Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Syndrome and SAA[original query] |
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Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome. Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis 2005 Jun 12 (2): 115-9. van der Hilst J C H, Drenth J P H, Bodar E J, Bijzet J, van der Meer J W M, Simon A, |
Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.
PLoS genetics 2010 Nov 6 (11): e1001213. Marzi Carola, Albrecht Eva, Hysi Pirro G, Lagou Vasiliki, Waldenberger Melanie, Tönjes Anke, Prokopenko Inga, Heim Katharina, Blackburn Hannah, Ried Janina S, Kleber Marcus E, Mangino Massimo, Thorand Barbara, Peters Annette, Hammond Christopher J, Grallert Harald, Boehm Bernhard O, Kovacs Peter, Geistlinger Ludwig, Prokisch Holger, Winkelmann Bernhard R, Spector Tim D, Wichmann H-Erich, Stumvoll Michael, Soranzo Nicole, März Winfried, Koenig Wolfgang, Illig Thomas, Gieger Christi |
Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature. Arthritis research & therapy 2013 15 (1): R30. Rowczenio Dorota M, Trojer Hadija, Russell Tonia, Baginska Anna, Lane Thirusha, Stewart Nicola M, Gillmore Julian D, Hawkins Philip N, Woo Patricia, Mikoluc Bozena, Lachmann Helen |
SAA1 gene variants and childhood obesity in China. Lipids in health and disease 2013 12 (1): 161. Zhang Xiao, Tang Qi-Zhu, Wan Ai-Ying, Zhang Hai-Ju, Wei |
Controlled exposure of humans with metabolic syndrome to concentrated ultrafine ambient particulate matter causes cardiovascular effects. Toxicological sciences : an official journal of the Society of Toxicology 2014 Jul 140 (1): 61-72. Devlin Robert B, Smith Candice B, Schmitt Michael T, Rappold Ana G, Hinderliter Alan, Graff Don, Carraway Martha S |
Serum amyloid A1 (SAA1) gene polymorphisms in Japanese patients with adult-onset Still's disease. Medicine 2018 Dec 97 (49): e13394. Yashiro Makiko, Furukawa Hiroshi, Asano Tomoyuki, Sato Shuzo, Kobayashi Hiroko, Watanabe Hiroshi, Suzuki Eiji, Nakamura Tadashi, Koga Tomohiro, Shimizu Toshimasa, Umeda Masataka, Nonaka Fumiaki, Ueki Yukitaka, Eguchi Katsumi, Kawakami Atsushi, Migita Kiyos |
Challenges in the interpretation of a germline TERT variant in a patient with juvenile myelomonocytic leukemia. Pediatric blood & cancer 2022 8 69 (10): e29909. Janczar Szymon, Kirschner Martin, Beier Fabian, Brümmendorf Tim H, Ussowicz Marek, Babol-Pokora Katarzyna, Oszer Aleksandra, Yoshimi Ayami, Kalwak Krzysztof, Mlynarski Wojcie |
Genetic testing in severe aplastic anemia is required for optimal hematopoietic cell transplant outcomes. Blood 2022 Jul . McReynolds Lisa J, Rafati Maryam, Wang Youjin, Ballew Bari J, Kim Jung, Williams Valencia V, Zhou Weiyin, Hendricks Rachel M, Dagnall Casey, Freedman Neal D, Carter Brian, Strollo Sara, Hicks Belynda, Zhu Bin, Jones Kristine, Paczesny Sophie, Marsh Steven G E, Spellman Stephen R, He Meilun, Wang Tao, Lee Stephanie J, Savage Sharon A, Gadalla Shahinaz |
Lymphocyte Activation Gene 3 Single-Nucleotide Polymorphisms in Bone Marrow Failure Diseases. Analytical cellular pathology (Amsterdam) 2022 3 2022 3528598. Sun Yingying, Cao Qiuying, Zhao Xiaoyu, Liu Chunyan, Shao Zongho |
Optical coherence tomography assessment of disease activity in cryopyrin-associated periodic syndrome. European journal of neurology 2024 4 e16301. E Mulazzani, L Böhm, T Christmann, M Krumbholz, T Kümpfel, J Hav |
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- Page last updated:May 06, 2024
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