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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 - 8 (of 8 Records)

Query Trace: Syndrome and GPI[original query]
Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.
Human mutation 2004 Dec 24 (6): 534-5.
Sinibaldi Lorenzo, De Luca Alessandro, Bellacchio Emanuele, Conti Emanuela, Pasini Augusto, Paloscia Claudio, Spalletta Gianfranco, Caltagirone Carlo, Pizzuti Antonio, Dallapiccola Bru
Significance of valine/leucine247 polymorphism of beta2-glycoprotein I in antiphospholipid syndrome: increased reactivity of anti-beta2-glycoprotein I autoantibodies to the valine247 beta2-glycoprotein I variant.
Arthritis and rheumatism 2005 Jan 52 (1): 212-8.
Yasuda Shinsuke, Atsumi Tatsuya, Matsuura Eiji, Kaihara Keiko, Yamamoto Daisuke, Ichikawa Kenji, Koike Tak
Val/Leu247 polymorphism of beta2-glycoprotein I in Brazilian patients with antiphospholipid syndrome--a genetic risk factor?
Annals of the New York Academy of Sciences 2009 Sep 1173 509-14.
Pernambuco-Climaco Juliana M, Brochado Maria Jose F, Freitas Max Victor C, Roselino Ana Maria F, Louzada-Junior Pau
Increased warfarin consumption and residual fibrin turnover in thrombotic patients with primary antiphospholipid syndrome.
Thrombosis research 2011 Jun 127 (6): 595-9.
Ames Paul R J, Margaglione Maurizio, Ciampa Antonio, Colaizzo Donatella, Ferrara Felicetto, Iannaccone Luigi, Vincenzobrancacci
Association between the valine/leucine247 polymorphism of ß2-glycoprotein I and susceptibility to anti-phospholipid syndrome: a meta-analysis.
Lupus 2012 Jul 21 (8): 865-71.
Lee Y H, Choi S J, Ji J D, Song G
Val247Leu ß2-glycoprotein-I allelic variant is associated with antiphospholipid syndrome: systematic review and meta-analysis.
Autoimmunity reviews 2012 Aug 11 (10): 705-12.
Chamorro Antonio-Javier, Marcos Miguel, Mirón-Canelo José-Antonio, Cervera Ricard, Espinosa Gera
Anti-citrullinated glucose-6-phosphate isomerase peptide antibodies in patients with rheumatoid arthritis are associated with HLA-DRB1 shared epitope alleles and disease activity.
Clinical and experimental immunology 2013 Apr 172 (1): 1.
Umeda N, Matsumoto I, Ito I, Kawasaki A, Tanaka Y, Inoue A, Tsuboi H, Suzuki T, Hayashi T, Ito S, Tsuchiya N, Sumida T
PIGA mutations cause early-onset epileptic encephalopathies and distinctive features.
Neurology 2014 May 82 (18): 1587-96.
Kato Mitsuhiro, Saitsu Hirotomo, Murakami Yoshiko, Kikuchi Kenjiro, Watanabe Shuei, Iai Mizue, Miya Kazushi, Matsuura Ryuki, Takayama Rumiko, Ohba Chihiro, Nakashima Mitsuko, Tsurusaki Yoshinori, Miyake Noriko, Hamano Shin-Ichiro, Osaka Hitoshi, Hayasaka Kiyoshi, Kinoshita Taroh, Matsumoto Naomic
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