10.1016/s0168-8278(00)80415-8
Crossref journal-article
Elsevier BV
Journal of Hepatology (78)
Bibliography

Powell, L. W., Nathan Subramaniam, V., & Yapp, T. R. (2000). Haemochromatosis in the new millenium. Journal of Hepatology, 32, 48–62.

Authors 3
  1. Lawrie W. Powell (first)
  2. V. Nathan Subramaniam (additional)
  3. Thomas R. Yapp (additional)
References 116 Referenced 55
  1. {'key': '10.1016/S0168-8278(00)80415-8_BIB1', 'first-page': '663', 'article-title': 'Glycosurie, diabete sucre', 'author': 'Trousseau', 'year': '1865'} / Glycosurie, diabete sucre by Trousseau (1865)
  2. {'first-page': '324', 'year': '1889', 'author': 'von Recklinghausen', 'key': '10.1016/S0168-8278(00)80415-8_BIB2'} by von Recklinghausen (1889)
  3. {'first-page': '382', 'year': '1935', 'author': 'Sheldon', 'key': '10.1016/S0168-8278(00)80415-8_BIB3'} by Sheldon (1935)
  4. 10.1002/hep.1840060106 / Hepatology / Value of hepatic iron measurements in early hemochromatosis and determination of the critical iron level associated with fibrosis by Bassett (1986)
  5. 10.1002/path.1700840107 / J Pathol Bacteriol / Hepatic pathology in relatives of patients with haemochromatosis by Scheuer (1962)
  6. 10.1053/gast.1997.v112.pm9041250 / Gastroenterology / Hemosiderosis in cirrhosis: A study of 447 native livers by Ludwig (1997)
  7. 10.1016/S0168-8278(98)80011-1 / J Hepatol / End-stage liver disease without hemochromatosis associated with elevated hepatic iron index by Cotler (1998)
  8. 10.1038/ng0896-399 / Nat Genet / A novel MHC class-I like gene is mutated in patients with hereditary haemochromatosis by Feder (1996)
  9. {'key': '10.1016/S0168-8278(00)80415-8_BIB9', 'series-title': "Schiff's Diseases of the Liver", 'article-title': 'Hemochromatosis and other iron storage disorders', 'author': 'Powell', 'year': '1998'} / Schiff's Diseases of the Liver / Hemochromatosis and other iron storage disorders by Powell (1998)
  10. {'key': '10.1016/S0168-8278(00)80415-8_BIB10', 'first-page': '385', 'article-title': 'Hereditary haemochromatosis in Denmark 1950–1985: clinical, biochemical and histological features in 179 patients and 13 preclinical cases', 'volume': '38', 'author': 'Milman', 'year': '1991', 'journal-title': 'Dan Med Bull'} / Dan Med Bull / Hereditary haemochromatosis in Denmark 1950–1985: clinical, biochemical and histological features in 179 patients and 13 preclinical cases by Milman (1991)
  11. 10.1002/hep.510250130 / Hepatology / The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis by Adams (1997)
  12. 10.1056/NEJM199909023411002 / N Engl J Med / A population based study of the clinical expression of the hemochromatosis gene by Olynyk (1999)
  13. 10.1016/S0016-5085(79)80146-8 / Gastroenterology / Idiopathic hemochromatosis in a young female. A case study and review of the syndrome in young people by Lamon (1979)
  14. 10.7326/0003-4819-67-1-117 / Ann Intern Med / Hemochromatosis in two young sisters. Case studies and a family survey by Felts (1967)
  15. {'key': '10.1016/S0168-8278(00)80415-8_BIB15', 'first-page': '132', 'article-title': 'Idiopathic hemochromatosis in young subjects. Clinical, pathological, and chemical findings in four patients', 'volume': '83', 'author': 'Charlton', 'year': '1967', 'journal-title': 'Arch Pathol'} / Arch Pathol / Idiopathic hemochromatosis in young subjects. Clinical, pathological, and chemical findings in four patients by Charlton (1967)
  16. 10.1007/BF00286653 / Hum Genet / Juvenile idiopathic haemochromatosis: a life-threatening disorder presenting as hypogonadotropic hypogonadism by Cazzola (1983)
  17. 10.1159/000484794 / Eur J Hum Genet / Juvenile and adult hemochromatosis are distinct genetic disorders by Camaschella (1997)
  18. 10.1086/302379 / Am J Hum Genet / Juvenile hemochromatosis locus maps to chromosome 1q by Roetto (1999)
