Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Syndrome and GCA[original query] |
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| Endothelial nitric oxide synthase gene polymorphisms in giant cell arteritis. Arthritis and rheumatism 2003 Nov 48 (11): 3219-23. Salvarani Carlo, Casali Bruno, Nicoli Davide, Farnetti Enrico, Macchioni Pierluigi, Catanoso Maria Grazia, Chen Qingquan, Bajocchi GianLuigi, Boiardi Lui |
| Interleukin-6 promoter polymorphism at position -174 in giant cell arteritis. The Journal of rheumatology 2005 Nov 32 (11): 2173-7. Salvarani Carlo, Casali Bruno, Farnetti Enrico, Pipitone Nicolò, Nicoli Davide, Macchioni Pierluigi, Cimino Luca, Bajocchi Gianluigi, Catanoso Maria Grazia, Boiardi Lui |
| Interleukin-10 promoter polymorphisms in giant cell arteritis. Arthritis and rheumatism 2006 Dec 54 (12): 4011-7. Boiardi Luigi, Casali Bruno, Farnetti Enrico, Pipitone Nicolò, Nicoli Davide, Macchioni PierLuigi, Cimino Luca, Bajocchi GianLuigi, Catanoso Maria Grazia, Pattacini Laura, Salvarani Car |
| Bcl-2 antagonist killer 1 (BAK1) polymorphisms influence the risk of developing autoimmune rheumatic diseases in women. Annals of the rheumatic diseases 2010 Feb 69 (2): 462-5. Delgado-Vega A M, Castiblanco J, Gómez L M, Diaz-Gallo L-M, Rojas-Villarraga A, Anaya J |
| Association of genetic variants in senataxin and Alzheimer's disease in a Chinese Han population in Taiwan. The Chinese journal of physiology 2014 Apr 57 (2): 83-9. Shen Che-Piao, Lin Wei-Yong, Lin Ting-Fang, Wang Wen-Fu, Tsai Chon-Haw, Hsu Ban-Dar, Huang Chih-Yang, Liu Hsin-Ping, Tsai Fuu-J |
| Prevalence of the rs1801282 single nucleotide polymorphism of the PPARG gene in patients with metabolic syndrome. Archives of endocrinology and metabolism 2015 Aug 59 (4): 297-302. Rocha Renato Marano, Barra Gustavo Barcelos, Rosa Érica Carine Campos Caldas, Garcia Érica Correa, Amato Angélica Amorim, Azevedo Monalisa Ferrei |
| [ROLE OF SLC2A9 AND ABCG2 GENE POLYMORPHISMS IN ORIGIN OF HYPERURICEMIA AND GOUT]. Georgian medical news 2016 Mar (252): 79-83. Fadieieva A, Prystupa L, Pogorelova O, Kirichenko N, Dudchenko |
| Association of rs9939609 Polymorphism with Metabolic Parameters and FTO Risk Haplotype Among Tunisian Metabolic Syndrome. Metabolic syndrome and related disorders 2016 Jan . Elouej Sahar, Belfki-Benali Hanen, Nagara Majdi, Lasram Khaled, Attaoua Redha, Sallem Om Kalthoum, Kamoun Ines, Chargui Mariem, Romdhane Lilia, Jamoussi Henda, Turki Zinet, Abid Abdelmajid, Ben Slama Claude, Bahri Sonia, Abdelhak Sonia, Grigorescu Florin, Ben Romdhane Habiba, Kefi R |
| Molecular & biochemical analysis of Pro12Ala variant of PPAR-?2 gene in type 2 diabetes mellitus. Saudi journal of biological sciences 2020 Sep 27 (9): 2439-2443. Syed Rabbani, Jamil Kaiser, Asimuddin M, Alqahtani Mohammed S, Alshehri Meshal, Mateen Ayesha, Wahab Ali Aduderman Abdul, Shamsul Ola Mohammad, Malik Abd |
| Interleukin-10 promoter polymorphisms and haplotypes in patients with Guillain-Barré syndrome. Annals of clinical and translational neurology 2023 11 . Shoma Hayat, Asaduzzaman Asad, Moriam Akter Munni, Md Abu Jaher Nayeem, Md Golam Mostafa, Israt Jahan, Md Zakir Hossain Howlader, Quazi Deen Mohammad, Zhahirul Isl |
| [Study of GCN repeats of PHOX2B gene among individuals from southwest China and diagnosis of two patients with Congenital central hypoventilation syndrome]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2024 1 41 (1): 32-37. Shengfang Qin, Mengling Ye, Yan Yin, Jin Wang, Xueyan Wang, Zhuo Zhang, Ximin Chen, Mengjia Yan, Yuxia He, Danying Yi, Qin De |
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