(Q30573394)

25 June 2017

title

CADASIL: a review with proposed diagnostic criteria (English)

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25 June 2017

Davous P

1

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25 June 2017

publication date

1 May 1998

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European Journal of Neurology

25 June 2017

published in

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25 June 2017

volume

5

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25 June 2017

issue

3

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25 June 2017

page(s)

219-233

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Binswanger's disease: a review

25 June 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Autosomal dominant leukoencephalopathy and subcortical ischemic stroke. A clinicopathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Summary of the proceedings of the First International Workshop on CADASIL. Paris, May 19-21, 1993.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Progress in the genetics of cerebrovascular disease: inherited subcortical arteriopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Binswanger's disease--revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Sclerosing vasculopathy of the central nervous system in nonelderly demented patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Medullary arteries in aging and dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Small arterial granular degeneration in familial Binswanger's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Pain in Guillain-Barré syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

A gene for familial hemiplegic migraine maps to chromosome 19

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Clinicopathological and genetic studies of two further Italian families with cerebral autosomal dominant arteriopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Senile dementia of the Binswanger type. A vascular form of dementia in the elderly

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

Cerebrotendinous xanthomatosis: molecular diagnosis enables presymptomatic detection of a treatable disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1468-1331.1998.530219.X

10.1046/J.1468-1331.1998.530219.X

21 January 2018

Identifiers

DOI

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25 June 2017

1 reference