  19. {'key': '10.1016/S0168-8278(00)80415-8_BIB19', 'first-page': '75', 'article-title': 'Neonatal hemochromatosis', 'volume': '23', 'author': 'Knisely', 'year': '1987', 'journal-title': 'Birth Defects'} / Birth Defects / Neonatal hemochromatosis by Knisely (1987)
  20. 10.1016/0046-8177(89)90042-7 / Hum Pathol / Perinatal hemochromatosis: entity or end result? by Witzelbin (1989)
  21. {'key': '10.1016/S0168-8278(00)80415-8_BIB21', 'first-page': '538', 'article-title': 'Perinatal hemochromatosis: clinical morphologic and quantitative iron studies', 'volume': '128', 'author': 'Silver', 'year': '1987', 'journal-title': 'Am J Pathol'} / Am J Pathol / Perinatal hemochromatosis: clinical morphologic and quantitative iron studies by Silver (1987)
  22. 10.1136/jmg.33.6.444 / J Med Genet / Recurrence of neonatal haemochromatosis in half sibs born of unaffected mothers by Verloes (1996)
  23. 10.1097/00005176-199210000-00017 / J Pediatr Gastroenterol Nutr / Neonatal hemochromatosis: report of successful orthotopic liver transplantation by Rand (1992)
  24. 10.1016/S0065-3101(24)00290-1 / Adv Pediatrics / Neonatal hemochromatosis by Knisely (1992)
  25. {'year': '1964', 'author': 'MacDonald', 'key': '10.1016/S0168-8278(00)80415-8_BIB25'} by MacDonald (1964)
  26. 10.1136/gut.17.5.332 / Gut / Association of HLA A3 and HLA B14 antigens with idiopathic hemochromatosis by Simon (1976)
  27. 10.1136/bmj.4.5995.520-b / Br Med J / HLA antigens in haemochromatosis by Walters (1975)
  28. 10.1111/j.1399-0004.1977.tb01324.x / Clin Genet / Heredity of idiopathic hemochromatosis: a study of 106 families by Simon (1977)
  29. 10.1016/0198-8859(81)90011-2 / Human Immunol / Idiopathic hemochromatosis in the Australian population: HLA linkage and recessivity by Doran (1981)
  30. 10.1007/BF00293874 / Hum Genet / HLA as a marker of the hemochromatosis gene in Sweden by Ritter (1984)
  31. {'key': '10.1016/S0168-8278(00)80415-8_BIB31', 'first-page': '41', 'article-title': 'HLA determinants in an Australian population of hemochromatosis patients and their families', 'volume': '45', 'author': 'Summers', 'year': '1989', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / HLA determinants in an Australian population of hemochromatosis patients and their families by Summers (1989)
  32. 10.1084/jem.184.5.1975 / J Exp Med / Defective iron homeostasis in Beta2-microglobulin knockout mice recapitulates hereditary hemochromatosis in man by Santos (1996)
  33. 10.1073/pnas.93.4.1529 / Proc Natl Acad Sci USA / Beta-2-microglobulin knockout mice develop parenchymal iron overload: a putative role for class I genes of the major histocompatibility complex in iron metabolism by Rothenberg (1996)
  34. {'key': '10.1016/S0168-8278(00)80415-8_BIB34', 'first-page': '828', 'article-title': 'Mutation analysis of the HLA-H gene in Italian hemochromatosis patients', 'volume': '60', 'author': 'Carella', 'year': '1997', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Mutation analysis of the HLA-H gene in Italian hemochromatosis patients by Carella (1997)
  35. 10.1038/ng1196-249 / Nat Genet / Haemochromatosis and HLA-H [letter] by Jazwinska (1996)
  36. 10.1038/ng1196-251 / Nat Genet / Haemochromatosis and HLA-H by Jouanolle (1996)
  37. 10.1136/gut.41.6.841 / Gut / A simple genetic test identifies 90% of UK patients with haemochromatosis by Worwood (1997)
  38. 10.1016/S0016-5085(99)70244-1 / Gastroenterology / Molecular medicine and hemochromatosis: at the crossroads by Bacon (1999)
  39. 10.1056/NEJM199909023411003 / N Engl J Med / Hereditary hemochromatosis in adults without pathogenic mutations in the hemochromatosis gene by Pietrangelo (1999)
  40. 10.1016/S0016-5085(99)70505-6 / Gastoenterology / A novel mutation of HFE explains the classical phenotype of genetic hemochromatosis in a C282Y heterozygote by Wallace (1999)
