Family medicine, business
Abstract

The need for a collaborative approach to complex inherited diseases collectively referred to as laminopathies, encouraged Italian researchers, geneticists, physicians and patients to join in the Italian Network for Laminopathies, in 2009. Here, we highlight the advantages and added value of such a multidisciplinary effort to understand pathogenesis, clinical aspects and try to find a cure for Emery-Dreifuss muscular dystrophy, Mandibuloacral dysplasia, Hutchinson-Gilford Progeria and forms of lamin-linked cardiomyopathy, neuropathy and lipodystrophy.

Published
2012

14. Partial lipodystrophy associated with muscular dystrophy of unknown genetic origin

Author

Carboni, N, Brancati, F, Cocco, E, Solla, E, D'Apice, M, Mateddu, A, Mcintyre, A, Fadda, E, Mura, M, Lattanzi, G, Piras, R, Maioli, M, Marrosu, G, Novelli, G, Marrosu, M, and Hegele, R

Subjects
Male, Lipodystrophy, Physiology, Siblings, Karyotype, Comorbidity, Middle Aged, Muscular Dystrophies, Body Fat Distribution, Female, Humans, Neurology (clinical), Cellular and Molecular Neuroscience, Physiology (medical), Settore MED/03 - Genetica Medica
Published
2014

16. Quality of justice for a New Social Europe: better access, more equality, better democracy

Author

CARBONI N.

Subjects
Gender Equality - Social Inclusion - Justice - Democracy - Public Value
Abstract

The following article debates a very challenging question about access to justice. This is a very important issue, strictly related to the functioning and working of democracy as a measurement of execution of a Social Europe based on public value. Access to justice has come increasingly to the fore in the last decades, due to the growing of cross-border disputes among European citizens and organizations. The author argues that improving access to justice could help in getting more equality and better democracy across Europe. By a public value approach, the article first analyses the main policies related to access to justice, which have been recently carried out in Europe. Then three main streams are sorted out: the information and communication technology (ICT) as enabler/facilitator, the citizens/ users involvement, the key role of alternative dispute resolution mechanisms and bodies. Finally, the case studies analysis shows that all the above dimensions can contribute to get a fairer and stronger New Social Europe based on an easier, faster and cheaper access to justice especially for people in weak conditions such as the women and the poor. The question of access can be determined by a number of different factors, among them the empowerment of the women/poor in respective societies can play a decisive role. Hence, the more social partners and social services organisations are stronger and rooted in societies, the more individuals can have support, ask for advice and for representation.

Published
2014

20. Congenital myasthenic syndromes due to mutations in ALG2 and ALG14

Author

Cossins, J, Belaya, K, Hicks, D, Salih, M, Finlayson, S, Carboni, N, Liu, W, Maxwell, S, Zoltowska, K, Farsani, G, Laval, S, Seidhamed, M, Donnelly, P, Bentley, D, McGowan, S, Müller, J, Palace, J, Lochmüller, H, and Beeson, D

Subjects
Male, N-linked glycosylation, medicine.medical_specialty, Adolescent, Blotting, Western, DNA Mutational Analysis, Molecular Sequence Data, Neuromuscular transmission, Biology, N-Acetylglucosaminyltransferases, Bioinformatics, Neuromuscular junction, ALG2, Young Adult, 03 medical and health sciences, 0302 clinical medicine, ALG14, Internal medicine, medicine, Humans, Age of Onset, Child, Oligonucleotide Array Sequence Analysis, 030304 developmental biology, Acetylcholine receptor, Myasthenic Syndromes, Congenital, 0303 health sciences, Base Sequence, Muscle weakness, DPAGT1, Original Articles, Congenital myasthenic syndrome, Scientific Commentaries, medicine.disease, Pedigree, RAPSN, medicine.anatomical_structure, Endocrinology, Child, Preschool, congenital myasthenic syndrome, Female, Neurology (clinical), mutation, medicine.symptom, 030217 neurology & neurosurgery
Abstract

