(Q30837377)

13 August 2017

CADASIL in Arabs: clinical and genetic findings (English)

1 reference

13 August 2017

Saeed Bohlega

1

1 reference

13 August 2017

Asmahan Al Shubili

2

1 reference

13 August 2017

Abdulrahman Edris

3

1 reference

13 August 2017

Abdulrahman Alreshaid

4

1 reference

13 August 2017

Thamer Alkhairallah

5

1 reference

13 August 2017

M Walid AlSous

6

1 reference

13 August 2017

Samir Farah

7

1 reference

13 August 2017

Khaled K Abu-Amero

8

1 reference

13 August 2017

9 November 2007

1 reference

13 August 2017

1 reference

13 August 2017

8

1 reference

13 August 2017

67

1 reference

Is inadequate family history a barrier to diagnosis in CADASIL?

13 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

The spectrum of mutations for CADASIL diagnosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

Arg332Cys mutation of NOTCH3 gene in the first known Taiwanese family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

Update on the genetics of stroke and cerebrovascular disease 2004.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

The pathogenesis of CADASIL: an update

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

CADASIL syndrome in a large Turkish kindred caused by the R90C mutation in the Notch3 receptor

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

CADASIL in a North American family: clinical, pathologic, and radiologic findings

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2190758

Human Gene Mutation Database (HGMD): 2003 update

21 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-67

C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-67

Vascular dementia: diagnostic criteria for research studies. Report of the NINDS-AIREN International Workshop

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-67

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: two novel mutations in the NOTCH3 gene in Chinese

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-8-67

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

21 January 2018

1 reference

12 December 2020

The natural history of CADASIL: a pooled analysis of previously published cases

1 reference

12 December 2020

Diagnostic Notch3 sequence analysis in CADASIL: three new mutations in Dutch patients. Dutch CADASIL Research Group

1 reference

12 December 2020

Spectrum of mutations in biopsy-proven CADASIL: implications for diagnostic strategies

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-8-67

1 reference

Dimensions Publication ID

13 August 2017

0 references

1 reference

13 August 2017

PubMed publication ID

17996090

1 reference