(Q36143199)

12 August 2017

Inheritance pattern of familial moyamoya disease: autosomal dominant mode and genomic imprinting (English)

1 reference

12 August 2017

1 reference

Y Mineharu

1

1 reference

12 August 2017

K Takenaka

2

1 reference

12 August 2017

H Yamakawa

3

1 reference

12 August 2017

K Inoue

4

1 reference

12 August 2017

H Ikeda

5

1 reference

12 August 2017

K-I Kikuta

6

1 reference

12 August 2017

Y Takagi

7

1 reference

12 August 2017

K Nozaki

8

1 reference

12 August 2017

N Hashimoto

9

1 reference

12 August 2017

A Koizumi

10

1 reference

12 August 2017

language of work or name

English

0 references

publication date

20 June 2006

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

12 August 2017

1 reference

12 August 2017

77

1 reference

12 August 2017

9

1 reference

12 August 2017

1025-1029

1 reference

Adult unilateral moyamoya disease with familial occurrence in two definite cases: a case report and review of the literature

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Epigenetics: regulation through repression

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Familial occurrence of moyamoya disease: a clinical study.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Familial Association of Basilar Bifurcation Aneurysm and Moyamoya Disease-Four Case Reports-

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis ('moyamoya' disease). Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare, Japan

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Noonan syndrome and moyamoya.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Moyamoya disease associated with persistent primitive trigeminal artery variant in identical twins.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2077755

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

23 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

A novel susceptibility locus for moyamoya disease on chromosome 8q23

1 reference

12 December 2020

Moyamoya disease in monovular twins: case report

1 reference

12 December 2020

["Moyamoya" disease found in identical twins (author's transl)]

1 reference

12 December 2020

[Adult identical twins with moyamoya disease]

1 reference

12 December 2020

[Moyamoya disease in twins]

1 reference

12 December 2020

[Moyamoya disease in fraternal twins]

1 reference

12 December 2020

Familial occurrence of moyamoya disease. Magnetic resonance angiography as a screening test for high-risk subjects

1 reference

12 December 2020

Follow-up study of patients with "unilateral" moyamoya disease

1 reference

12 December 2020

[A case of Prader-Willi syndrome with bilateral middle cerebral artery occlusion and moyamoya phenomenon]

1 reference

12 December 2020

The twinning rates by zygosity in Japan, 1975-1994

1 reference

12 December 2020

Moyamoya disease in Europe, past and present status

1 reference

12 December 2020

Genome-wide scan for Japanese familial intracranial aneurysms: linkage to several chromosomal regions

1 reference

12 December 2020

Search on chromosome 17 centromere reveals TNFRSF13B as a susceptibility gene for intracranial aneurysm: a preliminary study

1 reference

12 December 2020

Association analysis of common variants of ELN, NOS2A, APOE and ACE2 to intracranial aneurysm

1 reference

12 December 2020

Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease

1 reference

12 December 2020

Linkage analysis of moyamoya disease on chromosome 6

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.2006.096040

1 reference

12 August 2017

1 reference

12 August 2017

1 reference