Congenital myasthenic syndromes are a heterogeneous group of inherited disorders that arise from impaired signal transmission at the neuromuscular synapse. They are characterized by fatigable muscle weakness. We performed linkage analysis, whole-exome and whole-genome sequencing to determine the underlying defect in patients with an inherited limb-girdle pattern of myasthenic weakness. We identify ALG14 and ALG2 as novel genes in which mutations cause a congenital myasthenic syndrome. Through analogy with yeast, ALG14 is thought to form a multiglycosyltransferase complex with ALG13 and DPAGT1 that catalyses the first two committed steps of asparagine-linked protein glycosylation. We show that ALG14 is concentrated at the muscle motor endplates and small interfering RNA silencing of ALG14 results in reduced cell-surface expression of muscle acetylcholine receptor expressed in human embryonic kidney 293 cells. ALG2 is an alpha-1,3-mannosyltransferase that also catalyses early steps in the asparagine-linked glycosylation pathway. Mutations were identified in two kinships, with mutation ALG2p.Val68Gly found to severely reduce ALG2 expression both in patient muscle, and in cell cultures. Identification of DPAGT1, ALG14 and ALG2 mutations as a cause of congenital myasthenic syndrome underscores the importance of asparagine-linked protein glycosylation for proper functioning of the neuromuscular junction. These syndromes form part of the wider spectrum of congenital disorders of glycosylation caused by impaired asparagine-linked glycosylation. It is likely that further genes encoding components of this pathway will be associated with congenital myasthenic syndromes or impaired neuromuscular transmission as part of a more severe multisystem disorder. Our findings suggest that treatment with cholinesterase inhibitors may improve muscle function in many of the congenital disorders of glycosylation. © 2013 The Author (2013). Published by Oxford University Press on behalf of the Guarantors of Brain.

Published
2013

27. The expression of cyclin-dependent kinase (cdk) inhibitor p27(KIP1) and cyclin E is an independent survival predictor in stage I-II primary gastric B-cell lymphomas (PGL)

Author

Ferreri, Ajm, Ponzoni, M., Giancarlo Pruneri, Rossi, R., Buffa, R., Carboni, N., Baldini, L., Oro, S., Villa, E., Freschi, M., Viale, G., Corradini, P., Ferreri, Ajm, Ponzoni, Maurilio, Pruneri, G, Rossi, R, Buffa, R, Carboni, N, Baldini, L, Dell'Oro, S, Villa, E, Freschi, M, Viale, G, and Corradini, P.

Published
1999

29. LMNA-associated myopathies: The Italian experience in a large cohort of patients

Author

Maggi, L., primary, D'Amico, A., additional, Pini, A., additional, Sivo, S., additional, Pane, M., additional, Ricci, G., additional, Vercelli, L., additional, D'Ambrosio, P., additional, Travaglini, L., additional, Sala, S., additional, Brenna, G., additional, Kapetis, D., additional, Scarlato, M., additional, Pegoraro, E., additional, Ferrari, M., additional, Toscano, A., additional, Benedetti, S., additional, Bernasconi, P., additional, Colleoni, L., additional, Lattanzi, G., additional, Bertini, E., additional, Mercuri, E., additional, Siciliano, G., additional, Rodolico, C., additional, Mongini, T., additional, Politano, L., additional, Previtali, S. C., additional, Carboni, N., additional, Mantegazza, R., additional, and Morandi, L., additional

Published
2014
Full Text
View/download PDF

37. P.5.17 LMNA-associated myopathies: The Italian Laminopathies Network experience in a large cohort of patients

Author

Maggi, L., primary, D’Amico, A., additional, Sivo, S., additional, Pane, M., additional, Ricci, G., additional, Vercelli, L., additional, D’ambrosio, P., additional, Scarlato, M., additional, Pegoraro, E., additional, Toscano, A., additional, Benedetti, S., additional, Lattanzi, G., additional, Bertini, E., additional, Mercuri, E., additional, Siciliano, G., additional, Rodolico, C., additional, Mongini, T., additional, Politano, L., additional, Previtali, S., additional, Carboni, N., additional, Bernasconi, P., additional, and Morandi, L., additional

Published
2013
Full Text
View/download PDF

40. O-4 The Italian Network for Laminopathies

Author

Lattanzi, G., Basso, A., Benedetti, S., Bertini, E., Biagini, E., Boriani, G., Carboni, N., Cenacchi, G., D'Amico, A., D'Apice, M.R., Fontana, M., Gambineri, A., Liguori, R., Mazzanti, L., Mercuri, E., Mongini, T., Morandi, L., Nigro, G., Palladino, A., Pasquali, R., Pini, A., Politano, L., Previtali, S., Rapezzi, C., Ricci, G., and Siciliano, G.

