Zobrazeno 1 - 10
of 161
pro vyhledávání: '"Fátima Leal"'
Autor:
Fátima Leal, Micaela Pinho
Publikováno v:
Administrative Sciences, Vol 14, Iss 6, p 128 (2024)
Despite much research being conducted within the scope of sustainable tourism, more progress has yet to be made in defining how close or far different countries are from achieving this goal. Consequently, this paper aims to evaluate and compare the c
Externí odkaz:
https://doaj.org/article/b3b7ebcdcf9c4b6ba2565253a1564e8d
Autor:
Fátima Leal
Publikováno v:
Ensaio, Vol 31, Iss 119, Pp 332-353 (2023)
Este estudo pretende identificar as estratégias de estudo e de aprendizagem utilizadas por estudantes de Ensino Superior. Participaram 48 jovens adultos voluntários, homens e mulheres, estudantes do primeiro e do terceiro anos de cursos de licencia
Externí odkaz:
https://doaj.org/article/15d36e15a91b4a76807a3a6a90a7c9a8
Autor:
Alejandro Soriano-Sexto, Diana Gallego, Fátima Leal, Natalia Castejón-Fernández, Rosa Navarrete, Patricia Alcaide, María L. Couce, Elena Martín-Hernández, Pilar Quijada-Fraile, Luis Peña-Quintana, Raquel Yahyaoui, Patricia Correcher, Magdalena Ugarte, Pilar Rodríguez-Pombo, Belén Pérez
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 21, p 12850 (2022)
Inborn errors of metabolism (IEM) constitute a huge group of rare diseases affecting 1 in every 1000 newborns. Next-generation sequencing has transformed the diagnosis of IEM, leading to its proposed use as a second-tier technology for confirming cas
Externí odkaz:
https://doaj.org/article/a172615f1c064b6fbb45301c2321c57c
Autor:
Sandra Brasil, Fátima Leal, Ana Vega, Rosa Navarrete, María Jesús Ecay, Lourdes R. Desviat, Casandra Riera, Natàlia Padilla, Xavier de la Cruz, Mari Luz Couce, Elena Martin-Hernández, Ana Morais, Consuelo Pedrón, Luis Peña-Quintana, Miriam Rigoldi, Norma Specola, Isabel Tavares de Almeida, Inmaculada Vives, Raquel Yahyaoui, Pilar Rodríguez-Pombo, Magdalena Ugarte, Celia Pérez-Cerda, Begoña Merinero, Belén Pérez
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-12 (2018)
Abstract Background Cellular cobalamin defects are a locus and allelic heterogeneous disorder. The gold standard for coming to genetic diagnoses of cobalamin defects has for some time been gene-by-gene Sanger sequencing of individual DNA fragments. E
Externí odkaz:
https://doaj.org/article/1e43991c7efe4b65b577dbeda655da5f
Publikováno v:
Data Science and Engineering, Vol 2, Iss 3, Pp 199-209 (2017)
Abstract As a recommendation technique based on historical user information, collaborative filtering typically predicts the classification of items using a single criterion for a given user. However, many application domains can benefit from the anal
Externí odkaz:
https://doaj.org/article/016678d7ab2940e3a82e6bb9b5d9437f
Autor:
Eva Richard PhD, Sandra Brasil PhD, Fátima Leal, Rosa Navarrete, Ana Vega PhD, María Jesús Ecay, Lourdes R. Desviat PhD, Celia Pérez-Cerda PhD, Magdalena Ugarte PhD, Begoña Merinero PhD, Belén Pérez PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 5 (2017)
Genetic defects affecting the remethylation pathway cause hyperhomocysteinemia. Isolated remethylation defects are caused by mutations of the 5, 10-methylenetetrahydrofolate reductase (MTHFR) , methionine synthase reductase (MTRR) , methionine syntha
Externí odkaz:
https://doaj.org/article/44f70f4286a0470fa48d2a3b2284befa
Autor:
Fátima Leal
Publikováno v:
Revista Portuguesa de Medicina Geral e Familiar, Vol 19, Iss 1 (2003)
A transmissão de más notícias é encarada com alguma dificuldade por parte da maioria dos profissionais de saúde pela complexidade dos aspectos emotivos que lhe estão associados. Por outro lado, a preparação nesta área também é deficitária
Externí odkaz:
https://doaj.org/article/61d299656cc74313bb1e177a80d1d494
Autor:
Obdulia Sánchez‐Lijarcio, Delia Yubero, Fátima Leal, María L. Couce, Luis González Gutiérrez‐Solana, Eduardo López‐Laso, Àngels García‐Cazorla, Leticia Pías‐Peleteiro, Begoña de Azua Brea, Salvador Ibáñez‐Micó, Gonzalo Mateo‐Martínez, Monica Troncoso‐Schifferli, Scarlet Witting‐Enriquez, Magdalena Ugarte, Rafael Artuch, Belén Pérez
Publikováno v:
Biblos-e Archivo. Repositorio Institucional de la UAM
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Glucose transporter 1 deficiency syndrome (GLUT1DS) is a neurometabolic disorder caused by haploinsufficiency of the GLUT1 glucose transporter (encoded by SLC2A1) leading to defective glucose transport across the blood–brain barrier. This work desc
Autor:
Fátima Leal
Publikováno v:
Ensaio: Avaliação e Políticas Públicas em Educação, Volume: 31, Issue: 119, Article number: e0233349, Published: 17 APR 2023
Resumo Este estudo pretende identificar as estratégias de estudo e de aprendizagem utilizadas por estudantes de Ensino Superior. Participaram 48 jovens adultos voluntários, homens e mulheres, estudantes do primeiro e do terceiro anos de cursos de l