Is inadequate family history a barrier to diagnosis in CADASIL? (Q36283775)

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7 January 2020

title

Is inadequate family history a barrier to diagnosis in CADASIL? (English)

1 reference

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7 January 2020

4

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7 January 2020

author name string

Razvi SS

series ordinal

1

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7 January 2020

Davidson R

series ordinal

2

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7 January 2020

Bone I

series ordinal

3

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7 January 2020

language of work or name

English

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publication date

1 November 2005

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Acta Neurologica Scandinavica

7 January 2020

published in

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7 January 2020

volume

112

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7 January 2020

issue

5

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7 January 2020

page(s)

323-326

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

7 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.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/10.1111%2FJ.1600-0404.2005.00495.X

Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X

The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X

De novo mutation in the Notch3 gene causing CADASIL

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1600-0404.2005.00495.X

10.1111/J.1600-0404.2005.00495.X

21 January 2018

Identifiers

DOI

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7 January 2020

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