  41. 10.1182/blood.V93.8.2502 / Blood / HFE mutations analysis in 711 hemochromatosis probands: evidence for S65C implication in mild form of hemochromatosis by Mura (1999)
  42. 10.1056/NEJM198805263182103 / N Engl J Med / Prevalence of hemochromatosis among 11,065 presumably healthy blood donors by Edwards (1988)
  43. 10.1111/j.1365-2141.1990.tb06345.x / Br J Haematol / Prevalence of haemochromatosis amongst asymptomatic Australians by Leggett (1990)
  44. 10.1136/jmg.34.4.275 / J Med Genet / Global prevalence of putative haemochromatosis mutations by Merryweather-Clarke (1997)
  45. 10.1182/blood.V90.10.4236 / Blood / Neonatal screening for the haemochromatosis defect by Cullen (1997)
  46. 10.1086/302318 / Am J Hum Genet / Multicentric origin of HFE mutations by Rochette (1999)
  47. 10.1016/S0140-6736(96)09436-6 / Lancet / Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda by Roberts (1997)
  48. 10.1002/hep.510270128 / Hepatology / High prevalence of the His63Asp HFE mutation in Italian patients with porphyria curtanea tarda by Sampietro (1998)
  49. 10.1016/S0168-8278(98)80313-9 / J Hepatol / The C282Y mutation in haemochromatosis (HFE) gene and hepatitis C virus infection are independent cofactors for porphyria cutanea tarda in Australian patients by Stuart (1998)
  50. 10.1093/hmg/8.8.1517 / Hum Mol Genet / Spectrum of mutations in the HFE gene implication in haemochromatosis and porphyria by Villiers (1999)
  51. 10.1016/S0016-5085(98)70482-2 / Gastroenterology / Increased hepatic iron stores on non alcoholic steatohepatitis are associated with the hemochromatosis mutation and increased liver damage by George (1998)
  52. {'key': '10.1016/S0168-8278(00)80415-8_BIB52', 'first-page': '446', 'article-title': 'Increased liver iron stores in patients with hepatocellular carcinoma developed on a noncirrhotic liver', 'volume': '22', 'author': 'Turlin', 'year': '1995', 'journal-title': 'Hepatology'} / Hepatology / Increased liver iron stores in patients with hepatocellular carcinoma developed on a noncirrhotic liver by Turlin (1995)
  53. 10.1002/hep.1840180613 / Hepatology / Preneoplastic significance of hepatic iron-free foci in genetic hemochromatosis: a study of 185 patients by Deugnier (1993)
  54. 10.1016/S0140-6736(81)92463-6 / Lancet / Iron and the sex difference in heart disease risk by Sullivan (1981)
  55. 10.1016/0306-9877(91)90030-3 / Med Hypotheses / Iron stores and the international variation in mortality from coronary artery disease by Lauffer (1990)
  56. 10.1002/hep.510270631 / Hepatology / Heterozygosity for hereditary hemochromatosis is associated with more fibrosis in chronic hepatitis C by Smith (1998)
  57. 10.1006/bcmd.1996.0100 / Blood Cells Molecules Dis / Hemochromatosis: association of severity of iron overload with genetic markers by Barton (1996)
  58. {'key': '10.1016/S0168-8278(00)80415-8_BIB58', 'first-page': '833', 'article-title': 'Concordance of iron storage in siblings with genetic hemochromatosis: evidence for a predominantly genetic effect on iron storage', 'volume': '17', 'author': 'Crawford', 'year': '1993', 'journal-title': 'Hepatology'} / Hepatology / Concordance of iron storage in siblings with genetic hemochromatosis: evidence for a predominantly genetic effect on iron storage by Crawford (1993)
  59. 10.1016/0002-9343(84)90991-4 / Am J Med / Evidence for heterogeneity in hereditary hemochromatosis. Evaluation of 174 persons in nine families by Muir (1984)
  60. 10.1002/ajh.2830450210 / Am J Hematol / Prevalence of abnormal iron studies in heterozygotes for hereditary hemochromatosis: an analysis of 255 heterozygotes by Adams (1994)
  61. 10.1056/NEJM199612123352403 / N Engl J Med / Clinical and biochemical abnormalities in people heterozygous for hemochromatosis by Bulaj (1996)
