(Q30498766)

English

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression

scientific article

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy syndrome mutations increase susceptibility to spreading depression (English)

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

6

object named as

Cenk Ayata

0 references

Katharina Eikermann-Haerter

1

object named as

Katharina Eikermann-Haerter

0 references

object named as

Anne Joutel

4

0 references

author name string

Katharina Eikermann-Haerter

1

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Izumi Yuzawa

2

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Ergin Dilekoz

3

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Michael A Moskowitz

5

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

language of work or name

0 references

publication date

1 February 2011

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Annals of Neurology

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

69

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

413-418

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

Migraine aura pathophysiology: the role of blood vessels and microembolisation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Perfusion pressure-dependent recovery of cortical spreading depression is independent of tissue oxygenation over a wide physiologic range

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Linking Notch signaling to ischemic stroke

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Notch3 is required for arterial identity and maturation of vascular smooth muscle cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Pronounced hypoperfusion during spreading depression in mouse cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

White matter lesions and glial activation in a novel mouse model of chronic cerebral hypoperfusion

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Laser speckle flowmetry for the study of cerebrovascular physiology in normal and ischemic mouse cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

"CADASIL coma": an underdiagnosed acute encephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Reduced cerebrovascular CO(2) reactivity in CADASIL: A transcranial Doppler sonography study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

Cerebral hemodynamics in CADASIL before and after acetazolamide challenge assessed with MRI bolus tracking

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3058390

20 June 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FANA.22281

21 January 2018

The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivo

1 reference

https://api.crossref.org/works/10.1002%2FANA.22281

21 January 2018

Migraine With Aura and Brain Magnetic Resonance Imaging Abnormalities in Patients With CADASIL

1 reference

https://api.crossref.org/works/10.1002%2FANA.22281

21 January 2018

Reversible coma with raised intracranial pressure: an unusual clinical manifestation of CADASIL

1 reference

https://pubmed.ncbi.nlm.nih.gov/21387384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotypic spectrum of CADASIL: clinical findings in 102 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/21387384

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1002/ANA.22281

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 October 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q30498766&oldid=1974480123"