Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Hemochromatosis and HLA-B[original query] |
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| Unsaturated iron binding capacity and transferrin saturation are equally reliable in detection of HFE hemochromatosis. The American journal of gastroenterology 2002 Aug 97 (8): 2093-9. Murtagh Luke J, Whiley Michael, Wilson Susan, Tran Huy, Bassett Mark |
| The role of hemochromatosis susceptibility gene mutations in protecting against iron deficiency in celiac disease. Gastroenterology 2002 Aug 123 (2): 444-9. Butterworth Jeffrey R, Cooper Brian T, Rosenberg William M C, Purkiss Michael, Jobson Shirley, Hathaway Mark, Briggs David, Howell W Martin, Wood Gordon M, Adams David H, Iqbal Tariq |
| High prevalence of a screening-detected, HFE-unrelated, mild idiopathic iron overload in Northern Italy. Haematologica 2002 May 87 (5): 472-8. Barosi Giovanni, Salvaneschi Laura, Grasso Maurizia, Martinetti Miryam, Marchetti Monia, Bodini Umberto, Reggiani Alessandro, D'Agostino Francesco, Nalli Giulio, Degiuli Alberto, De Silvestri Annalisa, Arbustini Eloi |
| Hemochromatosis gene in leukemia and lymphoma. Leukemia & lymphoma 2002 Mar 43 (3): 467-77. Dorak M Tevfik, Burnett Alan K, Worwood Ma |
| Analysis of HLA-A antigens and C282Y and H63D mutations of the HFE gene in Brazilian patients with hemochromatosis. Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2002 Mar 35 (3): 329-35. Bittencourt P L, Palácios S A, Couto C A, Cançado E L R, Carrilho F J, Laudanna A A, Kalil J, Gayotto L C C, Goldberg A |
| HLA-A and -B alleles and haplotypes in hemochromatosis probands with HFE C282Y homozygosity in central Alabama. BMC medical genetics 2002 Oct 3 (): 9. Barton James C, Acton Ronald |
| HFE mutations in African-American women with non-insulin-dependent diabetes mellitus. Ethnicity & disease 2001 11 (4): 578-84. Acton R T, Barton J C, Bell D S, Go R C, Roseman J |
| [Genetic epidemiology and HLA survey of primary hemochromatosis among Chinese Miao ethnic]. Zhonghua nei ke za zhi 2002 1 40 (10): 673-6. Fu H, Wu H, Zhu |
| Common variable immunodeficiency and IgG subclass deficiency in central Alabama hemochromatosis probands homozygous for HFE C282Y. Blood cells, molecules & diseases 0 31 (1): 102-11. Barton James C, Bertoli Luigi F, Acton Ronald |
| Association between the HFE mutations and longevity: a study in Sardinian population. Mechanisms of ageing and development 2003 Apr 124 (4): 529-32. Carru Ciriaco, Pes Giovanni Mario, Deiana Luca, Baggio Giovannella, Franceschi Claudio, Lio Domenico, Balistreri Carmela Rita, Candore Giuseppina, Colonna-Romano Giuseppina, Caruso Caloge |
| Prevalence of C282Y mutation in patients with rheumatoid arthritis and spondylarthritis. International journal of tissue reactions 2002 24 (3): 105-9. Rovetta G, Grignolo M C, Buffrini L, Monteforte |
| HFE genotype and parameters of iron metabolism in German first-time blood donors - evidence for an increased transferrin saturation in C282Y heterozygotes. Zeitschrift für Gastroenterologie 2003 Nov 41 (11): 1069-76. Raddatz D, Legler T, Lynen R, Addicks N, Ramadori |
| Frequency of the HFE gene mutations in five Italian populations. Blood cells, molecules & diseases 0 29 (3): 267-73. Candore Giuseppina, Mantovani Vilma, Balistreri Carmela Rita, Lio Domenico, Colonna-Romano Giuseppina, Cerreta Vincenzo, Carru Ciriaco, Deiana Luca, Pes Giovanni, Menardi Giuseppe, Perotti Laura, Miotti Valeria, Bevilacqua Elena, Amoroso Antonio, Caruso Caloge |
| HLA haplotype A*03-B*07 in hemochromatosis probands with HFE C282Y homozygosity: frequency disparity in men and women and lack of association with severity of iron overload. Blood cells, molecules & diseases 0 34 (1): 38-47. Barton James C, Wiener Howard W, Acton Ronald T, Go Rodney C |
| HLA haplotypes associated with hemochromatosis mutations in the Spanish population. BMC medical genetics 2004 Oct 5 (): 25. Pacho Arantza, Mancebo Esther, del Rey Manuel J, Castro Maria J, Oliver Desamparados, García-Berciano Miguel, González Luis, Morales Pab |
| Human leukocyte antigen haplotypes and HFE mutations in Spanish hereditary hemochromatosis and sporadic porphyria cutanea tarda. Journal of gastroenterology and hepatology 2005 Mar 20 (3): 456-62. Gonzalez-Hevilla Mario, de Salamanca Rafael E, Morales Pablo, Martínez-Laso Jorge, Fontanellas Antonio, Castro Maria José, Rojo Ricardo, Moscoso Juan, Zamora Jorge, Serrano-Vela Juan Ignacio, Arnaiz-Villena Anton |
