Inheritance of moyamoya disease in a Caucasian family

Loss of BRCC3 Deubiquitinating Enzyme Leads to Abnormal Angiogenesis and Is Associated with Syndromic Moyamoya

(2011) Snaigune Miskinyte et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients

(2010) Constantin Roder et al.   ACTA NEUROCHIRURGICA

De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction

(2010) Dianna M. Milewicz et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Common genetic polymorphisms in Moyamoya and atherosclerotic disease in Europeans

(2010) Constantin Roder et al.   CHILDS NERVOUS SYSTEM

Analysis of ACTA2 in European Moyamoya disease patients

(2010) Constantin Roder et al.   EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY

Genetics of Moyamoya disease

(2010) Constantin Roder et al.   JOURNAL OF HUMAN GENETICS

A hereditary moyamoya syndrome with multisystemic manifestations

(2010) D. Herve et al.   NEUROLOGY

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

Primary central nervous system vasculitis and moyamoya disease: similarities and differences

(2009) Markus Kraemer et al.   JOURNAL OF NEUROLOGY

Pathophysiology and genetic factors in moyamoya disease

(2009) Achal S. Achrol et al.   Neurosurgical Focus

Autosomal dominant moyamoya disease maps to chromosome 17q25.3

(2008) Y. Mineharu et al.   NEUROLOGY

Moyamoya Disease in Europeans

(2008) Markus Kraemer et al.   STROKE