Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Jorge M. Nieto"'
Autor:
Marta Molina-Pérez, Jorge M. Nieto, Paloma Ropero Gradilla, Silvia Escribano Serrat, Miguel Gómez Álvarez, Horacio Gulino, Pablo Estival Monteliú, Antonio Chamorro Fernández, María Eva Mingot, José García Gala, María Cristina Vega Cabrera, Irene Amores Hernández, Juan Churruca Sarasqueta, Mónica Bonete Román, Ataulfo González Fernández, Ana Villegas, Celina Benavente Cuesta
Publikováno v:
HemaSphere, Vol 7, p e4031727 (2023)
Externí odkaz:
https://doaj.org/article/010ccd0b894f4807835377b02ac470f6
Autor:
Paloma Ropero, Fernando Ataúlfo González Fernández, Jorge M. Nieto, Williana Melissa Torres-Jiménez, Celina Benavente
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
ObjectivesTo verify with hematimetric data that the diagnosis and clinical grade of β-TI can be established when a triplication of alpha genes (αααanti 3.7) and heterozygous β-thalassemia coexist.Materials and MethodsRetrospective study in which
Externí odkaz:
https://doaj.org/article/0d431a33d3bd49f4ae7b9a467577ab04
Autor:
Paloma Ropero Gradilla, José María Raya, Fernando Ataúlfo González, Sara Rochas, Sara Ferrer-Benito, Jorge M. Nieto, Taida Martín-Santos, Marcelo Barrios, Lorena Gutiérrez-Murillo, Ana Villegas, Celina Benavente
Publikováno v:
Hemoglobin. 46:344-346
Autor:
Paloma Ropero, Fernando Ataúlfo González Fernández, Jorge M. Nieto, Valle Recasens, Ángeles Montañés, María José Murúzabal, María Sarasa, Cristina Fernández, Ana Villegas, Cuesta C. Benavente
Publikováno v:
Annals of Hematology. 101:1465-1471
Autor:
Celina Benavente Cuesta, Jorge M. Nieto, José Bartolomé Nieto Campuzano, Beatriz González Fernández, Ana Villegas, Dolores García Rocamora, Paloma Ropero, Fernando Ataulfo González Fernández
Publikováno v:
Annals of Laboratory Medicine
Autor:
Julio Del Rio, Cristina Pascual, Jorge M. Nieto, Maribel Diaz-Ricart, Ramón Salinas, Inés Gómez Seguí, Marta Fernández Docampo, Teresa Fidalgo
Publikováno v:
International Journal of Laboratory Hematology. 43:485-493
Introduction Thrombotic thrombocytopenic purpura (TTP) is a rare life-threatening thrombotic microangiopathy (TMA) characterized by the severe deficiency of ADAMTS13 activity ( Methods A comparison method was performed to compare HemosIL Acustar® wi
Autor:
Paloma Ropero, Celina Benavente, Yolanda González, Carmen Rodríguez-Vigil, Ana Villegas, Guillermo Hernández de Abajo, Angeles Montañés, Valle Recasens, Beatriz González Fernández, Fernando-Ataúlfo González-Fernández, Jorge M. Nieto
Publikováno v:
Journal of Clinical Pathology. 74:198-201
Screening of haemoglobinopathies is indicated for the detection of sickle cell anaemia; thus, neonates can benefit from early and adequate treatment that prevents neurological damage, reduces morbidity and mortality associated with the disease. These
Autor:
Jorge M. Nieto, Sara Rochas-López, Fernando A. González-Fernández, Ana Villegas-Martínez, Estefanía Bolaños-Calderón, Eduardo Salido-Fiérrez, Elena Cela, Jorge Huerta-Aragoneses, María Ordoñez-García, María J. Muruzábal-Sitges, Mariola Abio-Calvete, Julián Sevilla Navarro, Silvia de la Iglesia, Marta Morado, Sonsoles San Román-Pacheco, María L. Martín-Mateos, María V. Recasens-Flores, Celina Benavente-Cuesta, Paloma Ropero-Gradilla, null Members of the erithropatology working group
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 531
Hereditary anemia (HA) encloses a wide group of rare inherited disorders with clinical and hematologic overlaps that complicate diagnosis.A 48-gene panel was developed to diagnose HA by Next Generation Sequencing (NGS) in a large cohort of 165 patien
Autor:
Ana Villegas, Celina Benavente, Fernando A. González, Jaime Arbeteta, Paloma Ropero, Jorge M. Nieto, Beatriz González
Publikováno v:
Hemoglobin. 44:17-19
About 10.0% of α-thalassemia (α-thal) cases are due to point mutations, small deletions, or insertions of one or more bases on the α genes that can alter mRNA processing at the transcription, translation, or post-translation level; these cases are
Autor:
Jorge M. Nieto, Félix de la Fuente-Gonzalo, Paloma Ropero, Rafael Martínez, Ana Villegas, Fernando A. González
Publikováno v:
Annals of Hematology. 98:1537-1545
The hemoglobinopathies are a group of disorders passed down through families (inherited) in which there is abnormal production or structure of the hemoglobin molecule. They are among the most common inherited diseases around the world. Those that pro