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Mayka Sanchez

Showing results (21-30 of 28) with videos related to

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Human Mutation|August 27, 2014
Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studiesLuigia De Falco, Laura Silvestri, Caroline Kannengiesser, et al.
Patient Education and Counseling|May 27, 2014
The importance of the general practitioner as an information source for patients with hereditary haemochromatosisEmerência Teixeira, Júlio Borlido-Santos, Pierre Brissot, et al.
Hemasphere|July 16, 2024
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Hepatology International|March 29, 2018
Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotypePaul Adams, Albert Altes, Pierre Brissot, et al.
Nature Metabolism|December 14, 2023
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotypeMate Maus, Vanessa López-Polo, Lidia Mateo, et al.
Journal of Hepatology|March 19, 2026
Characterization of ferroportin disease and SLC40A1-related hemochromatosis - Results from the EASL non-HFE registryMaria Rosina Troppmair, Andrea Ricci, Stefania Scarlini, et al.
International Journal of Molecular Sciences|April 3, 2020
Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early DiagnosisMarc Vila Cuenca, Giacomo Marchi, Anna Barqué, et al.
Haematologica|July 21, 2018
The phenotypic spectrum of germline <i>YARS2</i> variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2Lisa G Riley, Matthew M Heeney, Joëlle Rudinger-Thirion, et al.
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Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Human Mutation|August 27, 2014
Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studiesLuigia De Falco, Laura Silvestri, Caroline Kannengiesser, et al.
Patient Education and Counseling|May 27, 2014
The importance of the general practitioner as an information source for patients with hereditary haemochromatosisEmerência Teixeira, Júlio Borlido-Santos, Pierre Brissot, et al.
Hemasphere|July 16, 2024
Recommendations for diagnosis, treatment, and prevention of iron deficiency and iron deficiency anemiaAchille Iolascon, Immacolata Andolfo, Roberta Russo, et al.
Hepatology International|March 29, 2018
Therapeutic recommendations in HFE hemochromatosis for p.Cys282Tyr (C282Y/C282Y) homozygous genotypePaul Adams, Albert Altes, Pierre Brissot, et al.
Nature Metabolism|December 14, 2023
Iron accumulation drives fibrosis, senescence and the senescence-associated secretory phenotypeMate Maus, Vanessa López-Polo, Lidia Mateo, et al.
Journal of Hepatology|March 19, 2026
Characterization of ferroportin disease and SLC40A1-related hemochromatosis - Results from the EASL non-HFE registryMaria Rosina Troppmair, Andrea Ricci, Stefania Scarlini, et al.
International Journal of Molecular Sciences|April 3, 2020
Genetic and Clinical Heterogeneity in Thirteen New Cases with Aceruloplasminemia. Atypical Anemia as a Clue for an Early DiagnosisMarc Vila Cuenca, Giacomo Marchi, Anna Barqué, et al.
Haematologica|July 21, 2018
The phenotypic spectrum of germline <i>YARS2</i> variants: from isolated sideroblastic anemia to mitochondrial myopathy, lactic acidosis and sideroblastic anemia 2Lisa G Riley, Matthew M Heeney, Joëlle Rudinger-Thirion, et al.
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