(Q48726586)

15 February 2018

title

Population-specific spectrum of NOTCH3 mutations, MRI features and founder effect of CADASIL in Chinese. (English)

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15 February 2018

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1

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15 February 2018

Jong-Ling Fuh

5

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15 February 2018

author name string

Chin-San Liu

2

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15 February 2018

Ming-Hong Chang

3

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15 February 2018

Kon-Ping Lin

4

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15 February 2018

Yi-Chu Lu

6

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15 February 2018

Ya-Fen Liu

7

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15 February 2018

Bing-Wen Soong

8

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15 February 2018

publication date

26 February 2009

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15 February 2018

published in

Journal of Neurology

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15 February 2018

volume

256

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15 February 2018

issue

2

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15 February 2018

page(s)

249-255

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15 February 2018

https://scigraph.springernature.com/pub.10.1007/s00415-009-0091-3

exact match

0 references

cites work

MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-009-0091-3

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

21 January 2018

1 reference

12 December 2020

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Cerebellar arteriovenous malformation and vertebral artery aneurysm in a CADASIL patient

1 reference

12 December 2020

The spectrum of Notch3 mutations in 28 Italian CADASIL families

1 reference

12 December 2020

1 reference

12 December 2020

Intracerebral hemorrhages in CADASIL.

1 reference

12 December 2020

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]

1 reference

12 December 2020

CADASIL mimicking primary angiitis of the central nervous system.

1 reference

12 December 2020

A semiquantative rating scale for the assessment of signal hyperintensities on magnetic resonance imaging.

1 reference

12 December 2020

Detection of the founder effect in Finnish CADASIL families

1 reference

12 December 2020

Diagnostic strategies in CADASIL

1 reference

12 December 2020

Diagnostic value of ultrastructural skin biopsy studies in CADASIL.

1 reference

12 December 2020

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

1 reference

12 December 2020

Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients

1 reference

12 December 2020

Blood pressure and haemoglobin A1c are associated with microhaemorrhage in CADASIL: a two-centre cohort study.

1 reference

12 December 2020

De novo mutation in the Notch3 gene causing CADASIL

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

1 reference

12 December 2020

Diagnostic strategies in CADASIL

1 reference

12 December 2020

10.1007/S00415-009-0091-3

Identifiers

DOI

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15 February 2018

release_oo5hp7v3ojgszhspoeawpssbya

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/oo5hp7v3ojgszhspoeawpssbya

24 November 2022

mapped directly with Wikidata item

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15 February 2018