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Journal of Inherited Metabolic Disease|December 15, 2016
Small molecules as therapeutic agents for inborn errors of metabolismLeslie Matalonga, Laura Gort, Antonia RibesMolecular Genetics and Metabolism|July 6, 2004
Guanidinoacetate and creatine/creatinine levels in controls and patients with urea cycle defectsAngela Arias, Judit Garcia-Villoria, Antonia RibesJournal of Inherited Metabolic Disease|September 3, 2016
Differential diagnosis of lipoic acid synthesis defectsFrederic Tort, Xènia Ferrer-Cortes, Antonia RibesPediatric Neurology|April 18, 2007
Neuroimage findings in 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiencyMaría R Cazorla, Alfonso Verdú, Celia Pérez-Cerdá, et al.Clinical Biochemistry|October 20, 2012
Improvement of the cystine measurement in granulocytes by liquid chromatograhy-tandem mass spectrometryJudit García-Villoria, Jose Maria Hernández-Pérez, Angela Arias, et al.Molecular Genetics and Metabolism|January 15, 2013
Role of creatine as biomarker of mitochondrial diseasesSonia Pajares, Angela Arias, Judit García-Villoria, et al.Journal of Inherited Metabolic Disease|April 30, 2014
Lipoic acid biosynthesis defectsJohannes A Mayr, René G Feichtinger, Frederic Tort, et al.Seminars in Pediatric Neurology|March 13, 2017
Neonatal Screening for Inherited Metabolic Diseases in 2016Judit Garcia Villoria, Sonia Pajares, Rosa María López, et al.Journal of Inherited Metabolic Disease|December 19, 2013
Treatment effect of coenzyme Q(10) and an antioxidant cocktail in fibroblasts of patients with Sanfilippo diseaseLeslie Matalonga, Angela Arias, María Josep Coll, et al.American Journal of Obstetrics and Gynecology|April 21, 2009
Predictive value of combined amniotic fluid proteomic biomarkers and interleukin-6 in preterm labor with intact membranesTeresa Cobo, Montse Palacio, Aleix Navarro-Sastre, et al.Pageof 11