Zobrazeno 1 - 10
of 6 348
pro vyhledávání: '"HEREDITARY HEMOCHROMATOSIS"'
Publikováno v:
JAAD Case Reports, Vol 50, Iss , Pp 30-32 (2024)
Externí odkaz:
https://doaj.org/article/d9596f8f601b4ea49befa5acd9b3c863
Akademický článek
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Autor:
Dongdong Li, Jinfeng Li, Hongkun Zhang, Qiuyu Zhu, Teng Wang, Wen Zhao, Shousong Zhao, Wei Li
Publikováno v:
Heliyon, Vol 10, Iss 7, Pp e28046- (2024)
Hereditary hemochromatosis (HH) is a disease characterized by disordered iron metabolism. It often involves mutations of the HFE gene, which encodes the homeostatic iron regulator protein (HFE), as well as mutations affecting hepcidin antimicrobial p
Externí odkaz:
https://doaj.org/article/8e3b989d153347dd8b5c551cca12d8b2
Publikováno v:
eJHaem, Vol 4, Iss 2, Pp 544-547 (2023)
Externí odkaz:
https://doaj.org/article/42cb21f7edfe4f34b47321d4247472a4
Autor:
Miller, Elizabeth M., author
Publikováno v:
Thicker Than Water : A Social and Evolutionary Study of Iron Deficiency in Women, 2023.
Externí odkaz:
https://doi.org/10.1093/oso/9780197665718.003.0002
Autor:
Michael Lockhart, Muhammad Ridhwaan Salehmohamed, Dileep Kumar, Anne Graham Cummiskey, Keat Cheah Seong, Seamus Sreenan, John McDermott
Publikováno v:
American Journal of Medicine Open, Vol 10, Iss , Pp 100046- (2023)
Aims: Hereditary hemochromatosis (HH) is the most common inherited disease in European populations. It is particularly common in people of Irish heritage, approximately 2% of whom will be at risk of iron overload as a result of human homoeostatic iro
Externí odkaz:
https://doaj.org/article/9fc4a41c8aa84699875cd22a7e619951
Autor:
María E. Mónaco, Natalia S. Alvarez Asensio, Cecilia Haro, Magdalena M. Terán, Miryam E. Ledesma Achem, Blanca A. Issé, Sandra S. Lazarte
Publikováno v:
Thalassemia Reports, Vol 13, Iss 1, Pp 113-121 (2023)
The human hemochromatosis protein HFE is encoded by the HFE gene and participates in iron regulation. The aim of this study was to detect the most frequent HFE gene mutations in a control population and in β-thalassemia trait (BTT) carriers, and to
Externí odkaz:
https://doaj.org/article/868eab3dc00040689dd7efd240c4d973
Autor:
Michał Świątczak, Katarzyna Rozwadowska, Katarzyna Sikorska, Krzysztof Młodziński, Agata Świątczak, Grzegorz Raczak, Ludmiła Daniłowicz-Szymanowicz
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundHereditary hemochromatosis (HH) is a genetic disease that leads to increased iron accumulation in several organs. Cardiomyocytes are highly susceptible to this damage owing to their high iron uptake, and cardiovascular complications account
Externí odkaz:
https://doaj.org/article/d29d4befe8344b7cbca537859cbcc86e
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
Nathalia Kersting, Juliana Cristine Fontana, Fabiane Pohlmann de Athayde, Fernanda Marcante Carlotto, Bruna Accorsi Machado, Cristiane da Silva Rodrigues de Araújo, Leo Sekine, Tor Gunnar Hugo Onsten, Sandra Leistner-Segal
Publikováno v:
Genetics and Molecular Biology, Vol 46, Iss 2 (2023)
Abstract Hereditary Hemochromatosis is a disorder characterized by iron deposition in several organs and hyperferritinemia. The most studied variants are linked to the HFE gene. In Brazil, surveys that characterize this population are scarce, with no
Externí odkaz:
https://doaj.org/article/1a09ab0882444a3894ef1ed68d9c6e8c