Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease

Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations

(2015) Wanyang LIU et al.   NEUROLOGIA MEDICO-CHIRURGICA

Temporal profile of the vascular anatomy evaluated by 9.4-T magnetic resonance angiography and histopathological analysis in mice lacking RNF213: A susceptibility gene for moyamoya disease

(2014) Shinya Sonobe et al.   BRAIN RESEARCH

Rapid Progression of Unilateral Moyamoya Disease in a Patient with a Family History and anRNF213Risk Variant

(2014) Yohei Mineharu et al.   CEREBROVASCULAR DISEASES

Downregulation of Securin by the variant RNF213 R4810K (rs112735431, G>A) reduces angiogenic activity of induced pluripotent stem cell-derived vascular endothelial cells from moyamoya patients

(2013) Toshiaki Hitomi et al.   BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Guidelines for Diagnosis and Treatment of Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis)

(2013) et al.   NEUROLOGIA MEDICO-CHIRURGICA

Homozygous c.l4576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease

(2012) S. Miyatake et al.   NEUROLOGY

Molecular Analysis of RNF213 Gene for Moyamoya Disease in the Chinese Han Population

(2012) Zhiyuan Wu et al.   PLoS One

Acute ischemic stroke in children versus young adults

(2011) Sandra Bigi et al.   ANNALS OF NEUROLOGY

Arterial ischemic stroke risk factors: The international pediatric stroke study

(2011) Mark T. Mackay et al.   ANNALS OF NEUROLOGY

Identification of RNF213 as a Susceptibility Gene for Moyamoya Disease and Its Possible Role in Vascular Development

(2011) Wanyang Liu et al.   PLoS One

Pediatric moyamoya disease: An analysis of 410 consecutive cases

(2010) Seung-Ki Kim et al.   ANNALS OF NEUROLOGY

Association of a Functional Polymorphism in the MMP-3 Gene with Moyamoya Disease in the Chinese Han Population

(2010) Hao Li et al.   CEREBROVASCULAR DISEASES

A genome-wide association study identifies RNF213 as the first Moyamoya disease gene

(2010) Fumiaki Kamada et al.   JOURNAL OF HUMAN GENETICS

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

(2009) Dong-Chuan Guo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Moyamoya Disease and Moyamoya Syndrome

(2009) R. Michael Scott et al.   NEW ENGLAND JOURNAL OF MEDICINE

A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

(2009) Wanyang Liu et al.   Environmental Health and Preventive Medicine

Moyamoya disease: current concepts and future perspectives

(2008) Satoshi Kuroda et al.   LANCET NEUROLOGY

Prevalence and Clinicoepidemiological Features of Moyamoya Disease in Japan

(2007) Shinichi Kuriyama et al.   STROKE