Výsledky vyhledávání - "P M, Gonnaud"

Pramipexole-responsive acute restless arms syndrome after surgery under general anesthesia: Case report and literature review

Autor: P.-M. Gonnaud, M. Saoud, E. Cotte, Clément Dondé, Laure Peter-Derex, F. Pitance

Publikováno v: Revue neurologique. 173(4)

We reported a case of acute restless arms syndrome occurring after colorectal surgery under general anaesthesia. This case was also compared with other cases of restless legs/arms syndromes occurring in a perioperative context through a literature re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::841b99ac2fb841ed8970294260e67fab
https://pubmed.ncbi.nlm.nih.gov/28215429

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L’amyotrophie bulbospinale liée à l’X ou maladie de Kennedy : variations phénotypiques

Autor: Philippe Latour, Philippe Petiot, P.-M. Gonnaud, Emmanuel Broussolle, Christophe Vial, Françoise Bouhour, Nadia Vandenberghe

Publikováno v: Revue Neurologique. 165:31-37

Resume L’amyotrophie bulbospinale liee a l’X, ou maladie de Kennedy, est une maladie neuro-endocrinienne d’evolution lente, liee a une expansion de triplets CAG du gene codant pour le recepteur aux androgenes. La clinique est caracterisee par u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ebbae56c76fd53f79d21b6c02dfe77ca
https://doi.org/10.1016/j.neurol.2008.06.005

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Prise en charge médico-sociale spécifique des épilepsies partielles pharmaco-résistantes

Autor: P.-M. Gonnaud

Publikováno v: Revue Neurologique. 160:301-307

Resume L’emploi figure parmi les premieres preoccupations des personnes epileptiques ; or, celles-ci se heurtent a un taux de chomage particulierement eleve en cas de pharmaco-resistance. Toutefois, la persistance des crises ne resume pas a elle se

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9fde64c8ddb42cbcc1834d22e41f94a5
https://doi.org/10.1016/s0035-3787(04)71211-4

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Contents, Vol. 65, 1994

Autor: R. Tupler, N.G. Laing, H.J. Eyre, M.A. Garrido-Ramos, N.A. Mazurok, S.J. Goss, D. Francis, A. Vandenberghe, S.M. Zakian, L. Kedes, E. Le Guern, M. Gugenheim, C. Bonnebouche, S.A. Lane, P.F.R. Little, M. Cortinovis, C. Meredith, D.A. Miller, E.I. Yantsen, D.F. Callen, E.Kh. Ginsburg, C.H. van Os, G. Melmer, R. Gouider, L. Tiepolo, F. Sturtz, M. Lafage-Pochitaloff, A. Plet, Y. Agid, R. Lozano, B. Chérif-Zahar, Angela Maria Vianna-Morgante, C. Ruiz Rejón, P. Bouche, M Janson, E. Dainotti, I. Siedlaczck, N.M. Matveeva, J.-M. Blanchard, D.O. Weghuis, A. Mincheva, N. Ravisé, J.T. Epplen, David W. Hale, O.J. Miller, T.M. Fink, M. Jamilena, I. Salvignol, A. Brice, A. Geurts van Kessel, P. Maraschio, P.M.T. Deen, B. Wieringa, G. Chazot, S. Tardieu, L.L. Deaven, P. Calvas, I. Todorov, T.B. Nesterova, J. Imbert, C. Cerdan, Q.-Q. Cai, Anne Lise Børresen, Peter Lichter, J.A.M. Graves, P.-M. Gonnaud, D. Depétris, R.A. Sturm, J.L. Cassady, S.D. Wilton, M. Ruiz Rejón, P.A. Akkari, A. Blancher, O. Riess, M.-G. Mattéi, Carla Rosenberg, A.G. Shilov, D.I. Francis, M. Nordeskjöld, D. Werner, S. Kredtke

Publikováno v: Cytogenetic and Genome Research. 65:I-IV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::435361dce90327342265c6b0f6662d9c
https://doi.org/10.1159/000133634

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[Multiple phenotypic manifestations of X-linked spinobulbar muscular atrophy]

Autor: N, Vandenberghe, F, Bouhour, P, Petiot, P-M, Gonnaud, P, Latour, E, Broussolle, C, Vial

Publikováno v: Revue neurologique. 165(1)

Recessive X-linked amyotrophic spinobulbar muscular atrophy (SBMA) or Kennedy disease is a neuroendocrine disorder with a slowly progressive phenotype, caused by an expansion of a polymorphic tandem CAG repeat of the androgen receptor gene. Classical

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b50041d5d531c3dc01a467dd1e5e9dc5
https://pubmed.ncbi.nlm.nih.gov/18667219

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Acute meningoradiculitis concomitant with seroconversion to human immunodeficiency virus type 1

Autor: J.-C. Tardy, H. Poly, R. Tete, K. Kindbeiter, P.-M. Gonnaud, J.-J. Madjar, J. Fontana, P. Paton

Publikováno v: Research in Virology. 141:427-433

We report a case of acute regressive meningoradiculitis concomitant with HIV1 primoinfection. The clinical symptoms were mild and disappeared spontaneously. Electromyographic studies confirmed the regressive demyelinating-type process. The biological

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83d685a52639cbeff598d95cc0eb2222
https://doi.org/10.1016/0923-2516(90)90043-i

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[Diagnostic value of the anti-IgM SGPG Elisa (Bühlmann laboratories AG) in 147 sera with a monoclonal IgM anti-MAG/SGPG antibody-associated neuropathy]

Autor: C, Caudie, F, Bouhour, P, Petiot, P-M, Gonnaud, J-C, Antoine, C, Vial

Publikováno v: Annales de biologie clinique. 65(4)

Binding of monoclonal IgM antibodies in serum to antigens of the peripheral nervous system such as MAG and SG(L)PG was measured by various non standardised methods. In this study we evaluated a new commercially available IgM anti-SGPG ELISA (Bühlman

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::623890f30d68dc1d8eb49820082653bc
https://pubmed.ncbi.nlm.nih.gov/17627917

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[Diagnostic value of autoantibodies to MAG by ELISA Bühlmann in 117 immune-mediated peripheral neuropathies associated with monoclonal IgM to SGPG/SGLPG]

Autor: C, Caudie, F, Kaygisiz, P, Jaquet, P, Petiot, P-M, Gonnaud, J-C, Antoine, C, Vial

Publikováno v: Annales de biologie clinique. 64(4)

The neuropathies associated with monoclonal IgM gammopathy reacted with glycoconjugated targets on a very antigenic epitope on the sulfated glucuronic glycolipids corresponding to SGPG and SGLPG (sulfoglucuronyl paragloboside and sulfoglucuronyl lact

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5985185af682ce2d408ee72b5f67d7cf
https://pubmed.ncbi.nlm.nih.gov/16829480

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Diffusion-weighted magnetic resonance imaging in Marchiafava-Bignami disease: follow-up studies

Autor: Chadi Hlaihel, V. A. Tran-Minh, François Cotton, P.-M. Gonnaud, H. Rousset, S. Champin

Publikováno v: Neuroradiology. 47(7)

Marchiafava-Bignami disease (MBD), an acute toxic demyelination of the corpus callosum in alcoholics, is associated with poor evolution in the majority of patients. We report here the early and late diffusion magnetic resonance imaging (MRI) and appa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43525af83da2c9336fb76a4b2d614b2f
https://pubmed.ncbi.nlm.nih.gov/15918025

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