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Results: 1 to 20 of 394

Similar articles for PubMed (Select 7564728)

1.

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.

Lancet. 1995 Oct 7;346(8980):934-9.

PMID:
7564728
2.

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.

J Neurol Neurosurg Psychiatry. 1995 Dec;59(6):579-85.

3.

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.

Neurology. 1995 Jun;45(6):1086-91.

PMID:
7783868
4.

SPECT study of a German CADASIL family: a phenotype with migraine and progressive dementia only.

Mellies JK, Bäumer T, Müller JA, Tournier-Lasserve E, Chabriat H, Knobloch O, Hackelöer HJ, Goebel HH, Wetzig L, Haller P.

Neurology. 1998 Jun;50(6):1715-21.

PMID:
9633716
5.

[CADASIS. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalophathy].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

Rev Neurol (Paris). 1997 Jul;153(6-7):376-85. Review. French.

PMID:
9684003
6.

Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL).

Hutchinson M, O'Riordan J, Javed M, Quin E, Macerlaine D, Wilcox T, Parfrey N, Nagy TG, Tournier-Lasserve E.

Ann Neurol. 1995 Nov;38(5):817-24.

PMID:
7486874
8.

[Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia].

Lopera F, Arboleda J, Moreno S, Almeida N, Cuartas M, Arcos-Burgos M.

Rev Neurol. 2000 Nov 16-30;31(10):901-7. Spanish.

PMID:
11244680
9.

Unusual clinical features and early brain MRI lesions in a family with cerebral autosomal dominant arteriopathy.

Malandrini A, Carrera P, Ciacci G, Gonnelli S, Villanova M, Palmeri S, Vismara L, Brancolini V, Signorini E, Ferrari M, Guazzi GC.

Neurology. 1997 May;48(5):1200-3.

PMID:
9153443
10.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family.

Jung HH, Bassetti C, Tournier-Lasserve E, Vahedi K, Arnaboldi M, Arifi VB, Burgunder JM.

J Neurol Neurosurg Psychiatry. 1995 Aug;59(2):138-43.

12.

[Hereditary CADASIL cerebral arteriopathy. Report of a family].

Mayer M, Dichgans M, Gasser T, Büttner U, Uttner I, Straube A.

Nervenarzt. 1995 Dec;66(12):927-32. German.

PMID:
8584078
13.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family.

Sabbadini G, Francia A, Calandriello L, Di Biasi C, Trasimeni G, Gualdi GF, Palladini G, Manfredi M, Frontali M.

Brain. 1995 Feb;118 ( Pt 1):207-15.

PMID:
7895005
14.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR findings.

Skehan SJ, Hutchinson M, MacErlaine DP.

AJNR Am J Neuroradiol. 1995 Nov-Dec;16(10):2115-9.

15.

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.

Ann Neurol. 1995 Aug;38(2):231-6. Erratum in: Ann Neurol. 2012 Jun;71(6):854.

PMID:
7654071
16.

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

J Mal Vasc. 1996;21(5):277-82. Review. French.

PMID:
9026542
17.

[CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): clinical features and neuroimaging].

Chabriat H, Joutel A, Vahedi K, Iba-Zizen MT, Tournier-Lasserve E, Bousser MG.

Bull Acad Natl Med. 2000;184(7):1523-31; discussion 1531-3. Review. French.

PMID:
11261256
18.

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.

Nat Genet. 1993 Mar;3(3):256-9.

PMID:
8485581
19.
20.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Lesnik Oberstein SA, Haan J.

Panminerva Med. 2004 Dec;46(4):265-76. Review.

PMID:
15876982
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