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Drug Metabolism and Personalized Therapy|February 8, 2017
Genotyping CYP2D6 by three different methods: advantages and disadvantagesCarolina Ribeiro, Patrícia Martins, Manuela GrazinaBMJ Case Reports|May 19, 2012
Neonatal liver failure due to deoxyguanosine kinase deficiencySusana Nobre, Manuela Grazina, Francisco Silva, et al.Personalized Medicine|May 18, 2018
Characterization of CYP2D6 genotypes and metabolic profiles in the Portuguese population: pharmacogenetic implicationsJosé Albuquerque, Carolina Ribeiro, Maria Eugenia G Naranjo, et al.Journal of Child Neurology|January 14, 2012
Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected associationMargarida Henriques, Luísa Diogo, Paula Garcia, et al.Pain Medicine (Malden, Mass.)|March 17, 2018
CYP2D6 Pharmacogenetics Testing and Post-Cesarean Section Pain Scores-a Preliminary StudyCarolina Ribeiro, Rosa Quinta, Ana Raposo, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 17, 2021
Identification of a novel mutation in MEF2C gene in an atypical patient with frontotemporal lobar degenerationAndreia Adrião, Isabel Santana, Carolina Ribeiro, et al.Journal of Child Neurology|April 26, 2012
Nonketotic hyperglycinemia: a cause of encephalopathy in childrenCarla Veríssimo, Paula Garcia, Marta Simões, et al.Nutricion Hospitalaria|July 2, 2013
Citrullinemia stimulation test in the evaluation of the intestinal functionBeatriz Pinto Costa, Marco Serôdio, Marta Simões, et al.European Neurology|April 30, 2005
Mitochondrial DNA variants in a portuguese population of patients with Alzheimer's diseaseManuela Grazina, Filipe Silva, Isabel Santana, et al.Neurobiology of Disease|March 10, 2004
Frontotemporal dementia and mitochondrial DNA transitionsManuela Grazina, Filipe Silva, Isabel Santana, et al.Pageof 4