Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and C3[original query] |
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STAT4 gene polymorphism in two major autoimmune diseases (multiple sclerosis and juvenile onset systemic lupus erythematosus) and its relation to disease severity. The Egyptian journal of neurology, psychiatry and neurosurgery 2018 54 (1): 16. Nageeb Rania S, Omran Alaa A, Nageeb Ghada S, Yousef Manal A, Mohammad Yassir A A, Fawzy Am |
Convergent effects of a functional C3 variant on brain atrophy, demyelination, and cognitive impairment in multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2018 2 25 (4): 532-540. Roostaei Tina, Sadaghiani Shokufeh, Mashhadi Rahil, Falahatian Masih, Mohamadi Esmaeil, Javadian Nina, Nazeri Aria, Doosti Rozita, Naser Moghadasi Abdorreza, Owji Mahsa, Hashemi Taheri Amir Pejman, Shakouri Rad Ali, Azimi Amirreza, Voineskos Aristotle N, Nazeri Arash, Sahraian Mohammad A |
Early complement genes are associated with visual system degeneration in multiple sclerosis.
Brain : a journal of neurology 2019 Sep 142 (9): 2722-2736. Fitzgerald Kathryn C, Kim Kicheol, Smith Matthew D, Aston Sean A, Fioravante Nicholas, Rothman Alissa M, Krieger Stephen, Cofield Stacey S, Kimbrough Dorlan J, Bhargava Pavan, Saidha Shiv, Whartenby Katharine A, Green Ari J, Mowry Ellen M, Cutter Gary R, Lublin Fred D, Baranzini Sergio E, De Jager Philip L, Calabresi Peter |
Role of lectin pathway complement proteins and genetic variants in organ damage and disease severity of systemic sclerosis: a cross-sectional study. Arthritis research & therapy 2019 Mar 21 (1): 76. Osthoff Michael, Jaeger Veronika K, Heijnen Ingmar A F M, Trendelenburg Marten, Jordan Suzana, Distler Oliver, Walker Ulrich |
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