Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Leukoaraiosis and MTHFR[original query] |
---|
Evaluation of the roles of common genetic mutations in leukoaraiosis. Acta neurologica Scandinavica 2001 Nov 104 (5): 281-7. Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Fodor |
Specific APO E genotypes in combination with the ACE D/D or MTHFR 677TT mutation yield an independent genetic risk of leukoaraiosis. Acta neurologica Scandinavica 2004 Mar 109 (3): 222-7. Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Fodor L, Bene J, Melegh |
Evaluation of the MTHFR A1298C variant in leukoaraiosis. Journal of molecular neuroscience : MN 2012 Mar 46 (3): 492-6. Szolnoki Zoltan, Szaniszlo Istvan, Szekeres Marta, Hitri Krisztina, Kondacs Andras, Mandi Yvette, Nedo Erika, Somogyvari Fere |
Analysis of genetic polymorphisms associated with leukoaraiosis in the southern Chinese population: A case-control study. Medicine 2016 Aug 95 (35): e3857. Huang Wen-Qing, Ye Hui-Ming, Li Fang-Fang, Yi Ke-Hui, Zhang Ya, Cai Liang-Liang, Lin Hui-Nuan, Lin Qing, Tzeng Chi-Me |
Homocysteinemia is Associated with the Presence of Microbleeds in Cognitively Impaired Patients. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2020 9 29 (12): 105302. Yoo Jun Sang, Ryu Chang-Hwan, Kim Young Seo, Kim Hee-Jin, Bushnell Cheryl D, Kim Hyun You |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
- Content source: