Lyon-Caen O - Search Results

1

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p.

Hazan J, Fontaine B, Bruyn RP, Lamy C, van Deutekom JC, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y, et al. Hazan J, et al. Hum Mol Genet. 1994 Sep;3(9):1569-73. doi: 10.1093/hmg/3.9.1569. Hum Mol Genet. 1994. PMID: 7833913

2

The phenotype of "pure" autosomal dominant spastic paraplegia.

Dürr A, Brice A, Serdaru M, Rancurel G, Derouesné C, Lyon-Caen O, Agid Y, Fontaine B. Dürr A, et al. Neurology. 1994 Jul;44(7):1274-7. doi: 10.1212/wnl.44.7.1274. Neurology. 1994. PMID: 8035929

3

Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.

Fontaine B, Rime CS, Hazan J, Dürr A, Stevanin G, Penet C, Reboul J, Agid Y, Lyon-Caen O, Baumann N, et al. Fontaine B, et al. Neuromuscul Disord. 1995 Jan;5(1):11-7. doi: 10.1016/0960-8966(94)e0024-3. Neuromuscul Disord. 1995. PMID: 7719135

4

Hereditary thermosensitive neuropathy: an autosomal dominant disorder of the peripheral nervous system.

Magy L, Birouk N, Vallat JM, Gouider R, Maisonobe T, Bouche P, Lyon-Caen O, Fontaine B. Magy L, et al. Neurology. 1997 Jun;48(6):1684-90. doi: 10.1212/wnl.48.6.1684. Neurology. 1997. PMID: 9191787

5

A second-generation genomic screen for multiple sclerosis.

Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, Yaouanq J, Semana G, Cournu-Rebeix I, Lyon-Caen O, Fontaine B; American-French Multiple Sclerosis Genetics Group. Kenealy SJ, et al. Am J Hum Genet. 2004 Dec;75(6):1070-8. doi: 10.1086/426459. Epub 2004 Oct 19. Am J Hum Genet. 2004. PMID: 15494893 Free PMC article.

6

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

Ducros A, Nagy T, Alamowitch S, Nibbio A, Joutel A, Vahedi K, Chabriat H, Iba-Zizen MT, Julien J, Davous P, Goas JY, Lyon-Caen O, Dubois B, Ducrocq X, Salsa F, Ragno M, Burkhard P, Bassetti C, Hutchinson M, Vérin M, Viader F, Chapon F, Levasseur M, Mas JL, Delrieu O, et al. Ducros A, et al. Am J Hum Genet. 1996 Jan;58(1):171-81. Am J Hum Genet. 1996. PMID: 8554054 Free PMC article.

7

[Trigeminal neuralgia. Diagnosis].

Fontaine B, Lyon-Caen O. Fontaine B, et al. Rev Prat. 1995 Apr 15;45(8):999-1000. Rev Prat. 1995. PMID: 7761785 French. No abstract available.

8

[Andermann syndrome in an Algerian family: suggestion of phenotype and genetic homogeneity].

Lesca G, Cournu-Rebeix I, Azoulay-Cayla A, Lyon-Caen O, Barois A, Dulac O, Fontaine B. Lesca G, et al. Rev Neurol (Paris). 2001 Oct;157(10):1279-81. Rev Neurol (Paris). 2001. PMID: 11885521 French.

9

[Spastic paraparesis in adults. Diagnostic orientations].

Gout O, Fontaine B, Lyon-Caen O. Gout O, et al. Rev Neurol (Paris). 1994 Dec;150(12):809-12. Rev Neurol (Paris). 1994. PMID: 7676115 French. No abstract available.

10

Multiple sclerosis and other related inflammatory disorders of the central nervous system: differential diagnosis and treatment.

Lyon-Caen O, Fontaine B, Gout O, Tourbah A. Lyon-Caen O, et al. Acta Neurol Belg. 1994;94(2):92-7. Acta Neurol Belg. 1994. PMID: 8036882 No abstract available.

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