Fardeau M - Search Results

1

Congenital muscular dystrophy with merosin deficiency.

Tomé FM, Evangelista T, Leclerc A, Sunada Y, Manole E, Estournet B, Barois A, Campbell KP, Fardeau M. Tomé FM, et al. Among authors: fardeau m. C R Acad Sci III. 1994 Apr;317(4):351-7. C R Acad Sci III. 1994. PMID: 8000914

2

[Muscular reconstruction by myogenic cell graft].

Alameddine H, Dehaupas M, Louboutin JP, Hantaï D, Joubert Y, Sébille A, Fardeau M. Alameddine H, et al. Among authors: fardeau m. C R Seances Soc Biol Fil. 1994;188(5-6):553-73. C R Seances Soc Biol Fil. 1994. PMID: 7780797 French.

3

Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q.

Melki J, Abdelhak S, Sheth P, Bachelot MF, Burlet P, Marcadet A, Aicardi J, Barois A, Carriere JP, Fardeau M, et al. Melki J, et al. Among authors: fardeau m. Nature. 1990 Apr 19;344(6268):767-8. doi: 10.1038/344767a0. Nature. 1990. PMID: 1970420

4

[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: fardeau m. Rev Neurol (Paris). 1996 Jun-Jul;152(6-7):458-64. Rev Neurol (Paris). 1996. PMID: 8944243 Review. French.

5

[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. Rev Neurol (Paris). 1996 Jan;152(1):11-9. Rev Neurol (Paris). 1996. PMID: 8729391 French.

6

[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. Among authors: fardeau m. Rev Neurol (Paris). 2000 Feb;156(2):161-8. Rev Neurol (Paris). 2000. PMID: 10743015 French.

7

[The effect of serum from a patient with myeloma and diffuse muscular hypertrophy on the growth of human muscle cells in culture].

Delaporte C, Fardeau M. Delaporte C, et al. Among authors: fardeau m. C R Acad Sci III. 1984;298(3):49-54. C R Acad Sci III. 1984. PMID: 6424890 French.

8

Social identity and the International Classification of Handicaps: an evaluation of the consequences of facioscapulohumeral muscular dystrophy.

Ville I, Ravaud JF, Marchal F, Paicheler H, Fardeau M. Ville I, et al. Among authors: fardeau m. Disabil Rehabil. 1992 Oct-Dec;14(4):168-75. doi: 10.3109/09638289209165856. Disabil Rehabil. 1992. PMID: 1472696

9

Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy.

Billard C, Gillet P, Signoret JL, Uicaut E, Bertrand P, Fardeau M, Barthez-Carpentier MA, Santini JJ. Billard C, et al. Among authors: fardeau m. Neuromuscul Disord. 1992;2(5-6):371-8. doi: 10.1016/s0960-8966(06)80008-8. Neuromuscul Disord. 1992. PMID: 1300185

10

Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands.

Dubowitz V, Fardeau M. Dubowitz V, et al. Among authors: fardeau m. Neuromuscul Disord. 1995 May;5(3):253-8. doi: 10.1016/0960-8966(95)90011-x. Neuromuscul Disord. 1995. PMID: 10712013 No abstract available.

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