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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1953 1
1976 1
1978 1
1989 2
1990 1
1991 1
1992 2
1993 1
1996 1
1997 1
1999 2
2001 1
2002 1
2003 3
2004 1
2006 1
2007 1
2008 3
2009 3
2010 1
2011 1
2015 1
2016 1
2017 1
2019 1
2020 2
2021 2
2022 3
2024 0

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40 results

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Page 1
Dietary and Sentinel Factors Leading to Hemochromatosis.
Oh CK, Moon Y. Oh CK, et al. Nutrients. 2019 May 10;11(5):1047. doi: 10.3390/nu11051047. Nutrients. 2019. PMID: 31083351 Free PMC article. Review.
Although the mechanistic association to diet-linked etiologies can be complicated, the stress sentinels are pivotally involved in the pathological processes of secondary hemochromatosis in response to iron excess and other external stresses. Moreover, the mutations …
Although the mechanistic association to diet-linked etiologies can be complicated, the stress sentinels are pivotally involved in the pathol …
The treatment of secondary hemochromatosis.
Gattermann N. Gattermann N. Dtsch Arztebl Int. 2009 Jul;106(30):499-504, I. doi: 10.3238/arztebl.2009.0499. Epub 2009 Jul 24. Dtsch Arztebl Int. 2009. PMID: 19727383 Free PMC article. Review.
BACKGROUND: Because secondary hemochromatosis is due to hereditary or acquired anemia, phlebotomy is not a suitable means of removing excess iron in this situation. ...METHODS: Selective review of the literature. RESULTS: Disorders causing secondary hemoch …
BACKGROUND: Because secondary hemochromatosis is due to hereditary or acquired anemia, phlebotomy is not a suitable means of r …
Comparing Care of the Primary and Secondary Hemochromatosis Patients.
Becker S. Becker S. J Infus Nurs. 2020 Mar/Apr;43(2):65-69. doi: 10.1097/NAN.0000000000000358. J Infus Nurs. 2020. PMID: 32106193
Hemochromatosis is an imbalance of excessive serum iron and is a life-threatening condition if left untreated. Due to different causes, primary and secondary hemochromatosis have different patient care considerations for the infusion nurse. ...
Hemochromatosis is an imbalance of excessive serum iron and is a life-threatening condition if left untreated. Due to different causes, prim …
Iron deficiency and overload.
Beutler E, Hoffbrand AV, Cook JD. Beutler E, et al. Hematology Am Soc Hematol Educ Program. 2003:40-61. doi: 10.1182/asheducation-2003.1.40. Hematology Am Soc Hematol Educ Program. 2003. PMID: 14633776 Review.
Victor Hoffbrand discusses the management of iron storage disease by chelation therapy, treatment that is usually reserved for patients with secondary hemochromatosis such as occurs in the thalassemias and in patients with transfusion requirements due to myelodyspla …
Victor Hoffbrand discusses the management of iron storage disease by chelation therapy, treatment that is usually reserved for patients with …
Treatment of chronic iron overload.
Kirking MH. Kirking MH. Clin Pharm. 1991 Oct;10(10):775-83. Clin Pharm. 1991. PMID: 1742962 Review.
Chronic iron overload is classified as primary or secondary hemochromatosis. In primary hemochromatosis a genetic defect in iron metabolism results in increased absorption of iron from the gastrointestinal tract. The excess iron in secondary hemochromatosi …
Chronic iron overload is classified as primary or secondary hemochromatosis. In primary hemochromatosis a genetic defect in ir …
Iron overload cardiomyopathy: Using the latest evidence to inform future applications.
Kumfu S, Chattipakorn SC, Chattipakorn N. Kumfu S, et al. Exp Biol Med (Maywood). 2022 Apr;247(7):574-583. doi: 10.1177/15353702221076397. Epub 2022 Feb 7. Exp Biol Med (Maywood). 2022. PMID: 35130741 Free PMC article. Review.
Iron overload can be the result of either dysregulated iron metabolism in the case of hereditary hemochromatosis or repeated blood transfusions in the case of secondary hemochromatosis (e.g. in beta-thalassemia and sickle cell anemia patients). ...
Iron overload can be the result of either dysregulated iron metabolism in the case of hereditary hemochromatosis or repeated blood transfusi …
Hemochromatosis and Hepatocellular Carcinoma Secondary to Immunoglobulin G4-Related Disease with Hepatopathy: A Case Report.
Kanaka S, Kawano Y, Yokomuro S, Ando F, Itokawa N, Hatori T, Matsumoto K, Zen Y, Miyashita M, Yoshida H. Kanaka S, et al. J Nippon Med Sch. 2021 May 12;88(2):138-144. doi: 10.1272/jnms.JNMS.2021_88-306. Epub 2020 Aug 1. J Nippon Med Sch. 2021. PMID: 32741904 Free article.
Here we report the first case of secondary hemochromatosis and hepatocellular carcinoma (HCC) developing from IgG4-hepatopathy. ...However, extensive siderosis consistent with hemochromatosis was unexpectedly noted. These findings suggest that secondary he …
Here we report the first case of secondary hemochromatosis and hepatocellular carcinoma (HCC) developing from IgG4-hepatopathy …
Iron as a co-morbid factor in nonhemochromatotic liver disease.
Bonkovsky HL, Lambrecht RW, Shan Y. Bonkovsky HL, et al. Alcohol. 2003 Jun;30(2):137-44. doi: 10.1016/s0741-8329(03)00127-7. Alcohol. 2003. PMID: 12957298 Review.
Heavy iron overload, in both primary and secondary hemochromatosis, may cause fibrosis of parenchymal organs, especially the liver. ...
Heavy iron overload, in both primary and secondary hemochromatosis, may cause fibrosis of parenchymal organs, especially the l …
Hepatic injury in chronic iron overload. Role of lipid peroxidation.
Bacon BR, Britton RS. Bacon BR, et al. Chem Biol Interact. 1989;70(3-4):183-226. doi: 10.1016/0009-2797(89)90045-8. Chem Biol Interact. 1989. PMID: 2663196 Review.
In both hereditary hemochromatosis and in the various forms of secondary hemochromatosis, there is a pathologic expansion of body iron stores due mainly to an increase in absorption of dietary iron. ...Evidence for hepatotoxicity due to iron has been provided by sev …
In both hereditary hemochromatosis and in the various forms of secondary hemochromatosis, there is a pathologic expansion of b …
Hematopoietic Cell Transplantation for Congenital Dyserythropoietic Anemia: A Report from the Pediatric Transplant and Cellular Therapy Consortium.
Rangarajan HG, Stanek JR, Abdel-Azim H, Modi A, Haight A, McKinney CM, McKeone DJ, Buchbinder DK, Katsanis E, Abusin GA, Ahmed I, Law J, Silva JG, Mallhi KK, Burroughs LM, Shah N, Shaw PJ, Greiner R, Shenoy S, Pulsipher MA, Abu-Arja R. Rangarajan HG, et al. Transplant Cell Ther. 2022 Jun;28(6):329.e1-329.e9. doi: 10.1016/j.jtct.2022.03.007. Epub 2022 Mar 11. Transplant Cell Ther. 2022. PMID: 35288346 Free article.
Hematopoietic cell transplantation (HCT) is the sole curative option for congenital dyserythropoietic anemia (CDA), a rare type of hemolytic anemia characterized by anemia, ineffective erythropoiesis, and secondary hemochromatosis. In this retrospective multicenter …
Hematopoietic cell transplantation (HCT) is the sole curative option for congenital dyserythropoietic anemia (CDA), a rare type of hemolytic …
40 results