Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Fernando Ataúlfo González Fernández"'
Autor:
Silvia Escribano Serrat, Javier Cucharero Martín, Fiorella Medina Salazar, Estefanía Bolaños Calderón, Isabel Ortega Madueño, Celina Benavente Cuesta, Fernando Ataúlfo González Fernández
Publikováno v:
eJHaem, Vol 3, Iss 3, Pp 1073-1075 (2022)
Externí odkaz:
https://doaj.org/article/d92961f5e589443e95e1d0e3d976b6a1
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, 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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::224e9b94135a4a2f34ca9c749fdb7e0a
https://doi.org/10.1007/s00277-022-04837-4
https://doi.org/10.1007/s00277-022-04837-4
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::513e8dc637aa61529522a336feb17f60
https://doi.org/10.1136/jclinpath-2020-206812
https://doi.org/10.1136/jclinpath-2020-206812
Autor:
Andrés Felipe Melo Arias, Silvia Escrıbano Escribano Serrat, Marta Polo Zarzuela, Cristina García Sánchez, Miguel Gómez Álvarez, Eduardo Anguita, Celina Benavente Cuesta, Fernando Ataulfo González Fernández
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 2, Pp 113-115 (2024)
Externí odkaz:
https://doaj.org/article/c60d031dbc794b21b9f6b227d198ff33
Autor:
Silvia Escribano Serrat, Gonzalo Del Campo Balguerías, Jorge Martínez Nieto, Fiorella Medina Salazar, Celina Benavente Cuesta, Fernando Ataúlfo González Fernández
Publikováno v:
Annals of hematology. 101(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d10b4d33c0a17e6b4896ab5ac6b7185
https://pubmed.ncbi.nlm.nih.gov/35107608
https://pubmed.ncbi.nlm.nih.gov/35107608
Autor:
Paloma Ropero, Celina Benavente, Jorge M. Nieto, Ana Villegas, Fernando-Ataúlfo González Fernández
Publikováno v:
Clinical biochemistry. 92
Objective To describe a new mutation causing alpha thalassemia and its mechanism of action. Design and methods The propositus was a 37-year-old man who presented maintained microcytosis without iron deficiency. Molecular characterization was undertak
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c4654e06c0a7ee734e43a926ac79f95
https://pubmed.ncbi.nlm.nih.gov/33675809
https://pubmed.ncbi.nlm.nih.gov/33675809
Autor:
Paloma Ropero, María Paz Plaza, Alfonso Muriel, Lorena Abalo, Maria Teresa Tenorio, Marina Fernández-Escribano, María Sopeña, Juan-Manuel Alonso-Domínguez, Ana Jiménez-Martín, Jesús Villarrubia, Fernando-Ataúlfo González-Fernández, Francisco Javier López-Jiménez, Gemma Moreno, Fernando Cava, Félix de la Fuente-Gonzalo, Diego Velasco-Rodríguez, Jorge Martínez-Nieto
Publikováno v:
Journal of Clinical Pathology. 69:912-920
Background Haemoglobinopathies have spread owing to human migration, and the number of people needing diagnosis and management of these conditions is increasing. Clinicians need to accurately identify carriers and provide adequate genetic counselling
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf5e4876fa242ff4224b03cdd21dcd2
https://doi.org/10.1136/jclinpath-2015-203556
https://doi.org/10.1136/jclinpath-2015-203556
Autor:
Manuel Méndez, María-Isabel Moreno-Carralero, Adela-María Periago-Peralta, Angelina Lemes-Castellano, María-Pilar Ricard-Andrés, Saul Horta-Herrera, Marta Morado-Arias, Silvia de-la-Iglesia-Iñigo, Laura Llorente-González, María-Teresa Cedena-Romero, María-José Morán-Jiménez, Mariola Abio-Calvete, Fernando-Ataúlfo González-Fernández
Publikováno v:
European journal of haematology. 101(3)
Introduction Congenital dyserythropoietic anemias (CDA) are characterized by hyporegenerative anemia with inadequate reticulocyte values, ineffective erythropoiesis, and hemolysis. Distinctive morphology of bone marrow erythroblasts and identificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aebaa7bce4f5dac0111839ff42af4d64
https://pubmed.ncbi.nlm.nih.gov/29901818
https://pubmed.ncbi.nlm.nih.gov/29901818
Autor:
Jesús Villarrubia, Lorena Abalo, Paloma Ropero, Jorge Martínez-Nieto, Félix de la Fuente Gonzalo, María Sopeña, Fernando-Ataúlfo González-Fernández, Juan-Manuel Alonso-Domínguez, Fernando Cava, Diego Velasco-Rodríguez
Publikováno v:
Journal of Clinical Pathology. 69:149-154
To analyse the differences in reticulocyte indices between delta beta thalassaemia trait (δβ-TT), beta thalassaemia trait (β-TT) and iron deficiency anaemia (IDA), and to correlate those differences with the physiopathological features of these th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e24af34685c8f7d4a3243cd52ee5d34
https://doi.org/10.1136/jclinpath-2015-203034
https://doi.org/10.1136/jclinpath-2015-203034