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Nutrients|July 2, 2021
Evaluation of Body Composition, Physical Activity, and Food Intake in Patients with Inborn Errors of Intermediary MetabolismMaría-José de Castro, Paula Sánchez-Pintos, Nisreem Abdelaziz-Salem, et al.
Molecular Genetics and Metabolism|June 8, 2013
A glimpse into past, present, and future DNA sequencingMarcos Morey, Ana Fernández-Marmiesse, Daisy Castiñeiras, et al.
Nutrients|December 16, 2020
Metabolic Bone Disease of Prematurity: Risk Factors and Associated Short-Term OutcomesAlejandro Avila-Alvarez, Adela Urisarri, Jesús Fuentes-Carballal, et al.
International Journal of Molecular Sciences|December 11, 2022
Proteomics in Inherited Metabolic DisordersMaria Del Pilar Chantada-Vázquez, Susana B Bravo, Sofía Barbosa-Gouveia, et al.
Medicine|July 20, 2018
Diagnosis and follow-up of patients with Hunter syndrome in Spain: A Delphi consensusLuis González-Gutiérrez-Solana, Encarnación Guillén-Navarro, Mireia Del Toro, et al.
Medicina Clinica|February 25, 2014
[Utility of bone turnover markers in metabolic bone disease detection in patients with phenylketonuria]Alicia Mirás, Antonio Freire Corbacho, Javier Rodríguez García, et al.
Medicine|April 16, 2019
Acylcarnitine profile in neonatal hypoxic-ischemic encephalopathy: The value of butyrylcarnitine as a prognostic markerOlalla López-Suárez, Ana Concheiro-Guisán, Paula Sánchez-Pintos, et al.
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