Indirect and direct revascularization of ACTA2 cerebral arteriopathy: feasibility of the superficial temporal artery to anterior cerebral artery bypass with posterior auricular artery interposition graft: case report

ACTA2mutation with childhood cardiovascular, autonomic and brain anomalies and severe outcome

(2013) Marije E.C. Meuwissen et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

ACTA2 is not a Major Genetic Risk Gene for Chinese Patients with Moyamoya Disease

(2013) Fa-Yun Hu et al.   International Journal of Stroke

Cerebral arteriopathy associated with Arg179His ACTA2 mutation

(2013) Matthew R Amans et al.   Journal of NeuroInterventional Surgery

A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations

(2012) P. Munot et al.   BRAIN

Neonatal Stroke and Progressive Leukoencephalopathy in a Child With an ACTA2 Mutation

(2012) Ahsan N.V. Moosa et al.   JOURNAL OF CHILD NEUROLOGY

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

Analysis of ACTA2 in European Moyamoya disease patients

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

ACTA2 is not a major disease-causing gene for moyamoya disease

(2009) Keiko Shimojima et al.   JOURNAL OF HUMAN GENETICS

Clinical outcome after 450 revascularization procedures for moyamoya disease

(2009) Raphael Guzman et al.   JOURNAL OF NEUROSURGERY