Fontaine B - Search Results

1

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. Among authors: fontaine b. Neurology. 1994 Jul;44(7):1274-7. doi: 10.1212/wnl.44.7.1274. Neurology. 1994. PMID: 8035929

2

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

3

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. Among authors: fontaine b. Neurology. 1997 Jun;48(6):1684-90. doi: 10.1212/wnl.48.6.1684. Neurology. 1997. PMID: 9191787

4

A new locus for autosomal dominant pure spastic paraplegia, on chromosome 2q24-q34.

Fontaine B, Davoine CS, Dürr A, Paternotte C, Feki I, Weissenbach J, Hazan J, Brice A. Fontaine B, et al. Am J Hum Genet. 2000 Feb;66(2):702-7. doi: 10.1086/302776. Am J Hum Genet. 2000. PMID: 10677329 Free PMC article.

5

Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia.

Elleuch N, Depienne C, Benomar A, Hernandez AM, Ferrer X, Fontaine B, Grid D, Tallaksen CM, Zemmouri R, Stevanin G, Durr A, Brice A. Elleuch N, et al. Among authors: fontaine b. Neurology. 2006 Mar 14;66(5):654-9. doi: 10.1212/01.wnl.0000201185.91110.15. Neurology. 2006. PMID: 16534102

6

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. Among authors: fontaine b. Hum Mol Genet. 1994 Sep;3(9):1569-73. doi: 10.1093/hmg/3.9.1569. Hum Mol Genet. 1994. PMID: 7833913

7

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

Dürr A, Davoine CS, Paternotte C, von Fellenberg J, Cogilinicean S, Coutinho P, Lamy C, Bourgeois S, Prud'homme JF, Penet C, Mas JL, Burgunder JM, Hazan J, Weissenbach J, Brice A, Fontaine B. Dürr A, et al. Among authors: fontaine b. Brain. 1996 Oct;119 ( Pt 5):1487-96. doi: 10.1093/brain/119.5.1487. Brain. 1996. PMID: 8931574

8

Systemic autoimmune features and multiple sclerosis: a 5-year follow-up study.

Tourbah A, Clapin A, Gout O, Fontaine B, Liblau R, Batteux F, Stiévenart JL, Weill B, Lubetzki C, Lyon-Caen O. Tourbah A, et al. Among authors: fontaine b. Arch Neurol. 1998 Apr;55(4):517-21. doi: 10.1001/archneur.55.4.517. Arch Neurol. 1998. PMID: 9561980

9

Familial factors influence disability in MS multiplex families. French Multiple Sclerosis Genetics Group.

Brassat D, Azais-Vuillemin C, Yaouanq J, Semana G, Reboul J, Cournu I, Mertens C, Edan G, Lyon-Caen O, Clanet M, Fontaine B. Brassat D, et al. Among authors: fontaine b. Neurology. 1999 May 12;52(8):1632-6. doi: 10.1212/wnl.52.8.1632. Neurology. 1999. PMID: 10331690

10

Localized proton magnetic resonance spectroscopy in relapsing remitting versus secondary progressive multiple sclerosis.

Tourbah A, Stievenart JL, Gout O, Fontaine B, Liblau R, Lubetzki C, Cabanis EA, Lyon-Caen O. Tourbah A, et al. Among authors: fontaine b. Neurology. 1999 Sep 22;53(5):1091-7. doi: 10.1212/wnl.53.5.1091. Neurology. 1999. PMID: 10496272

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