Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Inés Hernández-Rodríguez"'
Autor:
Lourdes Méndez-Mora, Maria Cabello-Fusarés, Josep Ferré-Torres, Carla Riera-Llobet, Elena Krishnevskaya, Claudia Trejo-Soto, Salvador Payán-Pernía, Inés Hernández-Rodríguez, Cristian Morales-Indiano, Tomas Alarcón, Joan-Lluis Vives-Corrons, Aurora Hernandez-Machado
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
The purpose of this work is to develop a hematocrit-independent method for the detection of beta-thalassemia trait (β-TT) and iron deficiency anemia (IDA), through the rheological characterization of whole blood samples from different donors. The re
Externí odkaz:
https://doaj.org/article/2e10c3a54ec047dbbbc316d51b12224d
Publikováno v:
Medicina Clínica. 158:221-228
Iron deficiency anaemia is highly prevalent worldwide. In the surgical patient, anaemia of any cause implies higher morbidity and mortality in the post-operative period. This is especially important in patients with peripheral artery disease, as they
Publikováno v:
Medicina clinica.
Publikováno v:
Medicina Clínica. 160:372
Autor:
Inés Hernández-Rodríguez, Ángel F. Remacha Sevilla, Elena Krishnevskaya, Vives-Corrons Jl, Isabel Badell, Salvador Payán-Pernía
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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Red blood cell (RBC) morphology is, in general, the key diagnostic feature for hereditary spherocytosis (HS) and hereditary elliptocytosis (HE). However, in hereditary pyropoikilocytosis (HPP), the severe clinical form of HE, the morphological diagno
Publikováno v:
Medicina clinica. 158(5)
Iron deficiency anaemia is highly prevalent worldwide. In the surgical patient, anaemia of any cause implies higher morbidity and mortality in the post-operative period. This is especially important in patients with peripheral artery disease, as they
Autor:
Vives-Corrons Jl, Salvador Payán‐Pernía, Ángel F. Remacha Sevilla, Marta Serra Ferrer, Cristian Morales-Indiano, Elena Krishnevskaya, Águeda Ancochea Serra, Inés Hernández-Rodríguez
Publikováno v:
International journal of laboratory hematology. 43(2)
Autor:
Ana Muntañola, Guillermo Villacampa, José Ángel Hernández-Rivas, Rosalía Alonso, Fátima Mirás, Santiago Osorio, Mónica Baile, Patricia Baltasar, Javier López Jiménez, Ines Hernandez-Rodriguez, Susana Valenciano, Ana Alfayate, Eva Gimeno, Abelardo Bárez, Ana C. Oliveira, Rosalía Riaza, Pilar Romero, Julio Delgado, Lucrecia Yáñez, Amaya Zabalza, Ana Torres, Mª Isabel Gómez-Roncero, Marta Crespo, Raúl Córdoba, Juan José Mateos-Mazón, Sonia Pérez, Rafael Andreu, Jorge Labrador, Mª Elena Ruiz, César Andrés Velasquez, Mª José Terol, Raquel Santiago, Mª Jesús Vidal, Fiz Campoy García, Lucía Villalón, Begoña S. Muiña, Joan Alfons Soler, Cristina Seri, Mª José Sánchez, Amalia Cuesta, Rafael Ramos, Adrián Sánchez-Montalvá, Isabel Ruiz-Camps, Marcos González, Pau Abrisqueta, Francesc Bosch, of the GELLC (Grupo Español de Leucemia Linfática Crónica)
Publikováno v:
Experimental Hematology & Oncology, Vol 9, Iss 1, Pp 1-4 (2020)
Externí odkaz:
https://doaj.org/article/3cb4c5fec4404b34821a7fef7650fb2d
Akademický článek
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Autor:
Ferran Celma Nos, Gonzalo Hernández, Xènia Ferrer-Cortès, Ines Hernandez-Rodriguez, Begoña Navarro-Almenzar, José Luis Fuster, Mar Bermúdez Cortés, Santiago Pérez-Montero, Cristian Tornador, Mayka Sanchez
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 11, p 5451 (2021)
Hereditary hyperferritinemia-cataract syndrome (HHCS) is a rare disease characterized by high serum ferritin levels, congenital bilateral cataracts, and the absence of tissue iron overload. This disorder is produced by mutations in the iron responsiv
Externí odkaz:
https://doaj.org/article/c6c64e2c3b3d4d4fabe1a6a125f68892