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J Coll

Showing results (331-340 of 344) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 16, 1998
A dysfunctional desmin mutation in a patient with severe generalized myopathyA M Muñoz-Mármol, G Strasser, M Isamat, et al.
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 <i>In Vivo</i> 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.
Pageof 35

Showing results (331-340 of 344) with videos related to

Sort By:
Pageof 35
Proceedings of the National Academy of Sciences of the United States of America|September 16, 1998
A dysfunctional desmin mutation in a patient with severe generalized myopathyA M Muñoz-Mármol, G Strasser, M Isamat, et al.
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 <i>In Vivo</i> 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.
Pageof 35