Maki Mukawa

Tokyo, Japan

Last Updated: 09/26/2026

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Found 14 publications

Two Postmortem Cases of Moyamoya Disease with Different RNF213 p.R4810K Variant Statuses.

Two Postmortem Cases of Moyamoya Disease with Different RNF213 p.R4810K Variant Statuses.

Journal: NMC case report journal

Published: June 12, 2024

Changes in the clinical spectrum of pediatric moyamoya disease over 40 years.

Changes in the clinical spectrum of pediatric moyamoya disease over 40 years.

Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery

Published: June 09, 2022

Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients.

Absence of the RNF213 p.R4810K variant may indicate a severe form of pediatric moyamoya disease in Japanese patients.

Journal: Journal of neurosurgery. Pediatrics

Published: May 14, 2021

Clinical characteristics of the pregnancies and deliveries of patients with moyamoya disease: A single-center analysis over three decades.

Clinical characteristics of the pregnancies and deliveries of patients with moyamoya disease: A single-center analysis over three decades.

Journal: International journal of stroke : official journal of the International Stroke Society

Published: October 12, 2020

Rare and Low-Frequency Variants in RNF213 Confer Susceptibility to Moyamoya Syndrome Associated with Hyperthyroidism.

Rare and Low-Frequency Variants in RNF213 Confer Susceptibility to Moyamoya Syndrome Associated with Hyperthyroidism.

Journal: World neurosurgery

Published: November 03, 2018

Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease.

Novel and recurrent RNF213 variants in Japanese pediatric patients with moyamoya disease.

Journal: Human genome variation

Published: September 16, 2017

Case of Familial Moyamoya Disease Presenting 10 Years After Initial Negative Magnetic Resonance Screening in Childhood.

Case of Familial Moyamoya Disease Presenting 10 Years After Initial Negative Magnetic Resonance Screening in Childhood.

Journal: World neurosurgery

Published: April 15, 2017

Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease.

Exome Sequencing Identified CCER2 as a Novel Candidate Gene for Moyamoya Disease.

Journal: Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association

Published: May 31, 2016

First autopsy analysis of a neovascularized arterial network induced by indirect bypass surgery for moyamoya disease: case report.

First autopsy analysis of a neovascularized arterial network induced by indirect bypass surgery for moyamoya disease: case report.

Journal: Journal of neurosurgery

Published: September 26, 2015

Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.

Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.

Journal: Journal of the American Heart Association

Published: May 13, 2015

Practical clinical use of dynamic susceptibility contrast magnetic resonance imaging for the surgical treatment of moyamoya disease.

Practical clinical use of dynamic susceptibility contrast magnetic resonance imaging for the surgical treatment of moyamoya disease.

Journal: Neurosurgery

Published: December 17, 2013

Successful coil embolization of a ruptured basilar artery aneurysm in a child with leukemia: a case report.

Successful coil embolization of a ruptured basilar artery aneurysm in a child with leukemia: a case report.

Journal: Neurologia medico-chirurgica

Published: November 22, 2013

Showing 1-12 of 14

Last Updated: 09/26/2026