Subjects
Oral Presentations
Published
2011

41. Hypophyseal pathology in AIDS

Author

Mosca, L., Costanzi, G., Antonacci, C., Boldorini, R., Carboni, N., Cristina, S., Liberani, C., parravicini, C., Pirolo, A., and Vago, L.

Subjects
Pituitary gland, AIDS, 6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología [CDU]
Abstract

One hundred and eleven pituitary glands of patients (93 males, 18 females; mean age 32 years, 5 months) who died of fully developed AIDS or ARC were examined under light microscopy with the aid of immunohistochemistry. On post mortem (p.m.) examination a wide series of multiorgan alterations was noticed. Microscopically vanous lesions in both adeno- and neurohypophysis were seen. These ranged from vessel damage to secondaries to systemic infections, neoplasms and functional derangements. Necrotic lumps due to recent infarction could appear in both parts of the gland, while old fibrous scars sustained a previously overcome necrosis. Different pathogens (mainly fungi) could be seen either within the gland or arising from its meningeal surroundings. Examples of tumour pathology were provided by microadenomas, gliosis/gliomas; the frequency of adenomas (11.7%) was similar to that typical of senility. The functional impairment was mainly connected with ACTH cell hyperplasia, which seems in keeping with corticoadrenal or ACTH-receptor damage.

Published
1992

42. C.P.2.05 Molecular analysis of COL6 genes in patients with Bethlem myopathy and Ullrich congenital muscular dystrophy

Author

Martoni, E., primary, Sabatelli, P., additional, Fabris, M., additional, Mercuri, E., additional, Pane, M., additional, Messina, S., additional, Ricci, E., additional, Bertini, E., additional, D’Amico, A., additional, Maioli, M., additional, Marrosu, G., additional, Carboni, N., additional, Calzolari, E., additional, Merlini, L., additional, Gualandi, F., additional, and Ferlini, A., additional

Published
2007
Full Text
View/download PDF

43. Reliability of the Hammersmith functional motor scale for spinal muscular atrophy in a multicentric study

Author

Mercuri, E., primary, Messina, S., additional, Battini, R., additional, Berardinelli, A., additional, Boffi, P., additional, Bono, R., additional, Bruno, C., additional, Carboni, N., additional, Cini, C., additional, Colitto, F., additional, D'Amico, A., additional, Minetti, C., additional, Mirabella, M., additional, Mongini, T., additional, Morandi, L., additional, Dlamini, N., additional, Orcesi, S., additional, Pelliccioni, M., additional, Pane, M., additional, Pini, A., additional, Swan, A.V., additional, Villanova, M., additional, Vita, G., additional, Main, M., additional, Muntoni, F., additional, and Bertini, E, additional

Published
2006
Full Text
View/download PDF

44. Inflammatory pseudotumour of the lung. lmmunohistochemical analysis on four new cases

Author

Barbareschi, M., Ferrero, S., Aldovini, D., Leonardi, E., Colombetti, V., Carboni, N., and Mariscotti, C.

Subjects
Pseudotumour, 6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología [CDU], macromolecular substances, Lung
Abstract

Inflammatory pseudotumour of the lung (I.P.) is a quite rare benign lesion, variously named by different authors. In the present report four new cases of I.P. are presented and immunohistochemically studied with a panel of antibodies. Microscopically, the most prominent histological features were the presence of interlacing bundles of elongated histiocytic-like cells, plasma cell aggregates and lymphoid follicles. Irnmunohistochemistry showed that plasma cells are polyclonal. The spindle cells were negative for desmin, cytokeratins, lysozyme and S-100 and immunoreactive for alpha-l-antichymotrypsin, vimentin and for smoothmuscle alpha-actin. Actin and desmin, were clearly evident in the vessels' smooth muscle layers, highlighting the angioinvasive behaviour of the lesions. Our data are in keeping with literature suggesting that I.P. is due to a mixed histiocytic-myofibroblastic-reactive proliferation and support the inflammatory nature of IP.

Published
1990

46. Angiogenesis in myelodysplastic syndromes

Author

Pruneri, G, primary, Bertolini, F, additional, Soligo, D, additional, Carboni, N, additional, Cortelezzi, A, additional, Ferrucci, P F, additional, Buffa, R, additional, Lambertenghi-Deliliers, G, additional, and Pezzella, F, additional

Published
1999
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results