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Revista Portuguesa De Cardiologia : Orgao Oficial Da Sociedade Portuguesa De Cardiologia = Portuguese Journal of Cardiology : an Official Journal of the Portuguese Society of Cardiology|September 16, 2023
Home- versus centre-based EXercise InTervention in patients with Heart Failure (EXIT-HF trial): A pragmatic randomized controlled trialCristine Schmidt, Sandra Magalhães, Priscilla Gois Basilio, et al.Biochimica Et Biophysica Acta|July 16, 2013
Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficientSara Violante, Lodewijk Ijlst, Heleen Te Brinke, et al.Transplantation Proceedings|January 9, 2021
Viral Clearance and Serological Response to SARS-CoV-2 in Kidney Transplant RecipientsJosé Silvano, Filipa Ferreira, Manuela Bustorff, et al.Journal of Hepatology|December 15, 2010
New insights on the mechanisms of valproate-induced hyperammonemia: inhibition of hepatic N-acetylglutamate synthase activity by valproyl-CoACátia C P Aires, Arno van Cruchten, Lodewijk Ijlst, et al.Endocrine, Metabolic & Immune Disorders Drug Targets|September 15, 2023
Glutaric Acidemia Type 1: Diagnosis, Clinical features, and Outcome in a Portuguese CohortPatrícia Lipari Pinto, Beatriz Câmara, Cristina Florindo, et al.Biochimie|February 15, 2021
Structural and functional impact of clinically relevant E1α variants causing pyruvate dehydrogenase complex deficiencyHana Pavlu-Pereira, Diana Lousa, Catarina S Tomé, et al.Biochemical Pharmacology|October 27, 2009
Inhibition of hepatic carnitine palmitoyl-transferase I (CPT IA) by valproyl-CoA as a possible mechanism of valproate-induced steatosisCátia C P Aires, Lodewijk Ijlst, Femke Stet, et al.Nefrologia|August 31, 2024
Familial juvenile hyperuricemic nephropathy: Revisiting the SLC8A1 gene, in a family with a novel terminal gross deletion in the UMOD geneFrancisco Gonçalves, Pedro Lisboa-Gonçalves, Rita Quental, et al.Clinical Chemistry|July 26, 2003
Increased homocysteine and S-adenosylhomocysteine concentrations and DNA hypomethylation in vascular diseaseRita Castro, Isabel Rivera, Eduard A Struys, et al.European Journal of Human Genetics : EJHG|July 24, 2014
Functional correction by antisense therapy of a splicing mutation in the GALT geneAna I Coelho, Sílvia Lourenço, Matilde Trabuco, et al.Pageof 12