  62. 10.1007/s002510050211 / Immunogenetics / Mutations in the MHC class I-like candidate gene for hemochromatosis in French patients by Borot (1997)
  63. 10.1006/bcmd.1997.0148 / Blood Cells Molecules Dis / Correlation between genotype and phenotype in hereditary hemochromatosis: analysis of 61 cases by Sham (1997)
  64. {'key': '10.1016/S0168-8278(00)80415-8_BIB64', 'first-page': '362', 'article-title': 'Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene', 'volume': '57', 'author': 'Crawford', 'year': '1995', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Evidence that the ancestral haplotype in Australian hemochromatosis patients may be associated with a common mutation in the gene by Crawford (1995)
  65. 10.1016/S0016-5085(98)70320-8 / Gastroenterology / Expression of HLA-linked hemochromatosis in subjects homozygous or heterozygous subjects for the C282Y mutation by Crawford (1998)
  66. 10.1073/pnas.94.6.2534 / Proc Natl Acad Sci USA / Immunohistochemistry of HLA-H, the protein defective in patients with hereditary hemochromatosis, reveals unique pattern of expression in gastroentestinal tract by Parkkila (1997)
  67. 10.1016/S0378-1119(98)00519-8 / Gene / Cloning, sequencing and characterisation of the rat hereditary hemochromatosis promoter: comparison of the human, mouse and rat HFE promoter regions by Sanchez (1998)
  68. 10.1016/S0140-6736(78)90420-8 / Lancet / Uptake of iron by duodenal biopsy specimens from patients with iron deficiency anaemia and primary haemochromatosis by Cox (1978)
  69. 10.1136/gut.38.5.765 / Gut / A duodenal mucosal abnormality in the reduction of Fe(III) in patients with genetic haemochromatosis by Raja (1996)
  70. 10.1136/gut.11.9.727 / Gut / Intestinal mucosal uptake of iron and iron retention in idiopathic hemochromatosis as evidence of a mucosal abnormality by Powell (1970)
  71. 10.1073/pnas.95.4.1472 / Proc Natl Acad Sci USA / The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding by Feder (1998)
  72. 10.1074/jbc.274.13.9022 / J Biol Chem / The hereditary hemochromatosis protein, HFE, specifically regulates transferrin-mediated iron uptake in HeLa cells by Roy (1999)
  73. 10.1073/pnas.96.4.1579 / Proc Natl Acad Sci USA / Association of HFE protein with transferrin receptor in crypt enterocytes of human duodenum by Waheed (1999)
  74. 10.1074/jbc.273.34.22068 / J Biol Chem / Co-trafficking of HFE, a nonclassical major histocompatibility complex class I protein with the transferrin receptor implies a role in intracellular iron regulation by Gross (1998)
  75. 10.1073/pnas.96.10.5434 / Proc Nat Acad Sci USA / Transferrin receptor is negatively modulated by the hemochromatosis protein HFE: implications for cellular iron homeostasis by Salter-Cid (1999)
  76. 10.1006/jmbi.1999.2842 / J Mol Biol / The transferrin receptor binding site on HFE, the class I MHC-related protein mutated in hereditary hemochromatosis by Lebron (1999)
  77. 10.1038/ng0897-383 / Nat Genet / Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene by Fleming (1997)
  78. 10.1038/41343 / Nature / Cloning and characterization of a mammalian proton-coupled metal-ion transporter by Gunshin (1997)
  79. 10.1073/pnas.93.16.8175 / Proc Natl Acad Sci USA / Molecular control of vertebrate iron metabolism: mRNA-based regulatory circuits operated by iron, nitric-oxide, and oxidative stress by Hentze (1996)
  80. 10.1002/hep.1840070507 / Hepatology / Lack of hepatic transferrin receptor expression in hemochromatosis by Sciot (1987)
  81. 10.1002/hep.1840090102 / Hepatology / Regulation of the hepatic transferrin receptor in hereditary hemochromatosis by Lombard (1989)
  82. 10.1016/0016-5085(92)90161-Q / Gastroenterology / Regulation of transferrin, transferrin receptor and ferritin gene expression in the duodenum of normal anemic and siderotic subjects by Pietrangelo (1992)
