Fardeau M - Search Results

1

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

2

[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.

3

Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle.

Khurana TS, Watkins SC, Chafey P, Chelly J, Tomé FM, Fardeau M, Kaplan JC, Kunkel LM. Khurana TS, et al. Among authors: fardeau m. Neuromuscul Disord. 1991;1(3):185-94. doi: 10.1016/0960-8966(91)90023-l. Neuromuscul Disord. 1991. PMID: 1822793

4

Expression of a recombinant dystrophin in mdx mice using adenovirus vector.

Alameddine HS, Quantin B, Cartaud A, Dehaupas M, Mandel JL, Fardeau M. Alameddine HS, et al. Among authors: fardeau m. Neuromuscul Disord. 1994 May;4(3):193-203. doi: 10.1016/0960-8966(94)90020-5. Neuromuscul Disord. 1994. PMID: 7919968

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

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

7

Ultrastructure of muscle and neuromuscular junction: an historical survey of the early French contributions.

Fardeau M, Tomé FM. Fardeau M, et al. Biol Cell. 1994;80(2-3):115-7. doi: 10.1111/j.1768-322x.1994.tb00918.x. Biol Cell. 1994. PMID: 8087060 Review. No abstract available.

8

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

9

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.

10

Etiology and pathogenesis of the muscular dystrophies.

Van den Bergh PY, Tomé FM, Fardeau M. Van den Bergh PY, et al. Among authors: fardeau m. Acta Neurol Belg. 1995;95(3):123-41. Acta Neurol Belg. 1995. PMID: 7484050 Review.

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