Analysis of ACTA2 in European Moyamoya disease patients-Reference-Cited by-同舟云学术

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Analysis of ACTA2 in European Moyamoya disease patients

Published:2011-03 Issue:2 Volume:15 Page:117-122
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Roder Constantin,Peters Vera,Kasuya Hidetoshi,Nishizawa Tsutomu,Wakita Sho,Berg Daniela,Schulte Claudia,Khan Nadia,Tatagiba Marcos,Krischek Boris

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Cerebrovascular “Moyamoya” Disease. Disease showing abnormal net-like vessels in base of brain;Suzuki;Arch Neurol,1969

2. Genetics of Moyamoya disease;Roder;J Hum Genet,2010

3. Genetic basis of thoracic aortic aneurysms and dissections: focus on smooth muscle cell contractile dysfunction;Milewicz;Annu Rev Genomics Hum Genet,2008

4. Moyamoya disease and Moyamoya syndrome;Scott;N Engl J Med,2009

5. Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease;Guo;Am J Hum Genet,2009

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3. Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations;Nature Communications;2023-11-17

4. Physiological and pathophysiological mechanisms of the molecular and cellular biology of angiogenesis and inflammation in moyamoya angiopathy and related vascular diseases;Frontiers in Neurology;2023-05-16

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