Showing results (191-200 of 203) with videos related to
Sort By:
Pageof 21
Revista De Neurologia|December 29, 2000
[Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA]L Coelho-Miranda, A Playan, R Artuch, et al.Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|August 28, 2017
Early detection of HIV infection and of asymptomatic sexually transmitted infections among men who have sex with menJ Coll, S Videla, A Leon, et al.Thrombosis Update|April 15, 2024
Vaccine-induced thrombosis and thrombocytopenia (VITT) in Ireland: A review of cases and current practicesD Swan, H Enright, R Desmond, et al.Journal of Virology|June 9, 2017
Identification of Interleukin-27 (IL-27)/IL-27 Receptor Subunit Alpha as a Critical Immune Axis for In Vivo HIV ControlM Ruiz-Riol, D Berdnik, A Llano, et al.Marine Pollution Bulletin|May 31, 2001
ENCORE: the effect of nutrient enrichment on coral reefs. Synthesis of results and conclusionsK Koop, D Booth, A Broadbent, et al.Journal of Medical Genetics|June 1, 1996
Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: new mutations and the paradox between genotype and phenotypeJ L Keulemans, A J Reuser, M A Kroos, et al.Pediatric Research|August 29, 2000
Glutaryl-CoA dehydrogenase deficiency in Spain: evidence of two groups of patients, genetically, and biochemically distinctC Busquets, B Merinero, E Christensen, et al.Molecular Genetics and Metabolism|January 9, 2010
Clinical experience with miglustat therapy in pediatric patients with Niemann-Pick disease type C: a case seriesM Pineda, M S Perez-Poyato, M O'Callaghan, et al.Molecular Genetics and Metabolism|April 15, 2014
Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutationsA Morrone, K L Tylee, M Al-Sayed, et al.Orphanet Journal of Rare Diseases|April 8, 2018
Consensus clinical management guidelines for Niemann-Pick disease type CTarekegn Geberhiwot, Alessandro Moro, Andrea Dardis, et al.Pageof 21