Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease
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Title
Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease
Authors
Keywords
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Journal
JOURNAL OF NEUROSURGERY
Volume 124, Issue 5, Pages 1221-1227
Publisher
Journal of Neurosurgery Publishing Group (JNSPG)
Online
2015-10-02
DOI
10.3171/2015.4.jns142900
References
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Note: Only part of the references are listed.- Distribution of Moyamoya Disease Susceptibility Polymorphism p.R4810K in RNF213 in East and Southeast Asian Populations
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- 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
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- (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
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