Maria-isabel Carralero-Moreno
Madrid, MD, Spain
Last Updated: 09/26/2026
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Found 9 publications
Juvenile Hemochromatosis due to a Homozygous Variant in the HJV Gene.
Journal: Case reports in pediatrics
Published: November 24, 2021
Missense variants in ALAS2 gene in five patients.
Journal: International journal of laboratory hematology
Published: July 19, 2018
Clinical and genetic features of congenital dyserythropoietic anemia (CDA).
Journal: European journal of haematology
Published: June 11, 2018
A case of congenital dyserythropoietic anemia type IV.
Journal: Clinical case reports
Published: July 28, 2016
Sideroblastic anemia: functional study of two novel missense mutations in ALAS2.
Journal: Molecular genetics & genomic medicine
Published: September 17, 2015
Pediatric Ferroportin Disease.
Journal: Journal of pediatric gastroenterology and nutrition
Published: March 06, 2015
A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro.
Journal: American journal of hematology
Published: July 30, 2013
Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis.
Journal: Gene
Published: July 05, 2012
The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload.
Journal: British journal of haematology
Published: February 09, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026