Search Results - Delia Yubero

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  1. 1

    Targeted Next Generation Sequencing in Patients with Inborn Errors of Metabolism. by Dèlia Yubero, Núria Brandi, Aida Ormazabal, Àngels Garcia-Cazorla, Belén Pérez-Dueñas, Jaime Campistol, Antonia Ribes, Francesc Palau, Rafael Artuch, Judith Armstrong, Working Group

    Published in PLoS ONE (2016-01-01)
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  2. 2

    Coenzyme Q in the Treatment of Mitochondrial Disease by Viruna Neergheen MSc, Annapurna Chalasani MSc, Luke Wainwright MSci, MRes, Delia Yubero PhD, Raquel Montero PhD, Rafael Artuch MD, PhD, Iain Hargreaves PhD

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  3. 3

    Exploring Plasma Coenzyme Q<sub>10</sub> Status in Paediatric Dyslipidaemia by Beatriz Minguez, Mariela de Los Santos, Camila Garcia-Volpe, Cristina Molera, Abraham J. Paredes-Fuentes, Clara Oliva, Angela Arias, Helena Rodriguez-Gonzalez, Delia Yubero, Mireia Tondo, Carlos Santos-Ocaña, Silvia Meavilla, Rafael Artuch

    Published in Antioxidants (2024-08-01)
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  4. 4

    Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum by Florencia Pérez‐Vidarte, Berta Estévez‐Arias, Leslie Matalonga, Delia Yubero, Anna Codina, Carlos Ortez, Julita Medina, Lidia DeSena DeCabo, Laura Carrera‐García, Jesica Expósito‐Escudero, Cristina Jou, Eduardo F. Tizzano, Andres Nascimento, Daniel Natera‐de Benito

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  5. 5

    Molecular Characterization of New FBXL4 Mutations in Patients With mtDNA Depletion Syndrome by Sonia Emperador, Sonia Emperador, Sonia Emperador, Nuria Garrido-Pérez, Nuria Garrido-Pérez, Nuria Garrido-Pérez, Javier Amezcua-Gil, Paula Gaudó, Julio Alberto Andrés-Sanz, Delia Yubero, Delia Yubero, Ana Fernández-Marmiesse, Maria M. O’Callaghan, Maria M. O’Callaghan, Juan D. Ortigoza-Escobar, Juan D. Ortigoza-Escobar, Marti Iriondo, Marti Iriondo, Eduardo Ruiz-Pesini, Eduardo Ruiz-Pesini, Eduardo Ruiz-Pesini, Eduardo Ruiz-Pesini, Angels García-Cazorla, Angels García-Cazorla, Mercedes Gil-Campos, Mercedes Gil-Campos, Rafael Artuch, Rafael Artuch, Julio Montoya, Julio Montoya, Julio Montoya, María Pilar Bayona-Bafaluy, María Pilar Bayona-Bafaluy, María Pilar Bayona-Bafaluy

    Published in Frontiers in Genetics (2020-01-01)
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  6. 6

    GDF-15 Is Elevated in Children with Mitochondrial Diseases and Is Induced by Mitochondrial Dysfunction. by Raquel Montero, Delia Yubero, Joan Villarroya, Desiree Henares, Cristina Jou, Maria Angeles Rodríguez, Federico Ramos, Andrés Nascimento, Carlos Ignacio Ortez, Jaume Campistol, Belen Perez-Dueñas, Mar O'Callaghan, Mercedes Pineda, Angeles Garcia-Cazorla, Jaume Colomer Oferil, Julio Montoya, Eduardo Ruiz-Pesini, Sonia Emperador, Marija Meznaric, Laura Campderros, Susana G Kalko, Francesc Villarroya, Rafael Artuch, Cecilia Jimenez-Mallebrera

    Published in PLoS ONE (2016-01-01)
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  7. 7

    Erratum to: Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders by Linda Cassis, Elisenda Cortès-Saladelafont, Marta Molero-Luis, Delia Yubero, Maria Julieta González, Aida Ormazábal, Carme Fons, Cristina Jou, Cristina Sierra, Esperanza Castejon Ponce, Federico Ramos, Judith Armstrong, M. Mar O’Callaghan, Mercedes Casado, Raquel Montero, Silvia Meavilla-Olivas, Rafael Artuch, Ivo Barić, Franco Bartoloni, Cinzia Maria Bellettato, Fedele Bonifazi, Adriana Ceci, Ljerka Cvitanović-Šojat, Christine I. Dali, Francesca D’Avanzo, Ksenija Fumic, Viviana Giannuzzi, Christina Lampe, Maurizio Scarpa, Ángels Garcia-Cazorla

    Published in Orphanet Journal of Rare Diseases (2016-11-01)
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