  83. 10.1038/5979 / Nat Genet / Hephastin, a ceruloplasmin homologue implicated in intestinal iron transportion, is defective in the sla mouse by Vulpe (1999)
  84. 10.1016/0009-3084(87)90066-1 / Chem Phys Lipids / Lipid peroxidation and associated hepatic organelle dysfunction in iron overload by Britton (1987)
  85. {'key': '10.1016/S0168-8278(00)80415-8_BIB85', 'first-page': '281', 'article-title': 'Iron and the liver: genetic hemochromatosis and other hepatic iron overload disorders', 'volume': '9', 'author': 'Tavill', 'year': '1990', 'journal-title': 'Prog Liver Dis'} / Prog Liver Dis / Iron and the liver: genetic hemochromatosis and other hepatic iron overload disorders by Tavill (1990)
  86. 10.1016/0891-5849(94)90041-8 / Free Rad Biol Med / Genetic hemochromatosis and Wilson's Disease: Role for oxidant stress? by Young (1994)
  87. 10.1097/00041433-199412000-00005 / Curr Opin Lipidol / Lipoprotein oxidation: mechanistic aspects, methodological approaches and clinical relevance by Stocker (1994)
  88. 10.1016/S0168-8278(97)80424-2 / J Hepatol / Hepatic stellate cell activation in genetic hemochromatosis: lobular distribution, effect of increasing hepatic iron and response to phlebotomy by Ramm (1997)
  89. {'key': '10.1016/S0168-8278(00)80415-8_BIB89', 'first-page': 'G908', 'article-title': 'TGF-B and collagen-al (I) gene expression are increased in hepatic acinar zone l of rats with iron overload', 'volume': '5', 'author': 'Houglum', 'year': '1994', 'journal-title': 'Am J Physiol'} / Am J Physiol / TGF-B and collagen-al (I) gene expression are increased in hepatic acinar zone l of rats with iron overload by Houglum (1994)
  90. 10.1172/JCI114934 / J Clin Invest / Malondialdehyde and 4-hydroxynoneal protein adducts in plasma and liver of rats with iron overload by Houglum (1990)
  91. 10.1172/JCI119291 / J Clin Invest / Proliferation of hepatic stellate cells is inhibited by phosphorylation of CREB on serine 133 by Houglum (1997)
  92. 10.1002/hep.510260311 / Hepatology / Excess iron induces hepatic transforming growth factor Beta1 in genetic hemochromatosis: role of oxidative stress by Houglum (1997)
  93. 10.1002/hep.510230656 / Hepatology / Alcohol and iron: A radical combination? by Houglum (1996)
  94. 10.1016/S0002-9297(07)64339-0 / Am J Hum Genet / The significance of the 187G (H63D) mutation in hemochromatosis by Beutler (1997)
  95. 10.1038/11892 / Nat Genet / Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis by Jeffrey (1999)
  96. 10.1016/S0140-6736(97)22005-2 / Lancet / Genetic irony beyond haemochromatosis: clinical effect of HLA-H mutations by Beutler (1997)
  97. 10.1006/bcmd.1997.0143 / Blood Cells Molecules Dis / Compound heterozygotes for hemochromatosis gene mutations: may they help to understand the pathophysiology of the disease? by Martinez (1997)
  98. 10.1038/ng1297-375 / Nat Genet / Haemochromatosis, HFE and genetic complexity by Risch (1997)
  99. 10.1016/S0092-8674(00)81151-4 / Cell / Crystal structure of the hemochromatosis protein HFE and characterization of its interaction with transferrin receptor by Lebron (1998)
  100. 10.1073/pnas.94.23.12384 / Proc Natl Acad Sci USA / Hereditary hemochromatosis: Effects of C282Y and H63D mutations on association with Beta2-microglobulin, intracellular processing and cell surface expression of the HFE protein in COS-7 cells by Waheed (1997)
  101. 10.1073/pnas.94.24.13198 / Proc Natl Acad Sci USA / Association of the transferrin receptor in human placenta with HFE, the protein defective in hereditary hemochromatosis by Parkkila (1997)
  102. 10.1016/0016-5085(90)90276-7 / Gastroenterology / Transferrin receptor distribution and regulation in the rat small intestine: Effect of iron stores and erythropoiesis by Anderson (1990)
  103. 10.1016/0016-5085(86)90687-6 / Gastroenterology / Transferrin receptors in the human gastrointestinal tract. Relationship to body iron stores by Banerjee (1986)
