Tomé FM - 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: tome fm. 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: tome fm. 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: tome fm. 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. 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

5

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

6

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

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: tome fm. Neuromuscul Disord. 1997 Oct;7 Suppl 1:S70-4. doi: 10.1016/s0960-8966(97)00086-2. Neuromuscul Disord. 1997. PMID: 9392020

8

Nuclear inclusions in oculopharyngeal dystrophy.

Tomé FM, Fardeau M. Tomé FM, et al. Acta Neuropathol. 1980;49(1):85-7. doi: 10.1007/BF00692226. Acta Neuropathol. 1980. PMID: 6243839

9

Expression of dystrophin-associated proteins in dystrophin-positive muscle fibers (revertants) in Duchenne muscular dystrophy.

Matsumura K, Tomé FM, Collin H, Leturcq F, Jeanpierre M, Kaplan JC, Fardeau M, Campbell KP. Matsumura K, et al. Among authors: tome fm. Neuromuscul Disord. 1994 Mar;4(2):115-20. doi: 10.1016/0960-8966(94)90002-7. Neuromuscul Disord. 1994. PMID: 7516752

10

The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13.

Brais B, Xie YG, Sanson M, Morgan K, Weissenbach J, Korczyn AD, Blumen SC, Fardeau M, Tomé FM, Bouchard JP, et al. Brais B, et al. Among authors: tome fm. Hum Mol Genet. 1995 Mar;4(3):429-34. doi: 10.1093/hmg/4.3.429. Hum Mol Genet. 1995. PMID: 7795598

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