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European Journal of Investigation in Health, Psychology and Education
|
April 27, 2026
Higher Education as a Driver for the Humanization of Pediatric Pain Care (HUPEDCARE): Protocol of a Multicenter Study
Sagrario Gómez-Cantarino, Henrique Ciabotti Elias, Miriam Hermida-Mota, et al.
Human Mutation
|
April 26, 2020
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia
Diana Gallego, Fátima Leal, Alejandra Gámez, et al.
Journal of the American Geriatrics Society
|
December 11, 2021
Immunogenicity after 6 months of BNT162b2 vaccination in frail or disabled nursing home residents: The COVID-A Study
Sergio Salmerón Ríos, Elisa Belén Cortés Zamora, Almudena Avendaño Céspedes, et al.
Neuroradiology
|
June 6, 2022
Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders
Chiara Alfonsi, Christian Stephan-Otto, Elisenda Cortès-Saladelafont, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
October 24, 2025
MicroRNA whole-blood profiling in hospitalized patients with candidemia identified miR-125a-5p and miR-99b-5p as potential biomarkers for Candida albicans bloodstream infection
Silvio Ragozzino, Daniel Salete-Granado, Luis-Antonio Corchete, et al.
Journal of Clinical Medicine
|
November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment
Irene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
Revista Espanola De Geriatria Y Gerontologia
|
March 15, 2011
[Frailty and dependence in Albacete (FRADEA study): reasoning, design and methodology]
Pedro Abizanda Soler, Jesús López-Torres Hidalgo, Luis Romero Rizos, et al.
European Journal of Human Genetics : EJHG
|
January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program
Rosa Navarrete, Fátima Leal, Ana I Vega, et al.
Orphanet Journal of Rare Diseases
|
December 1, 2014
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases
Elena Martín-Hernández, Luis Aldámiz-Echevarría, Esperanza Castejón-Ponce, et al.
Clinical Genetics
|
January 18, 2019
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain
Celia Medrano, Ana Vega, Rosa Navarrete, et al.
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of 35
Search research articles
Search
Showing results (331-340 of 344) with videos related to
Sort By:
Page
of 35
European Journal of Investigation in Health, Psychology and Education
|
April 27, 2026
Higher Education as a Driver for the Humanization of Pediatric Pain Care (HUPEDCARE): Protocol of a Multicenter Study
Sagrario Gómez-Cantarino, Henrique Ciabotti Elias, Miriam Hermida-Mota, et al.
Human Mutation
|
April 26, 2020
Pathogenic variants of DNAJC12 and evaluation of the encoded cochaperone as a genetic modifier of hyperphenylalaninemia
Diana Gallego, Fátima Leal, Alejandra Gámez, et al.
Journal of the American Geriatrics Society
|
December 11, 2021
Immunogenicity after 6 months of BNT162b2 vaccination in frail or disabled nursing home residents: The COVID-A Study
Sergio Salmerón Ríos, Elisa Belén Cortés Zamora, Almudena Avendaño Céspedes, et al.
Neuroradiology
|
June 6, 2022
Volumetric study of brain MRI in a cohort of patients with neurotransmitter disorders
Chiara Alfonsi, Christian Stephan-Otto, Elisenda Cortès-Saladelafont, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
October 24, 2025
MicroRNA whole-blood profiling in hospitalized patients with candidemia identified miR-125a-5p and miR-99b-5p as potential biomarkers for Candida albicans bloodstream infection
Silvio Ragozzino, Daniel Salete-Granado, Luis-Antonio Corchete, et al.
Journal of Clinical Medicine
|
November 6, 2019
Genes and Variants Underlying Human Congenital Lactic Acidosis-From Genetics to Personalized Treatment
Irene Bravo-Alonso, Rosa Navarrete, Ana Isabel Vega, et al.
Revista Espanola De Geriatria Y Gerontologia
|
March 15, 2011
[Frailty and dependence in Albacete (FRADEA study): reasoning, design and methodology]
Pedro Abizanda Soler, Jesús López-Torres Hidalgo, Luis Romero Rizos, et al.
European Journal of Human Genetics : EJHG
|
January 11, 2019
Value of genetic analysis for confirming inborn errors of metabolism detected through the Spanish neonatal screening program
Rosa Navarrete, Fátima Leal, Ana I Vega, et al.
Orphanet Journal of Rare Diseases
|
December 1, 2014
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases
Elena Martín-Hernández, Luis Aldámiz-Echevarría, Esperanza Castejón-Ponce, et al.
Clinical Genetics
|
January 18, 2019
Clinical and molecular diagnosis of non-phosphomannomutase 2 N-linked congenital disorders of glycosylation in Spain
Celia Medrano, Ana Vega, Rosa Navarrete, et al.
Page
of 35