Eymard B - Search Results

1

Intravenous immunoglobulin for dysphagia of inclusion body myositis.

Cherin P, Pelletier S, Teixeira A, Laforet P, Simon A, Herson S, Eymard B. Cherin P, et al. Among authors: eymard b. Neurology. 2002 Jan 22;58(2):326. doi: 10.1212/wnl.58.2.326. Neurology. 2002. PMID: 11805271 No abstract available.

2

Chronic progressive external ophthalmoplegia with ragged-red fibers: clinical, morphological and genetic investigations in 43 patients.

Laforêt P, Lombès A, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M. Laforêt P, et al. Among authors: eymard b. Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s. Neuromuscul Disord. 1995. PMID: 7496174

3

[Exercise intolerance caused by muscular phosphorylase kinase deficiency. Contribution of in vivo metabolic studies].

Laforêt P, Eymard B, Lombès A, Duboc D, Jehenson P, Rocchiccioli F, Chaussain M, Chateau D, Brunet P, Fardeau M. Laforêt P, et al. Among authors: eymard b. Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Rev Neurol (Paris). 1996. PMID: 8944243 Review. French.

4

Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy.

Laforêt P, de Toma C, Eymard B, Becane HM, Jeanpierre M, Fardeau M, Duboc D. Laforêt P, et al. Among authors: eymard b. Neurology. 1998 Nov;51(5):1454-6. doi: 10.1212/wnl.51.5.1454. Neurology. 1998. PMID: 9818880

5

Relationships among electrophysiological findings and clinical status, heart function, and extent of DNA mutation in myotonic dystrophy.

Lazarus A, Varin J, Ounnoughene Z, Radvanyi H, Junien C, Coste J, Laforet P, Eymard B, Becane HM, Weber S, Duboc D. Lazarus A, et al. Among authors: eymard b. Circulation. 1999 Mar 2;99(8):1041-6. doi: 10.1161/01.cir.99.8.1041. Circulation. 1999. PMID: 10051298

6

[Macrophagic myofasciitis. Study and Research Group on Acquired and Dysimmunity-related muscular diseases (GERMMAD)].

Chérin P, Laforêt P, Ghérardi RK, Authier FJ, Maisonobe T, Coquet M, Mussini JM, Pellissier JF, Eymard B, Herson S. Chérin P, et al. Among authors: eymard b. Presse Med. 2000 Feb 5;29(4):203-8. Presse Med. 2000. PMID: 10705901 Review. French.

7

[Miyoshi distal myopathy: specific signs and incidence].

Eymard B, Laforêt P, Tomé FM, Collin H, Leroy JP, Hauw JJ, Richard I, Beckmann J, Fardeau M. Eymard B, et al. Rev Neurol (Paris). 2000 Feb;156(2):161-8. Rev Neurol (Paris). 2000. PMID: 10743015 French.

8

Gallium-67 scintigraphy in macrophagic myofasciitis.

Chérin P, Authier FJ, Gherardi RK, Romero N, Laforêt P, Eymard B, Herson S, Caillat-Vigneron N. Chérin P, et al. Among authors: eymard b. Arthritis Rheum. 2000 Jul;43(7):1520-6. doi: 10.1002/1529-0131(200007)43:7<1520::AID-ANR16>3.0.CO;2-Q. Arthritis Rheum. 2000. PMID: 10902755 Free article.

9

["MELAS" (A3243G) mutation of mitochondrial DNA: a study of the relationships between the clinical phenotype in 19 patients and morphological and molecular data].

Laforêt P, Ziegler F, Sternberg D, Rouche A, Frachon P, Fardeau M, Eymard B, Lombès A. Laforêt P, et al. Among authors: eymard b. Rev Neurol (Paris). 2000 Dec;156(12):1136-47. Rev Neurol (Paris). 2000. PMID: 11139730 French.

10

[Proximal myotonial myopathy (PROMM): clinical and histology study].

Bassez G, Attarian S, Laforêt P, Azulay JP, Rouche A, Ferrer X, Urtizberea JA, Pellissier JF, Duboc D, Fardeau M, Pouget J, Eymard B. Bassez G, et al. Among authors: eymard b. Rev Neurol (Paris). 2001 Feb;157(2):209-18. Rev Neurol (Paris). 2001. PMID: 11283467 French.

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