Crawford D, Ramm G, Bridle K, Nicoll A, Delatycki M, Olynyk J
Hepatol Int. 2023; 17(3):522-541.
PMID: 37067673
PMC: 10224841.
DOI: 10.1007/s12072-023-10510-3.
Girelli D, Busti F, Brissot P, Cabantchik I, Muckenthaler M, Porto G
Blood. 2021; 139(20):3018-3029.
PMID: 34601591
PMC: 11022970.
DOI: 10.1182/blood.2021011338.
Guo S, Jiang S, Epperla N, Ma Y, Maadooliat M, Ye Z
Blood. 2019; 133(17):1888-1898.
PMID: 30814063
PMC: 6484389.
DOI: 10.1182/blood-2018-10-879585.
Pericleous M, Kelly C
Frontline Gastroenterol. 2018; 9(2):110-114.
PMID: 29588838
PMC: 5868443.
DOI: 10.1136/flgastro-2017-100872.
Fabian E, Schiller D, Graninger W, Langner C, Frei J, Schoellnast H
Wien Klin Wochenschr. 2016; 128(21-22):846-853.
PMID: 27363994
PMC: 5104785.
DOI: 10.1007/s00508-016-1010-0.
Hereditary hemochromatosis.
Geller S, de Campos F
Autops Case Rep. 2015; 5(1):7-10.
PMID: 26484318
PMC: 4608170.
DOI: 10.4322/acr.2014.043.
EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).
Porto G, Brissot P, Swinkels D, Zoller H, Kamarainen O, Patton S
Eur J Hum Genet. 2015; 24(4):479-95.
PMID: 26153218
PMC: 4929861.
DOI: 10.1038/ejhg.2015.128.
Factors influencing disease phenotype and penetrance in HFE haemochromatosis.
Rochette J, Gac G, Lassoued K, Ferec C, Robson K
Hum Genet. 2010; 128(3):233-48.
PMID: 20607553
DOI: 10.1007/s00439-010-0852-1.
Phenotypic expression of hereditary hemochromatosis: what have we learned from the population studies?.
Gan E, Ayonrinde O, Trinder D, Olynyk J
Curr Gastroenterol Rep. 2010; 12(1):7-12.
PMID: 20425479
DOI: 10.1007/s11894-009-0078-3.
Impact of gene patents and licensing practices on access to genetic testing for hereditary hemochromatosis.
Chandrasekharan S, Pitlick E, Heaney C, Cook-Deegan R
Genet Med. 2010; 12(4 Suppl):S155-70.
PMID: 20393306
PMC: 3131230.
DOI: 10.1097/GIM.0b013e3181d7acb0.
Serum ferritin is a clinical biomarker in Japanese patients with nonalcoholic steatohepatitis (NASH) independent of HFE gene mutation.
Yoneda M, Nozaki Y, Endo H, Mawatari H, Iida H, Fujita K
Dig Dis Sci. 2009; 55(3):808-14.
PMID: 19267193
DOI: 10.1007/s10620-009-0771-y.
Zinc-gene interaction related to inflammatory/immune response in ageing.
Mocchegiani E, Malavolta M
Genes Nutr. 2008; 3(2):61-75.
PMID: 18850188
PMC: 2467449.
DOI: 10.1007/s12263-008-0085-2.
Intracellular iron transport and storage: from molecular mechanisms to health implications.
MacKenzie E, Iwasaki K, Tsuji Y
Antioxid Redox Signal. 2008; 10(6):997-1030.
PMID: 18327971
PMC: 2932529.
DOI: 10.1089/ars.2007.1893.
Normal iron metabolism and the pathophysiology of iron overload disorders.
Siah C, Ombiga J, Adams L, Trinder D, Olynyk J
Clin Biochem Rev. 2006; 27(1):5-16.
PMID: 16886043
PMC: 1390789.
Frequency of common HFE variants in the Saudi population: a high throughput molecular beacon-based study.
Alsmadi O, Al-Kayal F, Al-Hamed M, Meyer B
BMC Med Genet. 2006; 7:43.
PMID: 16672055
PMC: 1468397.
DOI: 10.1186/1471-2350-7-43.
Fatty liver in H63D homozygotes with hyperferritinemia.
Sebastiani G, Wallace D, Davies S, Kulhalli V, Walker A, Dooley J
World J Gastroenterol. 2006; 12(11):1788-92.
PMID: 16586555
PMC: 4124361.
DOI: 10.3748/wjg.v12.i11.1788.
Haemochromatosis protein is expressed on the terminal web of enterocytes in proximal small intestine of the rat.
West A, Thomas C, Sadlier J, Oates P
Histochem Cell Biol. 2005; 125(3):283-92.
PMID: 16208485
DOI: 10.1007/s00418-005-0060-6.
Prevalence of HFE mutations and relation to serum iron status in patients with chronic hepatitis C and patients with nonalcoholic fatty liver disease in Taiwan.
Lin T, Lin C, Wang C, Liu S, Liao L
World J Gastroenterol. 2005; 11(25):3905-8.
PMID: 15991291
PMC: 4504894.
DOI: 10.3748/wjg.v11.i25.3905.
Recent advances in understanding haemochromatosis: a transition state.
Robson K, Merryweather-Clarke A, Cadet E, Viprakasit V, Zaahl M, Pointon J
J Med Genet. 2004; 41(10):721-30.
PMID: 15466004
PMC: 1735598.
DOI: 10.1136/jmg.2004.020644.
Screening for hemochromatosis in Turkey.
Bozkaya H, Bektas M, Metin O, Erkan O, Ibrahimoglu D, Dalva K
Dig Dis Sci. 2004; 49(3):444-9.
PMID: 15139495
DOI: 10.1023/b:ddas.0000020500.26184.ce.