Lyon-Caen O - Search Results

1

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.

2

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

3

The natural course of cerebral lesions in Sneddon syndrome.

Tourbah A, Piette JC, Iba-Zizen MT, Lyon-Caen O, Godeau P, Francès C. Tourbah A, et al. Arch Neurol. 1997 Jan;54(1):53-60. doi: 10.1001/archneur.1997.00550130037013. Arch Neurol. 1997. PMID: 9006414

4

Encephalitis after hepatitis B vaccination: recurrent disseminated encephalitis or MS?

Tourbah A, Gout O, Liblau R, Lyon-Caen O, Bougniot C, Iba-Zizen MT, Cabanis EA. Tourbah A, et al. Neurology. 1999 Jul 22;53(2):396-401. doi: 10.1212/wnl.53.2.396. Neurology. 1999. PMID: 10430433

5

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

6

In vivo localized NMR proton spectroscopy of normal appearing white matter in patients with multiple sclerosis.

Tourbah A, Stievenart JL, Iba-Zizen MT, Zannoli G, Lyon-Caen O, Cabanis EA. Tourbah A, et al. J Neuroradiol. 1996 Sep;23(2):49-55. J Neuroradiol. 1996. PMID: 8948157

7

Magnetic resonance imaging using FLAIR pulse sequence in white matter diseases.

Tourbah A, Deschamps R, Stievenart JL, Lopez A, Iba-Zizen MT, Lyon-Caen O, Cabanis EA. Tourbah A, et al. J Neuroradiol. 1996 Dec;23(4):217-22. J Neuroradiol. 1996. PMID: 9107108

8

[Multiple sclerosis. Magnetic resonance imaging and spectroscopy].

Cabanis EA, Tourbah A, Iba-Zizen MT, Stievenart JL, Lyon-Caen O. Cabanis EA, et al. Presse Med. 1997 Oct 25;26(32):1547-53. Presse Med. 1997. PMID: 9435839 Review. French. No abstract available.

9

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

10

[Clinical, biological and neuroradiological aspects of Sneddon's syndrome: 26 cases].

Tourbah A, Piette JC, Benoît N, Iba-Zizen MT, Lyon-Caen O, Francès C. Tourbah A, et al. Rev Neurol (Paris). 1997 Nov;153(11):652-8. Rev Neurol (Paris). 1997. PMID: 9686252 French.

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