Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy
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Title
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya Angiopathy
Authors
Keywords
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Journal
STROKE
Volume 50, Issue 4, Pages 789-796
Publisher
Ovid Technologies (Wolters Kluwer Health)
Online
2019-03-14
DOI
10.1161/strokeaha.118.023972
References
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Related references
Note: Only part of the references are listed.- Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians
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- De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy
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- Female mice lacking Pald1 exhibit endothelial cell apoptosis and emphysema
- (2017) Isabel Egaña et al. Scientific Reports
- Headache in Caucasian patients with Moyamoya angiopathy – a systematic cohort study
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- Disrupted nitric oxide signaling due toGUCY1A3mutations increases risk for moyamoya disease, achalasia and hypertension
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- Loss of α1β1 Soluble Guanylate Cyclase, the Major Nitric Oxide Receptor, Leads to Moyamoya and Achalasia
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- Prospective Screening of Family Members with Moyamoya Disease Patients
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- RNF213 Rare Variants in an Ethnically Diverse Population With Moyamoya Disease
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- Disease-targeted sequencing: a cornerstone in the clinic
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- Guidelines for Diagnosis and Treatment of Moyamoya Disease (Spontaneous Occlusion of the Circle of Willis)
- (2013) et al. NEUROLOGIA MEDICO-CHIRURGICA
- Paladin (X99384) is expressed in the vasculature and shifts from endothelial to vascular smooth muscle cells during mouse development
- (2012) Elisabet Wallgard et al. DEVELOPMENTAL DYNAMICS
- Sex Differences in Clinical Presentation and Treatment Outcomes in Moyamoya Disease
- (2012) Nadia Khan et al. NEUROSURGERY
- Characterization of Direct and Indirect Cerebral Revascularization for the Treatment of European Patients with Moyamoya Disease
- (2011) M. Czabanka et al. CEREBROVASCULAR DISEASES
- Inheritance of moyamoya disease in a Caucasian family
- (2011) M. Kraemer et al. EUROPEAN JOURNAL 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
- Bioinformatic identification and characterization of human endothelial cell-restricted genes
- (2010) Manoj Bhasin et al. BMC GENOMICS
- A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
- (2010) Fumiaki Kamada et al. JOURNAL OF HUMAN GENETICS
- Combination of Reverse and Chemical Genetic Screens Reveals Angiogenesis Inhibitors and Targets
- (2009) Mattias Kalén et al. CHEMISTRY & BIOLOGY
- Moyamoya Disease and Moyamoya Syndrome
- (2009) R. Michael Scott et al. NEW ENGLAND JOURNAL OF MEDICINE
- Identification of a Core Set of 58 Gene Transcripts With Broad and Specific Expression in the Microvasculature
- (2008) Elisabet Wallgard et al. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
- Progression of disease in unilateral moyamoya syndrome
- (2008) Edward R. Smith et al. Neurosurgical Focus
- Moyamoya Disease in Europeans
- (2008) Markus Kraemer et al. STROKE
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