Pediatric Ferroportin Disease von Galicia‐Poblet, Gonzalo, Cid‐París, Ester, López‐Andrés, Nerea, Losada‐Pajares, Alba, Jurado‐López, Juan‐Carlos, Moreno‐Carralero, María‐Isabel, Morán‐Jiménez, María‐Josefa

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Microcytic anemia in a pregnant woman: beyond iron deficiency von Rollón, Noelia, Fernández-Jiménez, María Cristina, Moreno-Carralero, María Isabel, Murga-Fernández, María José, Morán-Jiménez, María Josefa

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The homozygous mutation G75R in the human SLC11A2 gene leads to microcytic anaemia and iron overload von Barrios, Marta, Moreno-Carralero, María-Isabel, Cuadrado-Grande, Nuria, Baro, María, Vivanco, José-Luis, Morán-Jiménez, María-Josefa

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Hepcidin treatment in Hfe−/− mice diminishes plasma iron without affecting erythropoiesis von Morán-Jiménez, María-Josefa, Méndez, Manuel, Santiago, Begoña, Rodríguez-García, María-Elena, Moreno-Carralero, María-Isabel, Sánchez-Lucío, Ana-Cristina, Grau, Montserrat, Enríquez-de-Salamanca, Rafael

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Iron supplementation in mouse expands cellular innate defences in spleen and defers lethal malaria infection von Azcárate, Isabel G., Sánchez-Jaut, Sandra, Marín-García, Patricia, Linares, María, Pérez-Benavente, Susana, García-Sánchez, Marta, Uceda, Javier, Kamali, Ali N., Morán-Jiménez, María-Josefa, Puyet, Antonio, Diez, Amalia, Bautista, José M.

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Smoking but not homozygosity for CYP1A2 g-163A allelic variant leads to earlier disease onset in patients with sporadic porphyria cutanea tarda von Fontanellas, Antonio, Martínez-Fresno, María, Garrido-Astray, María Concepción, Perucho, Teresa, Morán-Jiménez, María-Josefa, García-Bravo, María, Méndez, Manuel, Poblete-Gutiérrez, Pamela, Frank, Jorge, Henriques-Gil, Nuno, De Salamanca, Rafael Enríquez

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Two novel mutations in the SLC40A1 and HFE genes implicated in iron overload in a Spanish man von del‐Castillo‐Rueda, Alejandro, Moreno‐Carralero, María‐Isabel, Álvarez‐Sala‐Walther, Luis‐Antonio, Cuadrado‐Grande, Nuria, Enríquez‐de‐Salamanca, Rafael, Méndez, Manuel, Morán‐Jiménez, María‐Josefa

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Mutations in the HFE, TFR2, and SLC40A1 genes in patients with hemochromatosis von del-Castillo-Rueda, Alejandro, Moreno-Carralero, María-Isabel, Cuadrado-Grande, Nuria, Álvarez-Sala-Walther, Luis-Antonio, Enríquez-de-Salamanca, Rafael, Méndez, Manuel, Morán-Jiménez, María-Josefa

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Familial porphyria cutanea tarda in Spain: Characterization of eight novel mutations in the UROD gene and haplotype analysis of the common p.G281E mutation von Gómez-Abecia, Sara, Morán-Jiménez, María-Josefa, Ruiz-Casares, Eva, Henriques-Gil, Nuno, García-Pastor, Inmaculada, Garrido-Astray, María-Concepción, Enríquez de Salamanca, Rafael, Méndez, Manuel

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Molecular analysis of the UROD gene in 17 Argentinean patients with familial porphyria cutanea tarda: Characterization of four novel mutations von Méndez, Manuel, Rossetti, María Victoria, Gómez-Abecia, Sara, Morán-Jiménez, María-Josefa, Parera, Victoria, Batlle, Alcira, Enríquez de Salamanca, Rafael

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The hereditary hyperferritinemia–cataract syndrome: a family study von Álvarez-Coca-González, Javier, Moreno-Carralero, María-Isabel, Martínez-Pérez, Jorge, Méndez, Manuel, García-Ros, Marta, Morán-Jiménez, María-Josefa

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Bone marrow-derived cells promote liver regeneration in mice with erythropoietic protoporphyria von García-Bravo, María, Morán-Jiménez, María-Josefa, Quintana-Bustamante, Oscar, Méndez, Manuel, Gutiérrez-Vera, Inmaculada, Bueren, Juan, Salido, Eduardo, Segovia, José-Carlos, Fontanellas, Antonio, de Salamanca, Rafael Enríquez

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Mutations in HFE and TFR2 genes in a Spanish patient with hemochromatosis von Rueda, Alejandro del Castillo, Grande, Nuria Cuadrado, Fernández, Emilio Alvarez, Enríquez de Salamanca, Rafael, Sala, Luis Antonio Alvarez, Jiménez, María Josefa Morán

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Bone marrow transplantation into hemochromatotic mice decreases hepatic and duodenal iron overload von Morán-Jiménez, María-Josefa, García-Bravo, María, Méndez, Manuel, Gutiérrez-Vera, Inmaculada, Grau, Montserrat, Navarro-Ordoñez, Susana, Fontanellas, Antonio, Enríquez-de-Salamanca, Rafael

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A novel mutation in the SLC40A1 gene associated with reduced iron export in vitro von Moreno‐Carralero, María‐Isabel, Muñoz‐Muñoz, Juan‐Antonio, Cuadrado‐Grande, Nuria, López‐Rodríguez, Rafaela, José Hernández‐Alfaro, María, del‐Castillo‐Rueda, Alejandro, Enríquez‐de‐Salamanca, Rafael, Méndez, Manuel, Morán‐Jiménez, María‐Josefa

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Hepcidin-Induced Endocytosis of Ferroportin Is Dependent on Ferroportin Ubiquitination von Qiao, Bo, Sugianto, Priscilla, Fung, Eileen, del-Castillo-Rueda, Alejandro, Moran-Jimenez, Maria-Josefa, Ganz, Tomas, Nemeth, Elizabeta

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Hereditary hyperferritinemia cataract syndrome in four patients with mutations in the IRE of the FTL gene von Muñoz-Muñoz, J, Cuadrado-Grande, N, Moreno-Carralero, M-I, Hoyos-Sanabria, B, Manubes-Guarch, A, González, A-F, Tejada-Palacios, P, del-Castillo-Rueda, A, Morán-Jiménez, M-J

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The homozygous mutation G 75 R in the human SLC11A2 gene leads to microcytic anaemia and iron overload von Barrios, Marta, Moreno‐Carralero, María‐Isabel, Cuadrado‐Grande, Nuria, Baro, María, Vivanco, José‐Luis, Morán‐Jiménez, María‐Josefa

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MUTATIONS IN HFE AND TFR2 GENES IN A SPANISH PATIENT WITH HEMOCHROMATOSIS von del Castillo-Rueda, Alejandro, Cuadrado-Grande, Nuria, Álvarez-Fernández, Emilio, Morán-Jiménez, María-Josefa

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Two novel mutations in the SLC40A1 and HFE genes implicated in iron overload in a Spanish man: Novel mutations in SLC40A1 and HFE von del-Castillo-Rueda, Alejandro, Moreno-Carralero, María-Isabel, Álvarez-Sala-Walther, Luis-Antonio, Cuadrado-Grande, Nuria, Enríquez-de-Salamanca, Rafael, Méndez, Manuel, Morán-Jiménez, María-Josefa

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