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.
5. Moyamoya disease and syndromes: from genetics to clinical management. Guey S; Tournier-Lasserve E; Hervé D; Kossorotoff M Appl Clin Genet; 2015; 8():49-68. PubMed ID: 25733922 [TBL] [Abstract][Full Text] [Related]
6. De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy. Guey S; Grangeon L; Brunelle F; Bergametti F; Amiel J; Lyonnet S; Delaforge A; Arnould M; Desnous B; Bellesme C; Hervé D; Schwitalla JC; Kraemer M; Tournier-Lasserve E; Kossorotoff M J Med Genet; 2017 Aug; 54(8):550-557. PubMed ID: 28343148 [TBL] [Abstract][Full Text] [Related]
7. Xq28 copy number gain causing moyamoya disease and a novel moyamoya syndrome. Aloui C; Guey S; Pipiras E; Kossorotoff M; Guéden S; Corpechot M; Bessou P; Pedespan JM; Husson M; Hervé D; Riant F; Kraemer M; Steffann J; Quenez O; Tournier-Lasserve E J Med Genet; 2020 May; 57(5):339-346. PubMed ID: 31924698 [TBL] [Abstract][Full Text] [Related]
8. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome. Luisa SF; Rizzo A; Bedini G; Capone F; Di Lazzaro V; Nava S; Acerbi F; Rossi DS; Binelli S; Faragò G; Gioppo A; Grisoli M; Bruzzone MG; Ferroli P; Pantaleoni C; Caputi L; Gomez JV; Parati EA; Bersano A Int J Mol Sci; 2018 Nov; 19(11):. PubMed ID: 30463371 [TBL] [Abstract][Full Text] [Related]
9. Haemophilia A and cardiovascular morbidity in a female SHAM syndrome carrier due to skewed X chromosome inactivation. Janczar S; Kosinska J; Ploski R; Pastorczak A; Wegner O; Zalewska-Szewczyk B; Paige AJ; Borowiec M; Mlynarski W Eur J Med Genet; 2016 Jan; 59(1):43-7. PubMed ID: 26691666 [TBL] [Abstract][Full Text] [Related]
10. Cutaneous manifestations in Moyamoya angiopathy: A review. Mitri F; Bersano A; Hervé D; Kraemer M Eur J Neurol; 2021 May; 28(5):1784-1793. PubMed ID: 33486780 [TBL] [Abstract][Full Text] [Related]
11. Clinical Characteristics of Moyamoya Angiopathy in a Pediatric Cohort. Pines AR; Rodriguez D; Bendok BR; Dhamija R J Child Neurol; 2020 May; 35(6):389-392. PubMed ID: 32089044 [TBL] [Abstract][Full Text] [Related]
12. Pathophysiology and genetic factors in moyamoya disease. Achrol AS; Guzman R; Lee M; Steinberg GK Neurosurg Focus; 2009 Apr; 26(4):E4. PubMed ID: 19335130 [TBL] [Abstract][Full Text] [Related]
15. Whole exome sequencing identifies MRVI1 as a susceptibility gene for moyamoya syndrome in neurofibromatosis type 1. Santoro C; Giugliano T; Kraemer M; Torella A; Schwitalla JC; Cirillo M; Melis D; Berlit P; Nigro V; Perrotta S; Piluso G PLoS One; 2018; 13(7):e0200446. PubMed ID: 30001348 [TBL] [Abstract][Full Text] [Related]
16. Moyamoya disease in two patients with Noonan-like syndrome with loose anagen hair. Lo FS; Wang CJ; Wong MC; Lee NC Am J Med Genet A; 2015 Jun; 167(6):1285-8. PubMed ID: 25858597 [TBL] [Abstract][Full Text] [Related]
17. Moyamoya disease associated with asymptomatic mosaic Turner syndrome: a rare cause of hemorrhagic stroke. Manjila S; Miller BR; Rao-Frisch A; Otvos B; Mitchell A; Bambakidis NC; De Georgia MA J Stroke Cerebrovasc Dis; 2014; 23(5):1242-4. PubMed ID: 24103673 [TBL] [Abstract][Full Text] [Related]
18. Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical features. Bayram AK; Yilmaz E; Per H; Ito M; Uchino H; Doganay S; Houkin K; Unal E Childs Nerv Syst; 2016 Mar; 32(3):569-73. PubMed ID: 26277359 [TBL] [Abstract][Full Text] [Related]
19. [Moyamoya disease]. Tokunaga K; Date I Brain Nerve; 2008 Jan; 60(1):37-42. PubMed ID: 18232331 [TBL] [Abstract][Full Text] [Related]
20. Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association. Toldo I; Po' C; Morao V; Talenti G; Causin F; D'Avella D; Tenconi R; Suppiej A; Sartori S Eur J Paediatr Neurol; 2016 Sep; 20(5):766-71. PubMed ID: 27236536 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]