From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia C Krausz, A Riera-Escamilla, C Chianese, D Moreno-Mendoza, E Ars, ... Genetics in Medicine 21 (1), 189-194, 2019 | 47 | 2019 |
L-Ferritin: one gene, five diseases; from hereditary hyperferritinemia to hypoferritinemia—Report of new cases B Cadenas, J Fita-Torró, M Bermúdez-Cortés, I Hernandez-Rodriguez, ... Pharmaceuticals 12 (1), 17, 2019 | 28 | 2019 |
Characterization of hereditary red blood cell membranopathies using combined targeted next-generation sequencing and osmotic gradient ektacytometry JL Vives-Corrons, E Krishnevskaya, IH Rodriguez, A Ancochea International Journal of Hematology 113, 163-174, 2021 | 27 | 2021 |
Usefulness of IGH/TCR PCR studies in lymphoproliferative disorders with inconclusive clonality by flow cytometry J Ribera, L Zamora, J Junca, I Rodríguez, S Marcé, M Cabezón, F Millá Cytometry Part B: Clinical Cytometry 86 (1), 25-31, 2014 | 19 | 2014 |
Hidden myelodysplastic syndrome (MDS): A prospective study to confirm or exclude MDS in patients with anemia of uncertain etiology JM Bastida, O López‐Godino, A Vicente‐Sánchez, S Bonanad‐Boix, ... International journal of laboratory hematology 41 (1), 109-117, 2019 | 17 | 2019 |
Mobilization and engraftment of peripheral blood stem cells in healthy related donors> 55 years old C Motlló, JM Sancho, JR Grífols, J Juncà, M Morgades, A Ester, ... Cytotherapy 16 (3), 406-411, 2014 | 16 | 2014 |
Hereditary hyperferritinemia cataract syndrome: ferritin L gene and physiopathology behind the disease—report of new cases F Celma Nos, G Hernández, X Ferrer-Cortès, I Hernandez-Rodriguez, ... International Journal of Molecular Sciences 22 (11), 5451, 2021 | 13 | 2021 |
Clinical characteristics and outcome of SARS-CoV-2 infection in admitted patients with chronic lymphocytic leukemia from a single European country A Muntañola, G Villacampa, JÁ Hernández-Rivas, R Alonso, F Mirás, ... Experimental Hematology & Oncology 9, 1-4, 2020 | 12 | 2020 |
New Mutations in HFE2 and TFR2 Genes Causing Non HFE-Related Hereditary Hemochromatosis G Hernández, X Ferrer-Cortès, V Venturi, M Musri, MF Pilquil, PMM Torres, ... Genes 12 (12), 1980, 2021 | 9 | 2021 |
Distinguishing iron deficiency from beta-thalassemia trait by new generation ektacytometry E Krishnevskaya, S Payan-Pernia, I Hernandez-Rodriguez, ÁFR Sevilla, ... International journal of laboratory hematology 43 (2), e58-e60, 2021 | 8 | 2021 |
Blood rheological characterization of β-thalassemia trait and iron deficiency anemia using front microrheometry L Méndez-Mora, M Cabello-Fusarés, J Ferré-Torres, C Riera-Llobet, ... Frontiers in Physiology 12, 761411, 2021 | 6 | 2021 |
CoDysAn: a telemedicine tool to improve awareness and diagnosis for patients with congenital dyserythropoietic anemia C Tornador, E Sánchez-Prados, B Cadenas, R Russo, V Venturi, I Andolfo, ... Frontiers in Physiology 10, 459618, 2019 | 6 | 2019 |
Tu1925 Real-Life Experience With Golimumab in Ulcerative Colitis Patients According to Prior Anti-TNF Use C Taxonera, F Bertoletti, C Rodríguez, L Menchen, J Arribas, ... Gastroenterology 150 (4), S979, 2016 | 5 | 2016 |
Sobrecarga férrica refractaria a flebotomías en un paciente con hemocromatosis hereditaria tipo 1 M Canelo-Vilaseca, JM Ribera, I Hernández-Rodríguez Med. clín (Ed. impr.), 372-372, 2023 | 2 | 2023 |
Diffuse large B cell lymphoma associated with hemophagocytic syndrome I Rodriguez, J Grau, JM Sancho, JM Ribera Medicina Clinica 136 (2), 87-88, 2010 | 2 | 2010 |
Peripheral arterial disease and anaemia C Esteban, I Hernández-Rodríguez Medicina Clínica (English Edition) 158 (5), 221-228, 2022 | 1 | 2022 |
Characterization of South-East Asian ovalocytosis using osmotic gradient ektacytometry M Canelo-Vilaseca, I Hernández-Rodríguez, JT Navarro Medicina clinica 162 (1), 43, 2024 | | 2024 |
Caracterización de la ovalocitosis del sud-este asiático mediante ectacitometría de gradiente osmótico M Canelo-Vilaseca, I Hernández-Rodríguez, J Navarro Medicina Clínica 162 (1), 43-NA, 2024 | | 2024 |
P1480: CLINICAL AND GENETIC STUDY OF HEREDITARY SPHEROCYTOSIS IN THE SPANISH POPULATION. L Castilla, J Aspa, JM Nieto, ÁZ Cabrera, M Santiago, AG Feria, ... HemaSphere 7 (S3), e6313050, 2023 | | 2023 |
Iron overload refractory to phlebotomy in a patient with type 1 hereditary hemochromatosis M Canelo-Vilaseca, JM Ribera, I Hernández-Rodríguez Medicina clinica 160 (8), 372, 2023 | | 2023 |