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2. Postshunt hemochromatosis leading to cardiogenic shock in a patient presenting for orthotopic liver transplant: a case report. Hughes CG; Waldman JM; Barrios J; Robertson A Transplant Proc; 2009 Jun; 41(5):2000-2. PubMed ID: 19545779 [TBL] [Abstract][Full Text] [Related]
3. An autopsy case of pyruvate kinase deficiency anemia associated with severe hemochromatosis. Nagai H; Takazakura E; Oda H; Tsuji H; Terada Y; Makino H; Yamauchi H; Saitoh K Intern Med; 1994 Jan; 33(1):56-9. PubMed ID: 8180445 [TBL] [Abstract][Full Text] [Related]
5. Neonatal hemochromatosis--report of an autopsy case. Suh YL; Khang SK; Kim KN J Korean Med Sci; 1991 Sep; 6(3):267-72. PubMed ID: 1777132 [TBL] [Abstract][Full Text] [Related]
6. Multiple organ dysfunction in a 33-year-old woman due to hereditary hemochromatosis. Niihara Y; Brouwer DW; Cantos KA West J Med; 1995 Apr; 162(4):362-4. PubMed ID: 7747508 [No Abstract] [Full Text] [Related]
8. [-Cardiomyopathy as the cause of death in genetic hemochromatosis-]. von Herbay A; Niederau C; Pilichowska M; Reinecke P; Perings C; Vester E; Strohmeyer G; Häussinger D Z Gastroenterol; 1996 Mar; 34(3):178-82. PubMed ID: 8650971 [TBL] [Abstract][Full Text] [Related]
9. [Case of generalized hemochromatosis]. Vershinina KIa; Grinberg II Arkh Patol; 1987; 49(6):63-6. PubMed ID: 3662849 [TBL] [Abstract][Full Text] [Related]
10. Progressive hemochromatotic cardiomyopathy despite reversal of iron deposition after liver transplantation. Westra WH; Hruban RH; Baughman KL; Olson JL; Porterfield JK; Mitchell MC; Hutchins GM Am J Clin Pathol; 1993 Jan; 99(1):39-44. PubMed ID: 8422014 [TBL] [Abstract][Full Text] [Related]
11. Vibrio vulnificus septicemia in a patient with the hemochromatosis HFE C282Y mutation. Gerhard GS; Levin KA; Price Goldstein J; Wojnar MM; Chorney MJ; Belchis DA Arch Pathol Lab Med; 2001 Aug; 125(8):1107-9. PubMed ID: 11473471 [TBL] [Abstract][Full Text] [Related]
12. Fatal Cardiac Hemochromatosis in a Patient with Hereditary Spherocytosis. Fujino T; Inoue S; Katsuki S; Higo T; Ide T; Oda Y; Tsutsui H Int Heart J; 2018 Mar; 59(2):427-430. PubMed ID: 29563373 [TBL] [Abstract][Full Text] [Related]
13. Neonatal multiorgan failure due to ACAD9 mutation and complex I deficiency with mitochondrial hyperplasia in liver, cardiac myocytes, skeletal muscle, and renal tubules. Leslie N; Wang X; Peng Y; Valencia CA; Khuchua Z; Hata J; Witte D; Huang T; Bove KE Hum Pathol; 2016 Mar; 49():27-32. PubMed ID: 26826406 [TBL] [Abstract][Full Text] [Related]
14. [Hemochromatosis with a predominant lesion of the heart]. Iampol'skaia SA Arkh Patol; 1979; 41(4):58-61. PubMed ID: 444090 [TBL] [Abstract][Full Text] [Related]
15. [Autopsy case of hemochromatosis--with special reference to the non-iron-containing pigment (hemofuscin)]. Ihara N; Hagihara T; Kanazawa K; Nakano E; Kondo T Saishin Igaku; 1970 Dec; 25(12):2576-88. PubMed ID: 4924764 [No Abstract] [Full Text] [Related]