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Acta Neuropathologica, ISSN 0001-6322, 05/2018, Volume 135, Issue 5, p. 801
Journal Article
Nature, ISSN 0028-0836, 2013, Volume 498, Issue 7455, pp. 492 - 496
Journal Article
Trends in Molecular Medicine, ISSN 1471-4914, 05/2013, Volume 19, Issue 5, pp. 302 - 308
Cerebral cavernous malformations (CCMs) are vascular lesions that can occur sporadically or as a consequence of inherited loss-of-function mutations,... 
Journal Article
Trends in Molecular Medicine, ISSN 1471-4914, 2013, Volume 19, Issue 5, pp. 302 - 308
Journal Article
Annals of Neurology, ISSN 0364-5134, 03/2000, Volume 47, Issue 3, pp. 388 - 391
CADASIL, an autosomal dominant arteriopathy responsible for stroke and dementia, is caused by strongly stereotyped mutations in the Notch3 gene. We report a... 
Journal Article
Seminars in Cell and Developmental Biology, ISSN 1084-9521, 1998, Volume 9, Issue 6, pp. 619 - 625
Journal Article
Journal Article
Neurosurgery, ISSN 0148-396X, 05/2017, Volume 80, Issue 5, pp. 665 - 680
Journal Article
Application of Clinical Genetics, ISSN 1178-704X, 02/2015, Volume 8, pp. 49 - 68
Moyamoya angiopathy is characterized by a progressive stenosis of the terminal portion of the internal carotid arteries and the development of a network of... 
Moyamoya syndrome | Genetics | Stroke | Moyamoya disease | Surgical revascularization | Care and treatment | Ischemia | Analysis | Diagnostic imaging | Genetic aspects | Diagnosis | Research | Pediatrics | Genetic disorders | Cardiovascular disease | Down syndrome | Hemorrhage | Dwarfism | Ethnicity | Adults | Mutation | Carotid artery | Hyperventilation
Journal Article
Stroke, ISSN 0039-2499, 05/2015, Volume 46, Issue 5, pp. 1337 - 1343
Journal Article