Literature DB >> 69080

Chronic familial vascular encephalopathy.

D L Stevens, R H Hewlett, B Brownell.   

Abstract

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Year:  1977        PMID： 69080     DOI： 10.1016/s0140-6736(77)92576-4

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  12 in total

Review 1.  Single gene disorders causing ischaemic stroke.

Authors:  Saif S M Razvi; Ian Bone
Journal:  J Neurol       Date:  2006-06       Impact factor: 4.849

2.  Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity.

Authors:  D St Clair; J Bolt; S Morris; D Doyle
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

3.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease.

Authors:  Jay Chol Choi
Journal:  J Clin Neurol       Date:  2010-03-26       Impact factor: 3.077

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

Authors:  M Vérin; Y Rolland; F Landgraf; H Chabriat; B Bompais; A Michel; K Vahedi; J P Martinet; E Tournier-Lasserve; M H Lemaitre
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-12       Impact factor: 10.154

5.  Small arterial granular degeneration in familial Binswanger's syndrome.

Authors:  M Gutiérrez-Molina; A Caminero Rodríguez; C Martínez García; J Arpa Gutiérrez; C Morales Bastos; G Amer
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

6.  Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval.

Authors:  A Ducros; T Nagy; S Alamowitch; A Nibbio; A Joutel; K Vahedi; H Chabriat; M T Iba-Zizen; J Julien; P Davous; J Y Goas; O Lyon-Caen; B Dubois; X Ducrocq; F Salsa; M Ragno; P Burkhard; C Bassetti; M Hutchinson; M Vérin; F Viader; F Chapon; M Levasseur; J L Mas; O Delrieu
Journal:  Am J Hum Genet       Date:  1996-01       Impact factor: 11.025

7.  Identification of the characteristic vascular changes in a sural nerve biopsy of a case with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Authors:  J M Schröder; B Sellhaus; J Jörg
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

8.  Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Authors:  M M Ruchoux; D Guerouaou; B Vandenhaute; J P Pruvo; P Vermersch; D Leys
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

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

Authors:  H H Jung; C Bassetti; E Tournier-Lasserve; K Vahedi; M Arnaboldi; V B Arifi; J M Burgunder
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

10.  The microvascular changes in cases of hereditary multi-infarct disease of the brain.

Authors:  W W Zhang; K C Ma; O Andersen; P Sourander; P O Tollesson; Y Olsson
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088
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