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.
103 related articles for article (PubMed ID: 13773437)
21. [Hemochromatosis: the clinical picture, diagnosis and treatment]. Kaliuzhnyĭ IT Ter Arkh; 1988; 60(2):121-6. PubMed ID: 3285499 [TBL] [Abstract][Full Text] [Related]
22. [Significance of "minor" genetic mutations in hereditary hemochromatosis: 2 case reports]. Maccari S; Plancher AC Ann Ital Med Int; 2000; 15(3):221-5. PubMed ID: 11059064 [TBL] [Abstract][Full Text] [Related]
23. [Hemochromatosis: various presentations of a changed disease picture]. Salm E; Hart W Ned Tijdschr Geneeskd; 1993 Aug; 137(34):1697-700. PubMed ID: 8371808 [No Abstract] [Full Text] [Related]
24. Role of hemochromatosis genes in chronic hepatitis C. Gattoni A; Parlato A; Vangieri B; Bresciani M; Derna R; Baldassarre R Clin Ter; 2006; 157(1):61-8. PubMed ID: 16669553 [TBL] [Abstract][Full Text] [Related]
25. Hypogonadism and sexual dysfunction in hemochromatosis: the effects of cirrhosis and diabetes. Cundy T; Bomford A; Butler J; Wheeler M; Williams R J Clin Endocrinol Metab; 1989 Jul; 69(1):110-6. PubMed ID: 2732293 [TBL] [Abstract][Full Text] [Related]
26. Molecular aspects of iron absorption: Insights into the role of HFE in hemochromatosis. Philpott CC Hepatology; 2002 May; 35(5):993-1001. PubMed ID: 11981749 [TBL] [Abstract][Full Text] [Related]
27. [Case for the clinical picture of hemochromatosis]. Auerswald W; Kupetz GW Z Arztl Fortbild (Jena); 1970 Sep; 64(18):947-9. PubMed ID: 5486171 [No Abstract] [Full Text] [Related]
28. Hereditary hemochromatosis: a case study and review. Laudicina RJ; Legrys VA Clin Lab Sci; 2001; 14(3):196-208; quiz 220-2. PubMed ID: 11517631 [TBL] [Abstract][Full Text] [Related]
29. Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease. Giambattistelli F; Bucossi S; Salustri C; Panetta V; Mariani S; Siotto M; Ventriglia M; Vernieri F; Dell'acqua ML; Cassetta E; Rossini PM; Squitti R Neurobiol Aging; 2012 Aug; 33(8):1633-41. PubMed ID: 21514009 [TBL] [Abstract][Full Text] [Related]
30. [Molecular genetics of hemochromatosis]. David V; Jouanolle AM; Fergelot P; Brissot P; Deugnier Y; Le Gall JY Ann Endocrinol (Paris); 1999 Sep; 60(3):204-9. PubMed ID: 10520411 [TBL] [Abstract][Full Text] [Related]
31. Nephrogenic diabetes insipidus associated with hemochromatosis. Okumura A; Kondo K; Hirai C; Nishimura H; Tamai H; Kawarazaki F; Ichikawa M; Mizuno M; Oiso Y; Yamamoto M Am J Kidney Dis; 2002 Aug; 40(2):403-6. PubMed ID: 12148115 [TBL] [Abstract][Full Text] [Related]
32. The relationship between iron overload, clinical symptoms, and age in 410 patients with genetic hemochromatosis. Adams PC; Deugnier Y; Moirand R; Brissot P Hepatology; 1997 Jan; 25(1):162-6. PubMed ID: 8985284 [TBL] [Abstract][Full Text] [Related]
33. Arthropathy in juvenile hemochromatosis. Vaiopoulos G; Papanikolaou G; Politou M; Jibreel I; Sakellaropoulos N; Loukopoulos D Arthritis Rheum; 2003 Jan; 48(1):227-30. PubMed ID: 12528123 [TBL] [Abstract][Full Text] [Related]
34. Sudden cardiac death in hereditary hemochromatosis: an underestimated cause of death? Klintschar M; Stiller D Int J Legal Med; 2004 Jun; 118(3):174-7. PubMed ID: 15133680 [TBL] [Abstract][Full Text] [Related]
35. Familial hemochromatosis; with comments on adrenal function in hemochromatosis. ROGERS WF Am J Med Sci; 1950 Nov; 220(5):530-37. PubMed ID: 14783122 [No Abstract] [Full Text] [Related]
36. Diagnosis and management of hereditary hemochromatosis. Salgia RJ; Brown K Clin Liver Dis; 2015 Feb; 19(1):187-98. PubMed ID: 25454304 [TBL] [Abstract][Full Text] [Related]
37. Revisiting hereditary hemochromatosis: current concepts and progress. Yen AW; Fancher TL; Bowlus CL Am J Med; 2006 May; 119(5):391-9. PubMed ID: 16651049 [TBL] [Abstract][Full Text] [Related]
38. Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features. Sham RL; Phatak PD; West C; Lee P; Andrews C; Beutler E Blood Cells Mol Dis; 2005; 34(2):157-61. PubMed ID: 15727899 [TBL] [Abstract][Full Text] [Related]
39. [Joint diseases as the early clinical symptom of hemochromatosis]. Walther B; Zönnchen B; Hehlmann R; Schattenkirchner M Fortschr Med; 1981 Mar; 99(10):321-5. PubMed ID: 7216095 [TBL] [Abstract][Full Text] [Related]