Fardeau M - Search Results

1

A homologue of dystrophin is expressed at the neuromuscular junctions of normal individuals and DMD patients, and of normal and mdx mice. Immunological evidence.

Pons F, Augier N, Léger JO, Robert A, Tomé FM, Fardeau M, Voit T, Nicholson LV, Mornet D, Léger JJ. Pons F, et al. Among authors: fardeau m. FEBS Lett. 1991 Apr 22;282(1):161-5. doi: 10.1016/0014-5793(91)80468-i. FEBS Lett. 1991. PMID: 1709117 Free article.

2

Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers.

Marini JF, Pons F, Leger J, Loffreda N, Anoal M, Chevallay M, Fardeau M, Leger JJ. Marini JF, et al. Among authors: fardeau m. Neuromuscul Disord. 1991;1(6):397-409. doi: 10.1016/0960-8966(91)90003-b. Neuromuscul Disord. 1991. PMID: 1822352

3

[Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice].

Fardeau M, Tomé FM, Collin H, Augier N, Pons F, Léger J, Léger J. Fardeau M, et al. C R Acad Sci III. 1990;311(5):197-204. C R Acad Sci III. 1990. PMID: 2119867 French.

4

Ubiquitin and beta-amyloid-protein in inclusion body myositis (IBM), familial IBM-like disorder and oculopharyngeal muscular dystrophy: an immunocytochemical study.

Leclerc A, Tomé FM, Fardeau M. Leclerc A, et al. Among authors: fardeau m. Neuromuscul Disord. 1993 Jul;3(4):283-91. doi: 10.1016/0960-8966(93)90021-b. Neuromuscul Disord. 1993. PMID: 8268725

5

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: fardeau m. Neuromuscul Disord. 1994 Jul;4(4):343-8. doi: 10.1016/0960-8966(94)90070-1. Neuromuscul Disord. 1994. PMID: 7981591

6

Localization of dystrophin and dystrophin-related protein at the electromotor synapse and neuromuscular junction in Torpedo marmorata.

Cartaud A, Ludosky MA, Tomé FM, Collin H, Stetzkowski-Marden F, Khurana TS, Kunkel LM, Fardeau M, Changeux JP, Cartaud J. Cartaud A, et al. Among authors: fardeau m. Neuroscience. 1992 Jun;48(4):995-1003. doi: 10.1016/0306-4522(92)90288-d. Neuroscience. 1992. PMID: 1630633

7

Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD gene.

Pernelle JJ, Chafey P, Chelly J, Wahrmann JP, Kaplan JC, Tomé F, Fardeau M. Pernelle JJ, et al. Among authors: fardeau m. Hum Genet. 1988 Mar;78(3):285. doi: 10.1007/BF00291678. Hum Genet. 1988. PMID: 3346018

8

Storage of phosphorylated desmin in a familial myopathy.

Rappaport L, Contard F, Samuel JL, Delcayre C, Marotte F, Tomè F, Fardeau M. Rappaport L, et al. Among authors: fardeau m. FEBS Lett. 1988 Apr 25;231(2):421-5. doi: 10.1016/0014-5793(88)80863-9. FEBS Lett. 1988. PMID: 3360147 Free article.

9

Immunocytochemical analysis of myosin heavy chains in human fetal skeletal muscles.

Pons F, Léger JO, Chevallay M, Tomé FM, Fardeau M, Léger JJ. Pons F, et al. Among authors: fardeau m. J Neurol Sci. 1986 Dec;76(2-3):151-63. doi: 10.1016/0022-510x(86)90165-6. J Neurol Sci. 1986. PMID: 3540217

10

Deficiency of the 50 kDa dystrophin associated glycoprotein (adhalin) in severe autosomal recessive muscular dystrophies in children native from European countries.

Fardeau M, Matsumura K, Tomé FM, Collin H, Leturcq F, Kaplan JC, Campbell KP. Fardeau M, et al. C R Acad Sci III. 1993 Aug;316(8):799-804. C R Acad Sci III. 1993. PMID: 8044705

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