(Q34295928)

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

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Europe PubMed Central

1 August 2017

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

1 reference

Europe PubMed Central

1 August 2017

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A Joutel

4

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H Chabriat

1

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Europe PubMed Central

1 August 2017

K Vahedi

2

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Europe PubMed Central

1 August 2017

M T Iba-Zizen

3

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Europe PubMed Central

1 August 2017

A Nibbio

5

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Europe PubMed Central

1 August 2017

T G Nagy

6

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Europe PubMed Central

1 August 2017

M O Krebs

7

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Europe PubMed Central

1 August 2017

J Julien

8

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Europe PubMed Central

1 August 2017

B Dubois

9

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1 August 2017

X Ducrocq

10

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1 August 2017

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1 October 1995

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Europe PubMed Central

1 August 2017

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Europe PubMed Central

1 August 2017

346

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Europe PubMed Central

1 August 2017

934-939

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Europe PubMed Central

1 August 2017

8980

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Europe PubMed Central

1 August 2017

Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease.

1 reference

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Chronic familial vascular encephalopathy

1 reference

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7 January 2021

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Hereditary multi-infarct dementia

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2991557-5

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based on heuristic

inferred from DOI database lookup

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

1 reference

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7 January 2021

based on heuristic

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A familial disorder with subcortical ischemic strokes, dementia, and leukoencephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2991557-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Slowly progressive familial dementia with recurrent strokes and white matter hypodensities on CT scan.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2991557-5

7 January 2021

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inferred from DOI database lookup

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

1 reference

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

1 reference

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7 January 2021

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A second-generation linkage map of the human genome

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

1 reference

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Reliability of NINDS-AIREN clinical criteria for the diagnosis of vascular dementia.

1 reference

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Symptomatic and nonsymptomatic headaches in a general population

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7 January 2021

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Microinfarction in classic migraine? A study with magnetic resonance imaging findings

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Magnetic resonance imaging of the brain in patients with migraine

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MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

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Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)

1 reference

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The antiphospholipid syndrome: ten years on.

1 reference

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The behavioural and motor consequences of focal lesions of the basal ganglia in man.

1 reference

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Binswanger's disease: a review

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The clinical spectrum of cerebral amyloid angiopathy: presentations without lobar hemorrhage

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7 January 2021

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White matter lesions on magnetic resonance imaging in clinically diagnosed Alzheimer's disease. Evidence for heterogeneity

1 reference

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7 January 2021

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A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2895%2991557-5

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

1 reference

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Identifiers

10.1016/S0140-6736(95)91557-5

1 reference

Europe PubMed Central

1 August 2017

1 reference

Europe PubMed Central

1 August 2017

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