Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: Death and HFE[original query] |
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Haemochromatosis gene mutations in idiopathic dilated cardiomyopathy. Heart (British Cardiac Society) 2000 Nov 84 (5): 541-7. Mahon N G, Coonar A S, Jeffery S, Coccolo F, Akiyu J, Zal B, Houlston R, Levin G E, Baboonian C, McKenna W |
HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology. American journal of epidemiology 2001 Aug 154 (3): 193-206. Hanson EH, Imperatore G, Burke W |
No increase in mortality and morbidity among carriers of the C282Y mutation of the hereditary haemochromatosis gene in the oldest old: the Leiden 85-plus study. European journal of clinical investigation 2002 Oct 32 (10): 750-4. Van Aken M O, De Craen A J M, Gussekloo J, Moghaddam P Hanifi, Vandenbroucke J P, Heijmans B T, Slagboom P E, Westendorp R G |
Genetic polymorphisms associated with thrombophilia and vascular disease in women with unexplained late intrauterine fetal death: a multicenter study. Journal of the Society for Gynecologic Investigation 2004 Jan 11 (1): 42-4. Hefler Lukas, Jirecek Stefan, Heim Kurt, Grimm Christoph, Antensteiner Gisella, Zeillinger Robert, Husslein Peter, Tempfer Cleme |
HFE genotype influences erythropoiesis support requirement in hemodialysis patients: a prospective study. American journal of nephrology 2008 28 (2): 311-6. Valenti Luca, Valenti Giovanni, Como Giovanna, Santorelli Gennaro, Dongiovanni Paola, Rametta Raffaela, Fracanzani Anna Ludovica, Tavazzi Dario, Messa Pier Giorgio, Fargion Silv |
HFE mutations in heart disease. Heart and vessels 2008 Sep 23 (5): 348-55. Dunn Terence, Blankenship Derek, Beal Nicole, Allen Richard, Schechter Eliot, Moore William, Perveen Ghazala, Eichner Ju |
HFE C282Y homozygotes have reduced low-density lipoprotein cholesterol: the Atherosclerosis Risk in Communities (ARIC) Study. Translational research : the journal of laboratory and clinical medicine 2008 Jul 152 (1): 3-10. Pankow James S, Boerwinkle Eric, Adams Paul C, Guallar Eliseo, Leiendecker-Foster Catherine, Rogowski Jason, Eckfeldt John |
Frequency of the hemochromatosis gene (HFE) variants in a Jordanian Arab population and in diabetics from the same region. Disease markers 2009 27 (1): 17-22. Alkhateeb Asem, Uzrail Amal, Bodoor Khald |
HFE, MTHFR, and FGFR4 genes polymorphisms and breast cancer in Brazilian women. Molecular and cellular biochemistry 2011 Nov 357 (1-2): 247-53. Batschauer Anna P, Cruz Nathalia G, Oliveira Vanessa C, Coelho Fernanda F, Santos Izabela R, Alves Michelle T, Fernandes Ana P, Carvalho Maria G, Gomes Karina |
Correlation of hemochromatosis gene mutations and cardiovascular disease in hemodialysis patients. Annals of Saudi medicine 0 33 (3): 223-8. Bi Min, Li Bing, Li Qia |
Total and cause-specific mortality by elevated transferrin saturation and hemochromatosis genotype in individuals with diabetes: two general population studies. Diabetes care 2014 Feb 37 (2): 444-52. Ellervik Christina, Mandrup-Poulsen Thomas, Tybjærg-Hansen Anne, Nordestgaard Børge |
Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin. Neurobiology of disease 2014 Feb 62 172-8. Rhodes Shannon L, Buchanan Daniel D, Ahmed Ismaïl, Taylor Kent D, Loriot Marie-Anne, Sinsheimer Janet S, Bronstein Jeff M, Elbaz Alexis, Mellick George D, Rotter Jerome I, Ritz Bea |
[Molecular genetic analysis and clinical aspects of patients with hereditary hemochromatosis]. Der Orthopäde 2014 Aug 43 (8): 772-9. Lange U, Teichmann J, Dischereit |
Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. Hereditas 2017 12 154 16. Olsson K Sigvard, Wålinder Olof, Jansson Ulf, Wilbe Maria, Bondeson Marie-Louise, Stattin Eva-Lena, Raha-Chowdhury Ruma, Williams Rog |
Hemochromatosis: Hereditary hemochromatosis and HFE gene. Vitamins and hormones 2019 2 110 201-222. Katsarou Martha-Spyridoula, Papasavva Maria, Latsi Rozana, Drakoulis Nikola |
The Nrf2-mediated defense mechanism associated with HFE genotype limits vulnerability to oxidative stress-induced toxicity. Toxicology 2020 6 441 152525. Song Insung Y, Snyder Amanda M, Kim Yunsung, Neely Elizabeth B, Wade Quinn W, Connor James |
Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy. JAMA 2020 11 324 (20): 2048-2057. Atkins Janice L, Pilling Luke C, Masoli Jane A H, Kuo Chia-Ling, Shearman Jeremy D, Adams Paul C, Melzer Dav |
Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes. Digestive diseases and sciences 2022 7 68 (1): 312-322. Natarajan Yamini, Patel Parth, Chu Jinna, Yu Xian, Hernaez Ruben, El-Serag Hashem, Kanwal Fasi |
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- Page last updated:Apr 22, 2024
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