Chevallay M - Search Results

1

Dominant and recessive central core disease associated with RYR1 mutations and fetal akinesia.

Romero NB, Monnier N, Viollet L, Cortey A, Chevallay M, Leroy JP, Lunardi J, Fardeau M. Romero NB, et al. Among authors: chevallay m. Brain. 2003 Nov;126(Pt 11):2341-9. doi: 10.1093/brain/awg244. Epub 2003 Aug 22. Brain. 2003. PMID: 12937085

2

Expression of dystrophin-associated glycoproteins during human fetal muscle development: a preliminary immunocytochemical study.

Tomé FM, Matsumura K, Chevallay M, Campbell KP, Fardeau M. Tomé FM, et al. Among authors: chevallay m. Neuromuscul Disord. 1994 Jul;4(4):343-8. doi: 10.1016/0960-8966(94)90070-1. Neuromuscul Disord. 1994. PMID: 7981591

3

[Familial myopathy with desmin storage seen as a granulo-filamentar, electron-dense material with mutation of the alphaB-cristallin gene].

Fardeau M, Vicart P, Caron A, Chateau D, Chevallay M, Collin H, Chapon F, Duboc D, Eymard B, Tomé FM, Dupret JM, Paulin D, Guicheney P. Fardeau M, et al. Among authors: chevallay m. Rev Neurol (Paris). 2000 May;156(5):497-504. Rev Neurol (Paris). 2000. PMID: 10844369 French.

4

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: chevallay m. Neuromuscul Disord. 1995 Sep;5(5):399-413. doi: 10.1016/0960-8966(94)00080-s. Neuromuscul Disord. 1995. PMID: 7496174

5

Distinct contractile protein profile in congenital myotonic dystrophy and X-linked myotubular myopathy.

Soussi-Yanicostas N, Chevallay M, Laurent-Winter C, Tomé FM, Fardeau M, Butler-Browne GS. Soussi-Yanicostas N, et al. Among authors: chevallay m. Neuromuscul Disord. 1991;1(2):103-11. doi: 10.1016/0960-8966(91)90057-y. Neuromuscul Disord. 1991. PMID: 1822780

6

[Congenital muscular dystrophy with merosin deficiency: clinical, histopathological, immunocytochemical and genetic analysis].

Fardeau M, Tomé FM, Helbling-Leclerc A, Evangelista T, Ottolini A, Chevallay M, Barois A, Estournet B, Harpey JP, Fauré S, Guicheney P, Hillaire D. Fardeau M, et al. Among authors: chevallay m. Rev Neurol (Paris). 1996 Jan;152(1):11-9. Rev Neurol (Paris). 1996. PMID: 8729391 French.

7

Late-onset rod myopathy associated with monoclonal gammopathy.

Eymard B, Brouet JC, Collin H, Chevallay M, Bussel A, Fardeau M. Eymard B, et al. Among authors: chevallay m. Neuromuscul Disord. 1993 Sep-Nov;3(5-6):557-60. doi: 10.1016/0960-8966(93)90115-z. Neuromuscul Disord. 1993. PMID: 8186711

8

[Progressive external ophthalmoplegia of mitochondrial origin: contribution of morphological and molecular studies].

Laforêt P, Eymard B, Danan C, Chevallay M, Rouche A, Frachon P, Fardeau M, Lombès A. Laforêt P, et al. Among authors: chevallay m. Rev Neurol (Paris). 1997 Feb;153(1):51-8. Rev Neurol (Paris). 1997. PMID: 9296156 French.

9

Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study.

He Y, Jones KJ, Vignier N, Morgan G, Chevallay M, Barois A, Estournet-Mathiaud B, Hori H, Mizuta T, Tomé FM, North KN, Guicheney P. He Y, et al. Among authors: chevallay m. Neurology. 2001 Oct 9;57(7):1319-22. doi: 10.1212/wnl.57.7.1319. Neurology. 2001. PMID: 11591858

10

[Histopathologic aspects of polymyositis and dermatomyositis. Correlation with the clinical course. Study of 57 cases].

Gayraud M, Tome F, Herson S, Chevallay M, Fardeau M, Godeau P. Gayraud M, et al. Among authors: chevallay m. Ann Med Interne (Paris). 1989;140(6):445-8. Ann Med Interne (Paris). 1989. PMID: 2696397 Review. French.

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