These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
42. Nonsurgical treatment of cerebral ischemia associated with ACTA2 cerebral arteriopathy: a case report and literature review. Muroi A; Shiono J; Ihara S; Morisaki H; Nakai Y Childs Nerv Syst; 2022 Jun; 38(6):1209-1212. PubMed ID: 34546411 [TBL] [Abstract][Full Text] [Related]
43. "Twig-like" cerebral vessels are not pathognomonic for ACTA A2 mutations: A case report. Nagarajan K; Swamiappan E; Anbazhagan S; Dalal A; Adithan S; Krings T Interv Neuroradiol; 2018 Aug; 24(4):463-468. PubMed ID: 29591721 [TBL] [Abstract][Full Text] [Related]
44. Neonatal diagnosis of ACTA2-related disease: A case report and review of literature. Lupo V; Di Gregorio MG; Mastrogiorgio G; Magliozzi M; Scapillati ME; Maglione V; Romanelli E; Alegiani C; Haass C; Novelli A Am J Med Genet A; 2023 Apr; 191(4):1111-1118. PubMed ID: 36607831 [TBL] [Abstract][Full Text] [Related]
48. Congenital heart defects are rarely caused by mutations in cardiac and smooth muscle actin genes. Khodyuchenko T; Zlotina A; Pervunina T; Zverev D; Malashicheva A; Kostareva A Biomed Res Int; 2015; 2015():127807. PubMed ID: 25861618 [TBL] [Abstract][Full Text] [Related]
49. A familial missense ACTA2 variant p.Arg198Cys leading to Moyamoya-like arteriopathy with straight course of the intracranial arteries, aortic aneurysm and lethal aortic dissection. Focke JK; Kraemer M Neurol Res Pract; 2023 Aug; 5(1):38. PubMed ID: 37587538 [TBL] [Abstract][Full Text] [Related]
50. Mutation of ACTA2 gene as an important cause of familial and nonfamilial nonsyndromatic thoracic aortic aneurysm and/or dissection (TAAD). Morisaki H; Akutsu K; Ogino H; Kondo N; Yamanaka I; Tsutsumi Y; Yoshimuta T; Okajima T; Matsuda H; Minatoya K; Sasaki H; Tanaka H; Ishibashi-Ueda H; Morisaki T Hum Mutat; 2009 Oct; 30(10):1406-11. PubMed ID: 19639654 [TBL] [Abstract][Full Text] [Related]
55. Cerebral arteriopathy and ischemic stroke in a pediatric MYH11 patient. Raghuram A; Sanchez S; Lu Y; Hickerson M; Mayorga MBS; Romero JM; Matsumoto S; Musolino PL; Samaniego EA J Stroke Cerebrovasc Dis; 2023 Mar; 32(3):106938. PubMed ID: 36621119 [TBL] [Abstract][Full Text] [Related]
56. Iris Flocculi as an ocular marker of ACTA2 mutation in familial thoracic aortic aneurysms and dissections. Chamney S; McGimpsey S; McConnell V; Willoughby CE Ophthalmic Genet; 2015 Mar; 36(1):86-8. PubMed ID: 24020716 [TBL] [Abstract][Full Text] [Related]
57. Histopathologic features of intracranial vascular involvement in fibromuscular dysplasia, ehlers-danlos type IV, and neurofibromatosis I. Lummus S; Breeze R; Lucia MS; Kleinschmidt-DeMasters BK J Neuropathol Exp Neurol; 2014 Oct; 73(10):916-32. PubMed ID: 25192048 [TBL] [Abstract][Full Text] [Related]
59. Multisystem smooth muscle dysfunction syndrome in a Chinese girl: A case report and review of the literature. Chen SN; Wang YQ; Hao CL; Lu YH; Jiang WJ; Gao CY; Wu M World J Clin Cases; 2019 Dec; 7(24):4355-4365. PubMed ID: 31911919 [TBL] [Abstract][Full Text] [Related]
60. Structure of the F-actin-tropomyosin complex. von der Ecken J; Müller M; Lehman W; Manstein DJ; Penczek PA; Raunser S Nature; 2015 Mar; 519(7541):114-7. PubMed ID: 25470062 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]