Joutel A - Search Results

1

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients.

Joutel A, Vahedi K, Corpechot C, Troesch A, Chabriat H, Vayssière C, Cruaud C, Maciazek J, Weissenbach J, Bousser MG, Bach JF, Tournier-Lasserve E. Joutel A, et al. Lancet. 1997 Nov 22;350(9090):1511-5. doi: 10.1016/S0140-6736(97)08083-5. Lancet. 1997. PMID: 9388399

2

Clinical spectrum of CADASIL: a study of 7 families. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Chabriat H, Vahedi K, Iba-Zizen MT, Joutel A, Nibbio A, Nagy TG, Krebs MO, Julien J, Dubois B, Ducrocq X, et al. Chabriat H, et al. Among authors: joutel a. Lancet. 1995 Oct 7;346(8980):934-9. doi: 10.1016/s0140-6736(95)91557-5. Lancet. 1995. PMID: 7564728

3

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.

Vahedi K, Joutel A, Van Bogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Among authors: joutel a. Ann Neurol. 1995 Mar;37(3):289-93. doi: 10.1002/ana.410370304. Ann Neurol. 1995. PMID: 7695228

4

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus.

Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A, et al. Chabriat H, et al. Among authors: joutel a. Neurology. 1995 Jun;45(6):1086-91. doi: 10.1212/wnl.45.6.1086. Neurology. 1995. PMID: 7783868

5

Monozygotic twins discordant for familial hemiplegic migraine.

Ducros A, Joutel A, Labauge P, Pagès M, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Among authors: joutel a. Neurology. 1995 Jun;45(6):1222. doi: 10.1212/wnl.45.6.1222. Neurology. 1995. PMID: 7783896 No abstract available.

6

[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19].

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al. Joutel A, et al. Rev Neurol (Paris). 1994;150(5):340-5. Rev Neurol (Paris). 1994. PMID: 7878319 French.

7

[Hemiplegic migraine].

Joutel A, Tournier-Lasserve E, Bousser MG. Joutel A, et al. Presse Med. 1995 Feb 25;24(8):411-4. Presse Med. 1995. PMID: 7899422 Review. French.

8

Genetic heterogeneity of familial hemiplegic migraine.

Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al. Joutel A, et al. Am J Hum Genet. 1994 Dec;55(6):1166-72. Am J Hum Genet. 1994. PMID: 7977376 Free PMC article.

9

A gene for familial hemiplegic migraine maps to chromosome 19.

Joutel A, Bousser MG, Biousse V, Labauge P, Chabriat H, Nibbio A, Maciazek J, Meyer B, Bach MA, Weissenbach J, et al. Joutel A, et al. Nat Genet. 1993 Sep;5(1):40-5. doi: 10.1038/ng0993-40. Nat Genet. 1993. PMID: 8220421

10

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study.

Baudrimont M, Dubas F, Joutel A, Tournier-Lasserve E, Bousser MG. Baudrimont M, et al. Among authors: joutel a. Stroke. 1993 Jan;24(1):122-5. doi: 10.1161/01.str.24.1.122. Stroke. 1993. PMID: 8418535

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