Cargando…
The impact of H63D HFE gene carriage on hemoglobin and iron status in children
The molecular mechanism that regulates iron homeostasis is based on a network of signals, which reflect on the iron requirements of the body. Hereditary hemochromatosis is a heterogenic metabolic syndrome which is due to unchecked transfer of iron into the bloodstream and its toxic effects on parenc...
Autores principales: | Barbara, Kaczorowska-Hac, Marcin, Luszczyk, Jedrzej, Antosiewicz, Wieslaw, Ziolkowski, Elzbieta, Adamkiewicz-Drozynska, Malgorzata, Mysliwiec, Ewa, Milosz, Jacek, Kaczor Jan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5093215/ https://www.ncbi.nlm.nih.gov/pubmed/27553379 http://dx.doi.org/10.1007/s00277-016-2792-x |
Ejemplares similares
-
HFE Gene Mutations and Iron Status in 100 Healthy Polish Children
por: Kaczorowska-Hac, Barbara, et al.
Publicado: (2017) -
Reduction of Skeletal Muscle Power in Adolescent Males Carrying H63D Mutation in the HFE Gene
por: Luszczyk, Marcin, et al.
Publicado: (2017) -
HFE protein impact on iron metabolism
por: Kaczorowska-Hać, Barbara, et al.
Publicado: (2017) -
Parental knowledge and metabolic control of children and young adults with type 1 diabetes
por: Stefanowicz, Anna, et al.
Publicado: (2016) -
The first reported case of G6PD deficiency due to Seoul mutation in Poland
por: Kaczorowska-Hac, Barbara, et al.
Publicado: (2013)