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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Hemorrhage and ACVRL1[original query]
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
Replication Study of Polymorphisms Associated With Brain Arteriovenous Malformation in a Population From South of Brazil.
Cureus 2016 Feb 8 (2): e508.
Franciscatto André Cerutti, Ludwig Fernanda S, Matte Ursula S, Mota Simone, Stefani Marco
[Gene Analysis of A Chinese Family with Hereditary Hemorrhagic Telangiectasia and its Curative Effect of Thalidomide].
Zhongguo shi yan xue ye xue za zhi 2017 8 25 (4): 1136-1141.
Yu Qian, Cheng Zhao, Yi Yi-Fang, Peng Hong-Li
Clinical and genetic findings in children with central nervous system arteriovenous fistulas.
Annals of neurology 2017 11 82 (6): 972-980.
Saliou Guillaume, Eyries Mélanie, Iacobucci Marta, Knebel Jean-François, Waill Marie-Christine, Coulet Florence, Ozanne Augustin, Soubrier Flore
Pulmonary Hypertension and Hereditary Hemorrhagic Telangiectasia Related to an ACVRL1 Mutation.
Internal medicine (Tokyo, Japan) 2019 9 59 (2): 221-227.
Yokokawa Tetsuro, Sugimoto Koichi, Kimishima Yusuke, Misaka Tomofumi, Yoshihisa Akiomi, Morisaki Hiroko, Yamada Osamu, Nakazato Kazuhiko, Ishida Takafumi, Takeishi Yasuchi
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