Fardeau M - Search Results

1

Genealogical study of oculopharyngeal muscular dystrophy in France.

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

2

[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study].

Brunet G, Tomé FM, Samson F, Robert JM, Fardeau M. Brunet G, et al. Among authors: fardeau m. Rev Neurol (Paris). 1990;146(6-7):425-9. Rev Neurol (Paris). 1990. PMID: 2204987 Review. French.

3

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

4

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. Neuromuscul Disord. 1996 Dec;6(6):447-53. doi: 10.1016/s0960-8966(96)00387-2. Neuromuscul Disord. 1996. PMID: 9027854

5

Oculopharyngeal muscular dystrophy in France.

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

6

Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.

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

7

Using the full power of linkage analysis in 11 French Canadian families to fine map the oculopharyngeal muscular dystrophy gene.

Brais B, Bouchard JP, Gosselin F, Xie YG, Fardeau M, Tomé FM, Rouleau GA. Brais B, et al. Among authors: fardeau m. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S70-4. doi: 10.1016/s0960-8966(97)00086-2. Neuromuscul Disord. 1997. PMID: 9392020

8

Dysphagia in oculopharyngeal muscular dystrophy: a series of 22 French cases.

Périé S, Eymard B, Laccourreye L, Chaussade S, Fardeau M, Lacau St Guily J. Périé S, et al. Among authors: fardeau m. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S96-9. doi: 10.1016/s0960-8966(97)00091-6. Neuromuscul Disord. 1997. PMID: 9392025

9

Genetic heterogeneity of congenital muscular dystrophy with rigid spine syndrome.

Moghadaszadeh B, Topaloglu H, Merlini L, Muntoni F, Estournet B, Sewry C, Naom I, Barois A, Fardeau M, Tomé FM, Guicheney P. Moghadaszadeh B, et al. Among authors: fardeau m. Neuromuscul Disord. 1999 Oct;9(6-7):376-82. doi: 10.1016/s0960-8966(99)00051-6. Neuromuscul Disord. 1999. PMID: 10545040

10

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

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