Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Abnormalities and HFE[original query] |
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| HFE mutations and transferrin receptor polymorphism analysis in porphyria cutanea tarda: a prospective study of 36 cases from southern France. The British journal of dermatology 2001 Mar 144 (3): 533-9. Dereure O, Aguilar-Martinez P, Bessis D, Perney P, Vallat C, Guillot B, Blanc F, Guilhou J |
| Clinical expression and insulin sensitivity in type 2 diabetic patients with heterozygous mutations for haemochromatosis. Diabetes & metabolism 2002 Feb 28 (1): 33-8. Van Lerberghe S, Hermans M P, Dahan K, Buysschaert |
| Hemochromatosis (HFE) gene sequence analysis of formalin-fixed, paraffin-embedded liver biopsy specimens. Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology 2001 Dec 6 (4): 227-32. Przygodzki R M, Goodman Z D, Rabin L, Centeno J A, Liu Y, Hubbs A E, O'Leary T |
| 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 |
| Clinical relevance of hemochromatosis-related HFE C282Y/H63D gene mutations in patients on chronic dialysis. Clinical nephrology 2002 Dec 58 (6): 438-44. Canavese C, Bergamo D, Barbieri S, Timbaldi M, Thea A, Martina G, Damiani D, Fenoglio R, Donati-Marella B, Priolo |
| Liver iron deposits in hepatitis B patients: association with severity of liver disease but not with hemochromatosis gene mutations. Journal of gastroenterology and hepatology 2004 Sep 19 (9): 1036-41. Martinelli Ana L C, Filho Antonio B Araujo, Franco Rendrik F, Tavella Marli H, Ramalho Leandra N Z, Zucoloto Sergio, Rodrigues Sandra S, Zago Marcos |
| Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience. Haematologica 2004 Oct 89 (10): 1161-7. De Gobbi Marco, D'Antico Sergio, Castagno Franco, Testa Domenico, Merlini Roberta, Bondi Alessandro, Camaschella Cla |
| Association between heterozygosity for HFE gene mutations and hepatitis viruses in hepatocellular carcinoma. Blood cells, molecules & diseases 0 35 (1): 27-32. Fracanzani Anna Ludovica, Fargion Silvia, Stazi Maria Antonietta, Valenti Luca, Amoroso Pietro, Cariani Elisabetta, Sangiovanni Angelo, Tommasini Maurizio, Rossini Angelo, Bertelli Cristina, Fatta Erika, Patriarca Valeria, Brescianini Sonia, Stroffolini Toma |
| [Hereditary hemochromatosis: phenotypic study in a Spanish population]. Medicina clínica 2005 Nov 125 (19): 721-6. Vázquez-Romero Manuel, Boixeda-de Miquel Daniel, Vallcorba-Gómez del Valle Isabel, Foruny-Olcina José Ramón, Martín de Argila Carlos, San Román-Cos-Gayón Carl |
| Nonalcoholic steatohepatitis in Asian Indians is neither associated with iron overload nor with HFE gene mutations. World journal of gastroenterology : WJG 2005 Jan 11 (3): 393-5. Duseja Ajay, Das Reena, Nanda Mohit, Das Ashim, Garewal Gurjeewan, Chawla Yoge |
| HFE genotypes in decompensated alcoholic liver disease: phenotypic expression and comparison with heavy drinking and with normal controls. The American journal of gastroenterology 2006 Feb 101 (2): 304-10. Gleeson Dermot, Evans Steven, Bradley Martin, Jones Jayne, Peck Robert J, Dube Asha, Rigby Emma, Dalton A |
| Elevated MCP-1 serum levels are associated with the H63D mutation and not the C282Y mutation in hereditary hemochromatosis. Tissue antigens 2007 Oct 70 (4): 294-300. Lawless M W, White M, Mankan A K, O'Dwyer M J, Norris |
| Determinants and characteristics of mean corpuscular volume and hemoglobin concentration in white HFE C282Y homozygotes in the hemochromatosis and iron overload screening study. American journal of hematology 2007 Oct 82 (10): 898-905. McLaren Christine E, Barton James C, Gordeuk Victor R, Wu Lu, Adams Paul C, Reboussin David M, Speechley Mark, Chang Henry, Acton Ronald T, Harris Emily L, Ruggiero Andrea M, Castro Oswaldo, |
| HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening. Genetic testing 2007 11 (3): 269-75. Barton James C, Acton Ronald T, Leiendecker-Foster Catherine, Lovato Laura, Adams Paul C, McLaren Gordon D, Eckfeldt John H, McLaren Christine E, Reboussin David M, Gordeuk Victor R, Speechley Mark R, Reiss Jacob A, Press Richard D, Dawkins Fitzroy W, |
| Highly sensitivity adhesion molecules detection in hereditary haemochromatosis patients reveals altered expression. International journal of immunogenetics 2010 Apr 37 (2): 125-33. Norris S, White M, Mankan A K, Lawless M |
| The C282Y polymorphism of the hereditary hemochromatosis gene is associated with increased sex hormone-binding globulin and normal testosterone levels in men. Journal of endocrinological investigation 2010 Sep 33 (8): 544-8. Yeap B B, Beilin J, Shi Z, Knuiman M W, Olynyk J K, Chubb S A P, Bruce D G, Milward E |
| Early interplay of intra-hepatic iron and insulin resistance in children with non-alcoholic fatty liver disease. Journal of hepatology 2011 Sep 55 (3): 647-53. Manco Melania, Alisi Anna, Fernandez Real Jose-Manuel, Equitani Francesco, Devito Rita, Valenti Luca, Nobili Valer |
| Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease. Neurobiology of aging 2012 Aug 33 (8): 1633-41. Giambattistelli Federica, Bucossi Serena, Salustri Carlo, Panetta Valentina, Mariani Stefania, Siotto Mariacristina, Ventriglia Mariacarla, Vernieri Fabrizio, Dell'acqua Maria Luisa, Cassetta Emanuele, Rossini Paolo Maria, Squitti Rosan |
| Phenotypic and clinical manifestations of compound heterozygous genetic haemochromatosis (CHGH): a non-invasive approach to clinical management. Internal medicine journal 2013 Mar 43 (3): 254-61. Ramakrishna R, Gupta S, Sarathy K, Bowen |
| Iron overload is rare in patients homozygous for the H63D mutation. Canadian journal of gastroenterology & hepatology 2014 Apr 28 (4): 198-202. Kelley Melissa, Joshi Nikhil, Xie Yagang, Borgaonkar Ma |
| HFE genotyping in patients with elevated serum iron indices and liver diseases. BioMed research international 2015 2015 164671. Evangelista Andreia Silva, Nakhle Maria Cristina, de Araújo Thiago Ferreira, Abrantes-Lemos Clarice Pires, Deguti Marta Mitiko, Carrilho Flair José, Cançado Eduardo Luiz Rach |
| Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study. Medicine 2015 Jan 94 (4): e464. Määttä Kirsi M, Nikkari Seppo T, Kunnas Tarja |
| Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension: The TAMRISK study. Medicine 2017 Feb 96 (5): e6052. Nikkari Seppo T, Visto Anni-Laura, Määttä Kirsi M, Kunnas Tarja |
| Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene. Journal of pediatric hematology/oncology 2021 2 44 (1): e68-e73. Kaczorowska-Hac Barbara, Luszczyk Marcin, Wasilewska Eliza, Antosiewicz Jedrzej, Kaczor Jan |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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