Robert JM - Search Results

1

[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: robert jm. Rev Neurol (Paris). 1990;146(6-7):425-9. Rev Neurol (Paris). 1990. PMID: 2204987 Review. French.

2

Genealogical study of oculopharyngeal muscular dystrophy in France.

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

3

An abnormal concentration of cases of Rendu-Osler disease in the Valserine valley of the French Jura: a genealogical and demographic study.

Bideau A, Brunet G, Heyer E, Plauchu H, Robert JM. Bideau A, et al. Among authors: robert jm. Ann Hum Biol. 1992 May-Jun;19(3):233-47. doi: 10.1080/03014469200002112. Ann Hum Biol. 1992. PMID: 1616282

4

Diffusion of a particular 4.1(-) hereditary elliptocytosis allele in the French Northern Alps.

Brunet G, Ducluzeau MT, Roda L, Lefrancois P, Baklouti F, Delaunay J, Robert JM. Brunet G, et al. Among authors: robert jm. J Biosoc Sci. 1993 Apr;25(2):239-47. doi: 10.1017/s0021932000020526. J Biosoc Sci. 1993. PMID: 8478372

5

Molecular analysis of hereditary elliptocytosis with reduced protein 4.1 in the French Northern Alps.

Feddal S, Brunet G, Roda L, Chabanis S, Alloisio N, Morlé L, Ducluzeau MT, Maréchal J, Robert JM, Benz EJ Jr, et al. Feddal S, et al. Among authors: robert jm. Blood. 1991 Oct 15;78(8):2113-9. Blood. 1991. PMID: 1912588 Free article.

6

[Systematic neonatal detection of Duchenne's muscular dystrophy. Results after 10 years' of experience in Lyons (France)].

Plauchu H, Cordier MP, Carrier HN, Dellamonica C, Dorche C, Guibaud P, Lauras B, Cotte J, Robert JM. Plauchu H, et al. Among authors: robert jm. J Genet Hum. 1987 Aug;35(4):217-30. J Genet Hum. 1987. PMID: 3655748 French.

7

[Neonatal screening for Duchenne muscular dystrophy. The Lyons experience].

Plauchu H, Dellamonica C, Cotte J, Robert JM. Plauchu H, et al. Among authors: robert jm. Rev Med Liege. 1984 May 15;39(10):464-8. Rev Med Liege. 1984. PMID: 6463471 French. No abstract available.

8

Fraser syndrome with renal agenesis in two consanguineous Turkish families.

Francannet C, Lefrançois P, Dechelotte P, Robert E, Malpuech G, Robert JM. Francannet C, et al. Among authors: robert jm, robert e. Am J Med Genet. 1990 Aug;36(4):477-9. doi: 10.1002/ajmg.1320360421. Am J Med Genet. 1990. PMID: 2389805

9

[Registries of malformations in the Rhône-Alps/Auvergne region. Value and limits of monitoring teratogenesis. 11 years' experience (1976-1986)].

Robert E, Francannet C, Robert JM. Robert E, et al. Among authors: robert jm. J Gynecol Obstet Biol Reprod (Paris). 1988;17(5):601-7. J Gynecol Obstet Biol Reprod (Paris). 1988. PMID: 3230269 French.

10

[Atresia of the esophagus. Study of a cluster observed in 1984 in the Rhône-Alpes region].

Danzon A, Robert E, Collet JP, Robert JM. Danzon A, et al. Among authors: robert jm, robert e. Arch Fr Pediatr. 1988 Apr;45(4):231-5. Arch Fr Pediatr. 1988. PMID: 3408305 French.

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