(Q33734810)

29 July 2017

New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature (English)

1 reference

29 July 2017

1 reference

1 reference

Vérin M

1

1 reference

29 July 2017

Rolland Y

2

1 reference

29 July 2017

Landgraf F

3

1 reference

29 July 2017

Chabriat H

4

1 reference

29 July 2017

Bompais B

5

1 reference

29 July 2017

Michel A

6

1 reference

29 July 2017

Vahedi K

7

1 reference

29 July 2017

Martinet JP

8

1 reference

29 July 2017

Tournier-Lasserve E

9

1 reference

29 July 2017

Lemaitre MH

10

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 December 1995

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

29 July 2017

1 reference

29 July 2017

59

1 reference

29 July 2017

6

1 reference

29 July 2017

579-585

1 reference

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

29 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

A gene for familial hemiplegic migraine maps to chromosome 19

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

Progress in the genetics of cerebrovascular disease: inherited subcortical arteriopathies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

Mania after brain injury: neuroradiological and metabolic 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=1073751

Autosomal dominant syndrome with strokelike episodes 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=1073751

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

A familial disorder with subcortical ischemic strokes, dementia, 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=1073751

A second-generation linkage map of the human genome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

Hereditary multi-infarct 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=1073751

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1073751

Hereditary multi-infarct dementia

30 October 2018

1 reference

12 December 2020

Familial subcortical dementia with arteriopathic leukoencephalopathy. A clinico-pathological case

1 reference

12 December 2020

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family

1 reference

12 December 2020

Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus

1 reference

12 December 2020

Chronic familial vascular encephalopathy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.59.6.579

1 reference

29 July 2017

1 reference

29 July 2017

1 reference