Literature DB >> 67459

Hereditary multi-infarct dementia.

P Sourander, J Wälinder.   

Abstract

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Year:  1977        PMID： 67459     DOI： 10.1016/s0140-6736(77)92324-8

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


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  4 in total

Review 1.  Cerebrovascular disorders associated with genetic lesions.

Authors:  Philipp Karschnia; Sayoko Nishimura; Angeliki Louvi
Journal:  Cell Mol Life Sci       Date:  2018-10-16       Impact factor: 9.261

2.  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

3.  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

4.  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
  4 in total

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