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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 11, 2024. (Total: 234259Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Vascular Malformations and ENG[original query]
Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system.
Journal of neurosurgery 2006 Jun 104 (6): 945-9.
Simon Matthias, Franke Daniel, Ludwig Michael, Aliashkevich Ales F, Köster Gertraud, Oldenburg Johannes, Boström Azize, Ziegler Andreas, Schramm Johann
Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia: gene-phenotype correlations.
American journal of medical genetics. Part A 2012 Sep .
Nishida T, Faughnan ME, Krings T, Chakinala M, Gossage JR, Young WL, Kim H, Pourmohamad T, Henderson KJ, Schrum SD, James M, Quinnine N, Bharatha A, Terbrugge KG, White RI
The ACVRL1 c.314-35A>G polymorphism is associated with organ vascular malformations in hereditary hemorrhagic telangiectasia patients with ENG mutations, but not in patients with ACVRL1 mutations.
American journal of medical genetics. Part A 2015 Jun 167 (6): 1262-7.
Pawlikowska Ludmila, Nelson Jeffrey, Guo Diana E, McCulloch Charles E, Lawton Michael T, Young William L, Kim Helen, Faughnan Marie E,
Neurovascular Manifestations of Hereditary Hemorrhagic Telangiectasia: A Consecutive Series of 376 Patients during 15 Years.
AJNR. American journal of neuroradiology 2016 Mar .
Brinjikji W, Iyer V N, Yamaki V, Lanzino G, Cloft H J, Thielen K R, Swanson K L, Wood C
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