Chabriat H - 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. Among authors: chabriat h. Am J Hum Genet. 1996 Jan;58(1):171-81. Am J Hum Genet. 1996. PMID: 8554054 Free PMC article.

2

[Opthalomoplegic migraine].

Chabriat H, Levasseur M, Schaison M, Weiser M, Bousser MG. Chabriat H, et al. Rev Neurol (Paris). 1990;146(11):682-6. Rev Neurol (Paris). 1990. PMID: 2077617 Review. French.

3

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature.

Vérin M, Rolland Y, Landgraf F, Chabriat H, Bompais B, Michel A, Vahedi K, Martinet JP, Tournier-Lasserve E, Lemaitre MH, et al. Vérin M, et al. Among authors: chabriat h. J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):579-85. doi: 10.1136/jnnp.59.6.579. J Neurol Neurosurg Psychiatry. 1995. PMID: 7500094 Free PMC article.

4

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. Lancet. 1995 Oct 7;346(8980):934-9. doi: 10.1016/s0140-6736(95)91557-5. Lancet. 1995. PMID: 7564728

5

An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Ragno M, Tournier-Lasserve E, Fiori MG, Manca A, Patrosso MC, Ferlini A, Sirocchi G, Trojano L, Chabriat H, Salvi F. Ragno M, et al. Among authors: chabriat h. Ann Neurol. 1995 Aug;38(2):231-6. doi: 10.1002/ana.410380216. Ann Neurol. 1995. PMID: 7654071

6

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. Neurology. 1995 Jun;45(6):1086-91. doi: 10.1212/wnl.45.6.1086. Neurology. 1995. PMID: 7783868

7

[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. Among authors: chabriat h. Rev Neurol (Paris). 1994;150(5):340-5. Rev Neurol (Paris). 1994. PMID: 7878319 French.

8

Marchiafava-Bignami disease with dementia: severe cerebral metabolic depression revealed by PET.

Pappata S, Chabriat H, Levasseur M, Legault-Demare F, Baron JC. Pappata S, et al. Among authors: chabriat h. J Neural Transm Park Dis Dement Sect. 1994;8(1-2):131-7. doi: 10.1007/BF02250924. J Neural Transm Park Dis Dement Sect. 1994. PMID: 7893375

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. Among authors: chabriat h. Nat Genet. 1993 Sep;5(1):40-5. doi: 10.1038/ng0993-40. Nat Genet. 1993. PMID: 8220421

10

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.

Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, et al. Tournier-Lasserve E, et al. Among authors: chabriat h. Nat Genet. 1993 Mar;3(3):256-9. doi: 10.1038/ng0393-256. Nat Genet. 1993. PMID: 8485581

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