Publications by authors named "Ines Hernandez-Rodriguez"

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The role of genetic testing in accurate diagnosis of X-linked sideroblastic anemia: novel ALAS2 mutations and the impact of X-chromosome inactivation.
Daniel Jové-Solavera, Marta Rámila, Xènia Ferrer-Cortés, Mireia Olivella, Veronica Venturi

Sci Rep· April 2025

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Prognostic significance of mutation type and chromosome fragility in Fanconi anemia.
María José Ramírez, Roser Pujol, Jordi Minguillón, Massimo Bogliolo, Ilaria Persico

Am J Hematol· February 2025

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Characterization of South-East Asian ovalocytosis using osmotic gradient ektacytometry.
Marta Canelo-Vilaseca, Inés Hernández-Rodríguez, José-Tomás Navarro

Med Clin (Barc)· January 2024

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Iron overload refractory to phlebotomy in a patient with type 1 hereditary hemochromatosis.
Marta Canelo-Vilaseca, Josep-Maria Ribera, Inés Hernández-Rodríguez

Med Clin (Barc)· April 2023

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Monocyte subset analysis in the presence of paroxismal nocturnal hemoglobinuria. A case report.
Merce Aren, Ines Hernandez-Rodriguez, Blanca Xicoy, Lurdes Zamora, Marc Sorigue

Int J Lab Hematol· December 2022

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Peripheral arterial disease and anaemia.
Carlos Esteban, Inés Hernández-Rodríguez

Med Clin (Barc)· March 2022

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Red cell ektacytometry in two patients with chronic hemolytic anemia and three new α-spectrin variants.
Joan-Lluis Vives-Corrons, Elena Krishnevskaya, Inés Hernández-Rodriguez, Salvador Payán-Pernia, Ángel F Remacha Sevilla

Ann Hematol· March 2022

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New Mutations in and Genes Causing Non -Related Hereditary Hemochromatosis.
Gonzalo Hernández, Xenia Ferrer-Cortès, Veronica Venturi, Melina Musri, Martin Floor Pilquil

Genes (Basel)· December 2021

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Blood Rheological Characterization of β-Thalassemia Trait and Iron Deficiency Anemia Using Front Microrheometry.
Lourdes Méndez-Mora, Maria Cabello-Fusarés, Josep Ferré-Torres, Carla Riera-Llobet, Elena Krishnevskaya

Front Physiol· October 2021

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Hereditary Hyperferritinemia Cataract Syndrome: Ferritin L Gene and Physiopathology behind the Disease-Report of New Cases.
Ferran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, Ines Hernandez-Rodriguez, Begoña Navarro-Almenzar

Int J Mol Sci· May 2021

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Distinguishing iron deficiency from beta-thalassemia trait by new generation ektacytometry.
Elena Krishnevskaya, Salvador Payán-Pernía, Inés Hernández-Rodríguez, Ángel F Remacha Sevilla, Águeda Ancochea Serra

Int J Lab Hematol· April 2021

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Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry.
Joan-Lluis Vives-Corrons, Elena Krishnevskaya, Ines Hernandez Rodriguez, Agueda Ancochea

Int J Hematol· February 2021

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Clinical characteristics and outcome of SARS-CoV-2 infection in admitted patients with chronic lymphocytic leukemia from a single European country.
Ana Muntañola, Guillermo Villacampa, José Ángel Hernández-Rivas, Rosalía Alonso, Fátima Mirás, Ines Hernandez-Rodriguez

Exp Hematol Oncol· December 2020

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CoDysAn: A Telemedicine Tool to Improve Awareness and Diagnosis for Patients With Congenital Dyserythropoietic Anemia.
Cristian Tornador, Edgar Sánchez-Prados, Beatriz Cadenas, Roberta Russo, Veronica Venturi

Front Physiol· September 2019

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L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases.
Beatriz Cadenas, Josep Fita-Torró, Mar Bermúdez-Cortés, Inés Hernandez-Rodriguez, José Luis Fuster

Pharmaceuticals (Basel)· January 2019

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