Juvenile haemochromatosis
Author:
Publisher
Elsevier BV
Subject
Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health
Reference30 articles.
1. Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review;Kong;Orphanet J Rare Dis,2019
2. Hepcidin regulates cellular iron efflux by binding to ferroportin and inducing its internalization;Nemeth;Science,2004
3. Inappropriate expression of hepcidin is associated with iron refractory anemia: implications for the anemia of chronic disease;Weinstein;Blood,2002
4. Mutations in HFE2 cause iron overload in chromosome 1q-linked juvenile hemochromatosis;Papanikolaou;Nat Genet,2004
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1. The Celtic Curse: Screening Children for Genetic Haemochromatosis;Comprehensive Child and Adolescent Nursing;2024-07-02
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3. Penetrance, cancer incidence and survival in HFE haemochromatosis—A population‐based cohort study;Liver International;2024-01-23
4. Haemochromatosis in children: A national retrospective cohort promoted by the A.I.E.O.P. (Associazione Italiana Emato‐Oncologia Pediatrica) study group;British Journal of Haematology;2023-11-21
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