| HFE genotyping demonstrates a significant incidence of hemochromatosis in undifferentiated arthritis. Clinical and experimental rheumatology 0 23 (1): 7-12. Cauza E, Hanusch-Enserer U, Etemad M, Köller M, Kostner K, Georg P, Dunky A, Ferenci |
| Analysis of HFE gene mutations and HLA-A alleles in Brazilian patients with iron overload. São Paulo medical journal = Revista paulista de medicina 2006 Mar 124 (2): 55-60. Cançado Rodolfo Delfini, Guglielmi Aline Cristiane de Oliveira, Vergueiro Carmen Silvia Vieitas, Rolim Ernani Geraldo, Figueiredo Maria Stella, Chiattone Carlos Sérg |
| The HLA-A1-B8 haplotype hitchhiking with the hemochromatosis mutation: does it affect the phenotype? European journal of haematology 2007 Nov 79 (5): 429-34. Olsson K Sigvard, Ritter Bernd, Hansson Norbe |
| High prevalence of HFE gene mutations in hemodialysis patients. Minerva urologica e nefrologica = The Italian journal of urology and nephrology 2008 Jun 60 (2): 81-4. Mennella G, Valverde S, Forzan S, Fezzi M, Munaretto G, Gessoni |
| Longer survival associated with HLA-A*03, B*14 among 212 hemochromatosis probands with HFE C282Y homozygosity and HLA-A and -B typing and haplotyping. European journal of haematology 2010 Nov 85 (5): 439-47. Barton James C, Barton J Clayborn, Acton Ronald |
| Diagnostic utility of HFE variants in Spanish patients: association with HLA alleles and role in susceptibility to acute lymphoblastic leukemia. Gene 2012 Nov . Rodríguez-López R, Donoso M, Fernández-Cavada M, González LM, Margallo A, Corral C, Gallego M, de Cáceres MT, Herrera T, González C, Vagace JM, Gervasini G |
| Diabetes in first-degree family members: a predictor of type 2 diabetes in 159 nonscreening Alabama hemochromatosis probands with HFE C282Y homozygosity. Diabetes care 2014 37 (1): 259-66. Barton James C, Barton J Clayborn, Acton Ronald |
| Association between celiac disease and iron deficiency in Caucasians, but not non-Caucasians. Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2013 Jul 11 (7): 808-14. Murray Joseph A, McLachlan Stela, Adams Paul C, Eckfeldt John H, Garner Chad P, Vulpe Chris D, Gordeuk Victor R, Brantner Tricia, Leiendecker-Foster Catherine, Killeen Anthony A, Acton Ronald T, Barcellos Lisa F, Nickerson Debbie A, Beckman Kenneth B, McLaren Gordon D, McLaren Christine |
| Effects of highly conserved major histocompatibility complex (MHC) extended haplotypes on iron and low CD8+ T lymphocyte phenotypes in HFE C282Y homozygous hemochromatosis patients from three geographically distant areas. PloS one 2013 8 (11): e79990. Costa Mónica, Cruz Eugénia, Barton James C, Thorstensen Ketil, Morais Sandra, da Silva Berta M, Pinto Jorge P, Vieira Cristina P, Vieira Jorge, Acton Ronald T, Porto Gra |
| Ancestral association between HLA and HFE H63D and C282Y gene mutations from northwest Colombia. Genetics and molecular biology 2015 Mar 38 (1): 8-13. Rodriguez Libia M, Giraldo Mabel C, Velasquez Laura I, Alvarez Cristiam M, Garcia Luis F, Jimenez-Del-Rio Marlene, Velez-Pardo Carl |
| Beyond Human Leukocyte Antigen Class I Antigens: Hereditary Hemochromatosis Gene Mutations in Recurrent Aphthous Oral Ulcers and Behçet Disease in the South of Tunisia. Medical principles and practice : international journal of the Kuwait University, Health Science Centre 2017 Sep . ElAoud Sahar, Kamoun Arwa, Mahfoudh Nadia, Charfi Aida, Snoussi Mouna, Hachicha Hend, Jerbi Ameni, Dammak Chifa, Frikha Feten, Hakim Faiza, Gaddour Lilia, Bahloul Zouheir, Makni Hafe |
| Comprehensive analysis of HFE gene in hereditary hemochromatosis and in diseases associated with acquired iron overload. World journal of hepatology 2019 3 11 (2): 186-198. de Campos Wagner Narciso, Massaro Juliana Doblas, Cançado Eduardo Luiz Rachid, Wiezel Cláudia Emília Vieira, Simões Aguinaldo Luiz, Teixeira Andreza Correa, de Souza Fernanda Fernandes, Mendes-Junior Celso Teixeira, Martinelli Ana de Lourdes Candolo, Donadi Eduardo Antôn |
| HLA-A*03, the hemochromatosis ancestral haplotype, and phenotypes of referred hemochromatosis probands with HFE p.C282Y homozygosity. Hereditas 2022 Jun 159 (1): 25. Barton James C, Barton J Clayborn, Acton Ronald |
| The ancestral haplotype markers HLA -A3 and B7 do not influence the likelihood of advanced hepatic fibrosis or cirrhosis in HFE hemochromatosis. Scientific reports 2023 5 13 (1): 7775. John K Olynyk, Richard Grainger, Helen Currie, Louise E Ramm, Grant A Ra |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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