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You search for a phrase ""Eymard, B."" according to the criterion: Author


Title:
Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins)
Authors:
Mosbah, H.Aff1, Aff2
Donadille, B.
Vatier, C.Aff1, Aff2
Janmaat, S.Aff1, Aff2
Atlan, M.Aff2, Aff3
Badens, C.
Barat, P.
Béliard, S.
Beltrand, J.
Ben Yaou, R.
Bismuth, E.
Boccara, F.
Cariou, B.
Chaouat, M.
Charriot, G.
Christin-Maitre, S.Aff1, Aff2, Aff14
De Kerdanet, M.
Delemer, B.
Disse, E.
Dubois, N.
Eymard, B.
Fève, B.Aff1, Aff2
Lascols, O.Aff2, Aff18
Mathurin, P.
Nobécourt, E.
Poujol-Robert, A.
Prevost, G.
Richard, P.
Sellam, J.Aff2, Aff24
Tauveron, I.
Treboz, D.
Vergès, B.
Vermot-Desroches, V.
Wahbi, K.
Jéru, I.Aff2, Aff18
Vantyghem, M. C.
Vigouroux, C.Aff1, Aff2, Aff18, IDs13023022023087_cor37
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Source:
Orphanet Journal of Rare Diseases. 17(Suppl 1)
Academic Journal
Title:
Myofibrillar myopathies: State of the art, present and future challenges
Authors:
Béhin, A.
Salort-Campana, E.
Wahbi, K.
Richard, P.
Carlier, R.-Y.
Carlier, P.
Laforêt, P.
Stojkovic, T.
Maisonobe, T.
Verschueren, A.
Franques, J.
Attarian, S.
Maues de Paula, A.
Figarella-Branger, D.
Bécane, H.-M.
Nelson, I.
Duboc, D.
Bonne, G.
Vicart, P.
Udd, B.
Romero, N.
Pouget, J.
Eymard, B.
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Alternate Title:
Myopathies myofibrillaires : connaissances acquises, défis présents et futurs (French)
Source:
In Revue Neurologique October 2015 171(10):715-729
Academic Journal
Title:
Forme infantile de la dystrophie myotonique de type 1 (DM1) et troubles du spectre autistique (TSA) : existe-t-il une comorbidité ?
Authors:
Huerta, E.
Jacquette, A.
Cohen, D.
Gargiulo, M.
Servais, L.
Eymard, B.
Héron, D.
Angeard, N.
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Alternate Title:
Childhood form of myotonic dystrophy type 1 and autism spectrum disorders: Is there a comorbidity? (English)
Source:
In Neuropsychiatrie de l'enfance et de l'adolescence March 2015 63(2):91-98
Academic Journal
Title:
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe disease
Authors:
Laforêt, P.
Laloui, K.
Granger, B.
Hamroun, D.
Taouagh, N.
Hogrel, J.-Y.
Orlikowski, D.
Bouhour, F.
Lacour, A.
Salort-Campana, E.
Penisson-Besnier, I.
Sacconi, S.
Zagnoli, F.
Chapon, F.
Eymard, B.
Desnuelle, C.
Pouget, J.
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Alternate Title:
Registre Français de la maladie de Pompe. Caractérisation d’une cohorte de 126 patients adultes (French)
Source:
In Revue Neurologique August-September 2013 169(8-9):595-602
Academic Journal
Title:
Attitudes and expectations of patients with neuromuscular diseases about their participation in a clinical trial
Authors:
Gargiulo, M.
Herson, A.
Michon, C.C.
Hogrel, J.Y.
Doppler, V.
Laloui, K.
Herson, S.
Payan, C.
Eymard, B.
Laforêt, P.
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Alternate Title:
Attitudes et attentes des patients atteints de maladies neuromusculaires, inclus dans un essai clinique (French)
Source:
In Revue Neurologique August-September 2013 169(8-9):670-676
Academic Journal
Title:
Syndromes myasthéniques congénitaux : difficultés diagnostiques, évolution et pronostic, thérapeutique L’expérience du réseau national « Syndromes Myasthéniques Congénitaux »
Authors:
Eymard, B.
Stojkovic, T.
Sternberg, D.
Richard, P.
Nicole, S.
Fournier, E.
Béhin, A.
Laforêt, P.
Servais, L.
Romero, N.
Fardeau, M.
Hantaï, D.
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Alternate Title:
Congenital myasthenic syndromes: difficulties in the diagnosis, course and prognosis, and therapy - The French national Congenital Myasthenic Syndrome network experience (English)
Source:
In Revue Neurologique February 2013 169 Supplement 1:S45-S55
Academic Journal
Title:
Diagnostic strategy for limb-girdle muscular dystrophies
Authors:
Eymard, B.
Lévy, N.
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Alternate Title:
Stratégie diagnostique des dystrophies des ceintures (French)
Source:
In Revue Neurologique December 2012 168(12):919-926
Academic Journal
Title:
Quel potentiel de développement et quels consommateurs à l'international pour les vins rosés ?
Authors:
Eymard B.
Amato Brice
Delerins R.C.
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Subject Terms:
Microbiology
QR1-502
Physiology
QP1-981
Zoology
QL1-991
Source:
BIO Web of Conferences, Vol 15, p 03008 (2019)
File Description:
electronic resource
Relation:
https://www.bio-conferences.org/articles/bioconf/full_html/2019/04/bioconf-oiv2019_03008/bioconf-oiv2019_03008.html; https://doaj.org/toc/2117-4458
Access URL:
https://doaj.org/article/547bca6c573e469abf04776a1421039e  Link opens in a new window
Academic Journal
Title:
The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literature
Authors:
Jallouli, M.
Saadoun, D.
Eymard, B.
Leroux, G.
Haroche, J.
Le Thi Huong, D.
De Gennes, C.
Chapelon, C.
Benveniste, O.
Wechsler, B.
Cacoub, P.
Amoura, Z.
Piette, J. C.
Costedoat-Chalumeau, N.
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Source:
Journal of Neurology: Official Journal of the European Neurological Society. July 2012 259(7):1290-1297
Academic Journal
Title:
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7
Authors:
Ben Ammar, A.
Petit, F.
Alexandri, N.
Gaudon, K.
Bauché, S.
Rouche, A.
Gras, D.
Fournier, E.
Koenig, J.
Stojkovic, T.
Lacour, A.
Petiot, P.
Zagnoli, F.
Viollet, L.
Pellegrini, N.
Orlikowski, D.
Lazaro, L.
Ferrer, X.
Stoltenburg, G.
Paturneau-Jouas, M.
Hentati, F.
Fardeau, M.
Sternberg, D.
Hantaï, D.
Richard, P.
Eymard, B.
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Source:
Journal of Neurology: Official Journal of the European Neurological Society. May 2010 257(5):754-766
Academic Journal

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