Tomé FM - Search Results

1

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: tome fm. Neuromuscul Disord. 1993 Jul;3(4):283-91. doi: 10.1016/0960-8966(93)90021-b. Neuromuscul Disord. 1993. PMID: 8268725

2

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: tome fm. Neuromuscul Disord. 1991;1(2):103-11. doi: 10.1016/0960-8966(91)90057-y. Neuromuscul Disord. 1991. PMID: 1822780

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. Among authors: tome fm. C R Acad Sci III. 1990;311(5):197-204. C R Acad Sci III. 1990. PMID: 2119867 French.

4

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

5

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. C R Acad Sci III. 1994 Apr;317(4):351-7. C R Acad Sci III. 1994. PMID: 8000914

6

Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities.

Fardeau M, Eymard B, Mignard C, Tomé FM, Richard I, Beckmann JS. Fardeau M, et al. Among authors: tome fm. Neuromuscul Disord. 1996 Dec;6(6):447-53. doi: 10.1016/s0960-8966(96)00387-2. Neuromuscul Disord. 1996. PMID: 9027854

7

Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis.

Guicheney P, Vignier N, Helbling-Leclerc A, Nissinen M, Zhang X, Cruaud C, Lambert JC, Richelme C, Topaloglu H, Merlini L, Barois A, Schwartz K, Tomé FM, Tryggvason K, Fardeau M. Guicheney P, et al. Among authors: tome fm. Neuromuscul Disord. 1997 May;7(3):180-6. doi: 10.1016/s0960-8966(97)00460-4. Neuromuscul Disord. 1997. PMID: 9185182

8

Oculopharyngeal muscular dystrophy in France.

Fardeau M, Tomé FM. Fardeau M, et al. Among authors: tome fm. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S30-3. doi: 10.1016/s0960-8966(97)00078-3. Neuromuscul Disord. 1997. PMID: 9392012

9

Genealogical study of oculopharyngeal muscular dystrophy in France.

Brunet G, Tomé FM, Eymard B, Robert JM, Fardeau M. Brunet G, et al. Among authors: tome fm. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S34-7. doi: 10.1016/s0960-8966(97)00079-5. Neuromuscul Disord. 1997. PMID: 9392013

10

Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.

Tomé FM, Chateau D, Helbling-Leclerc A, Fardeau M. Tomé FM, et al. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S63-9. doi: 10.1016/s0960-8966(97)00085-0. Neuromuscul Disord. 1997. PMID: 9392019

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