  104. 10.1055/s-2008-1041772 / Semin Liver Dis / Genetic hemochromatosis by Bassett (1997)
  105. 10.1016/S0016-5085(98)70265-3 / Gastroenterology / Non-invasive prediction of fibrosis in C282Y homozygous hemochromatosis by Guyader (1998)
  106. 10.1111/j.1399-0004.1998.tb02672.x / Clin Genet / Implications of genotyping of spouses to limit investigation of children in genetic hemochromatosis by Adams (1998)
  107. 10.1016/S0016-5085(98)70538-4 / Gastroenterology / The distribution of transferrin saturation in an asymptomatic Australian population: relevance to the early diagnosis of hemochromatosis by McLaren (1998)
  108. {'key': '10.1016/S0168-8278(00)80415-8_BIB108', 'first-page': '26', 'article-title': 'Principles and practice of screening for disease', 'author': 'Wilson', 'year': '1986', 'journal-title': 'Public Health Papers WHO'} / Public Health Papers WHO / Principles and practice of screening for disease by Wilson (1986)
  109. {'key': '10.1016/S0168-8278(00)80415-8_BIB109', 'first-page': '422A', 'article-title': 'Automated measurement of unsaturated iron binding capacity allows a cost effective, ongoing strategy for screening for haemochromatosis', 'volume': '28', 'author': 'Hickman', 'year': '1998', 'journal-title': 'Hepatology'} / Hepatology / Automated measurement of unsaturated iron binding capacity allows a cost effective, ongoing strategy for screening for haemochromatosis by Hickman (1998)
  110. 10.1111/j.1572-0241.1999.1120_f.x / Am J Gastroenterol / Screening blood donors for hereditary hemochromatosis: decision analysis model comparing genotyping to phenotyping by Adams (1999)
  111. {'key': '10.1016/S0168-8278(00)80415-8_BIB111', 'article-title': 'HFE-associated haemochromatosis in subjects aged 30 years or younger', 'author': 'Yapp', 'year': '1999', 'journal-title': 'Hepatology'} / Hepatology / HFE-associated haemochromatosis in subjects aged 30 years or younger by Yapp (1999)
  112. 10.1053/gast.1996.v110.pm8613000 / Gastroenterology / Long-term survival in patients with hereditary hemochromatosis by Niederau (1996)
  113. 10.1056/NEJM198511143132004 / N Engl J Med / Survival and causes of death in cirrhotic and in noncirrhotic patients with primary hemochromatosis by Niederau (1985)
  114. {'key': '10.1016/S0168-8278(00)80415-8_BIB114', 'first-page': '421A', 'article-title': 'Effectiveness of regular surveillance for hepatocellular carcinoma in haemochromatosis with cirrhosis', 'volume': '28', 'author': 'Dixon', 'year': '1998', 'journal-title': 'Hepatology'} / Hepatology / Effectiveness of regular surveillance for hepatocellular carcinoma in haemochromatosis with cirrhosis by Dixon (1998)
  115. 10.1111/j.1445-5994.1990.tb01024.x / Aust NZ J Med / Familial iron overload with possible autosomal dominant inheritance by Eason (1990)
  116. {'key': '10.1016/S0168-8278(00)80415-8_BIB116', 'article-title': 'HFE associated hereditary haemochromatosis', 'author': 'Eijkelkamp', 'year': '1999', 'journal-title': 'Can J Gastroenterol'} / Can J Gastroenterol / HFE associated hereditary haemochromatosis by Eijkelkamp (1999)
Dates
Type When
Created 22 years, 10 months ago (Oct. 11, 2002, 8:25 a.m.)
Deposited 8 months, 3 weeks ago (Dec. 8, 2024, 9:46 p.m.)
Indexed 2 months ago (June 30, 2025, 12:03 a.m.)
Issued 25 years, 8 months ago (Jan. 1, 2000)
Published 25 years, 8 months ago (Jan. 1, 2000)
Published Print 25 years, 8 months ago (Jan. 1, 2000)
Funders 0

None

@article{Powell_2000, title={Haemochromatosis in the new millenium}, volume={32}, ISSN={0168-8278}, url={http://dx.doi.org/10.1016/s0168-8278(00)80415-8}, DOI={10.1016/s0168-8278(00)80415-8}, journal={Journal of Hepatology}, publisher={Elsevier BV}, author={Powell, Lawrie W. and Nathan Subramaniam, V. and Yapp, Thomas R.}, year={2000}, month=jan, pages={48–62} }