(Q36879466)

English

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family

scientific article published on August 1, 1995

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scholarly article

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Europe PubMed Central

PMC publication ID

16 August 2017

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a clinicopathological and genetic study of a Swiss family (English)

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

Claudio L Bassetti

2

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C. Bassetti

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

Elisabeth Tournier-Lasserve

3

object named as

E. Tournier-Lasserve

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

author name string

H. H. Jung

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

K. Vahedi

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

M. Arnaboldi

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

V. B. Arifi

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

J. M. Burgunder

7

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

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publication date

1 August 1995

1 reference

Europe PubMed Central

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16 August 2017

full work available at URL

https://jnnp.bmj.com/content/jnnp/59/2/138.full.pdf

Portable Document Format

online access status

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

https://europepmc.org/articles/PMC485988

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

https://europepmc.org/articles/PMC485988?pdf=render

Portable Document Format

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7629527

21 June 2024

https://syndication.highwire.org/content/doi/10.1136/jnnp.59.2.138

1 reference

10.1136/JNNP.59.2.138

https://api.crossref.org/works/10.1136/JNNP.59.2.138

21 June 2024

Journal of Neurology, Neurosurgery and Psychiatry

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

59

1 reference

Europe PubMed Central

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16 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

138-143

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

29 September 2017

A gene for familial hemiplegic migraine maps to chromosome 19

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

29 September 2017

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

29 September 2017

Mendelian etiologies of stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

29 September 2017

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

29 September 2017

Autosomal dominant arteriopathic leuko-encephalopathy and Alzheimer's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

Small arterial granular degeneration in familial Binswanger's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

27 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

4 September 2018

Criteria for the diagnosis of ischemic vascular dementia proposed by the State of California Alzheimer's Disease Diagnostic and Treatment Centers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=485988

4 September 2018

Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Familial hemiplegic migraine. Localization of a responsible gene on chromosome 19]

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chronic familial vascular encephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary multi-infarct dementia

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Juvenile arteriosclerotic leukoencephalopathy: anatomoclinical study of a case

1 reference

https://pubmed.ncbi.nlm.nih.gov/7629527

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant syndrome with strokelike episodes and leukoencephalopathy.

10

1 reference

10.1136/JNNP.59.2.138

https://api.crossref.org/works/10.1136/JNNP.59.2.138

21 June 2024

Chronic familial cerebral vasculopathy with peripheral blood lymphocyte abnormalities

22

1 reference

10.1136/JNNP.59.2.138

https://api.crossref.org/works/10.1136/JNNP.59.2.138

21 June 2024

Identifiers

10.1136/JNNP.59.2.138

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

16 August 2017

ResearchGate publication ID

0 references

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