(Q51838971)

13 April 2018

title

Clinical features of familial moyamoya disease. (English)

1 reference

13 April 2018

author name string

Rina Nanba

1

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13 April 2018

Satoshi Kuroda

2

1 reference

13 April 2018

Mitsuhiro Tada

3

1 reference

13 April 2018

Tatsuya Ishikawa

4

1 reference

13 April 2018

Kiyohiro Houkin

5

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13 April 2018

Yoshinobu Iwasaki

6

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13 April 2018

publication date

30 September 2005

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13 April 2018

published in

Child's Nervous System

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13 April 2018

volume

22

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13 April 2018

page(s)

258-262

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13 April 2018

issue

3

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13 April 2018

https://scigraph.springernature.com/pub.10.1007/s00381-005-1230-5

exact match

0 references

cites work

Cerebrovascular "moyamoya" disease. Disease showing abnormal net-like vessels in base of brain.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00381-005-1230-5

Linkage of Familial Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis) to Chromosome 17q25

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00381-005-1230-5

Familial occurrence of moyamoya disease in the mother and four daughters including identical twins

21 January 2018

1 reference

12 December 2020

Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey.

1 reference

12 December 2020

Familial intracranial aneurysms

1 reference

12 December 2020

Clinical observations on familial cluster headache

1 reference

12 December 2020

Worldwide Distribution of Moyamoya Disease

1 reference

12 December 2020

A survey of moyamoya disease in Hawaii

1 reference

12 December 2020

Familial subarachnoid hemorrhage: distinctive features and patterns of inheritance.

1 reference

12 December 2020

Trinucleotide repeats not the only cause of anticipation.

1 reference

12 December 2020

Linkage analysis of moyamoya disease on chromosome 6

1 reference

12 December 2020

Intracranial aneurysms and heredity

1 reference

12 December 2020

Angiogenic factors in moyamoya disease

1 reference

12 December 2020

Familial occurrence of moyamoya disease

1 reference

12 December 2020

Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

1 reference

12 December 2020

A comparison of familial and sporadic migraine in a headache clinic population

1 reference

12 December 2020

Epigenetics: interaction of DNA methylation and chromatin

1 reference

12 December 2020

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

1 reference

12 December 2020

The cerebrospinal fluid in patients with moyamoya disease (spontaneous occlusion of the circle of Willis) contains high level of basic fibroblast growth factor

1 reference

12 December 2020

[Familial moyamoya disease--clinical features and current study]

1 reference

12 December 2020

The relationship between moyamoya disease and bacterial infection

1 reference

12 December 2020

Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26.

1 reference

12 December 2020

Trinucleotide repeat expansion and human disease

1 reference

12 December 2020

Genomic imprinting: review and relevance to human diseases.

1 reference

12 December 2020

Sequence analysis and bioinformatics analysis of chromosome 17q25 in familial moyamoya disease.

1 reference

12 December 2020

10.1007/S00381-005-1230-5

Identifiers

DOI

1 reference

13 April 2018

PubMed ID

16195874

1 reference

13 April 2018