These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
27. [Hemochromatosis--from an underdiagnosed curiosity to a common disease]. Hagve TA; Asberg A; Ulvik R; Borch-Iohnsen B; Thorstensen K Tidsskr Nor Laegeforen; 2009 Apr; 129(9):863-6. PubMed ID: 19415085 [TBL] [Abstract][Full Text] [Related]
28. Screening for hereditary hemochromatosis. Rochette J; Capron D; Capron JP; Julier C Am J Gastroenterol; 2000 May; 95(5):1368-9. PubMed ID: 10811362 [No Abstract] [Full Text] [Related]
29. One expert's opinion. Weinberg ED MLO Med Lab Obs; 2006 Jan; 38(1):6; discussion 6; author reply 6. PubMed ID: 16493902 [No Abstract] [Full Text] [Related]
30. Iron overload in the liver diagnostic and quantification. Alústiza JM; Castiella A; De Juan MD; Emparanza JI; Artetxe J; Uranga M Eur J Radiol; 2007 Mar; 61(3):499-506. PubMed ID: 17166681 [TBL] [Abstract][Full Text] [Related]
31. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification. Robinson G; Narasimhan S; Weatherall M; Beasley R J Gastroenterol Hepatol; 2007 Jun; 22(6):852-4. PubMed ID: 17565641 [TBL] [Abstract][Full Text] [Related]
32. Hemochromatosis 1991. What will increased clinical screening mean for medical directors? Witte DL; Kay BR J Insur Med; 1991; 23(4):281-3. PubMed ID: 10147832 [No Abstract] [Full Text] [Related]
33. [Hemochromatosis: the importance of mutation screening in the family]. ter Braak N; Erdkamp FL; van Deursen CT Ned Tijdschr Geneeskd; 2009 Apr; 153(16):765-7. PubMed ID: 19469149 [No Abstract] [Full Text] [Related]
34. A genetic defect of an iron pump on chromosome 20 is postulated to cause human hemochromatosis. Peuschel KE Med Hypotheses; 1997 Nov; 49(5):417-9. PubMed ID: 9421808 [TBL] [Abstract][Full Text] [Related]
35. [Hereditary hemochromatosis and use of genetic tests]. Foss Haug KB; Kierulf P; Sandset PM; Urdal P; Wisløff F Tidsskr Nor Laegeforen; 1998 May; 118(12):1911. PubMed ID: 9638063 [No Abstract] [Full Text] [Related]