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P RICHARD

Showing results (911-920 of 939) with videos related to

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Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Plos One|April 18, 2015
Absolute leukocyte telomere length in HIV-infected and uninfected individuals: evidence of accelerated cell senescence in HIV-associated chronic obstructive pulmonary diseaseJoseph C Y Liu, Janice M Leung, David A Ngan, et al.
Annales De Cardiologie Et D'Angeiologie|November 9, 2015
[Characteristics and management of ST-elevation myocardial infarction in France: Regional variations in 2010]A Sokoloff, G Lefèvre, N Teixeira, et al.
Journal of Virology|November 13, 2015
Population-Level Immune-Mediated Adaptation in HIV-1 Polymerase during the North American EpidemicNatalie N Kinloch, Daniel R MacMillan, Anh Q Le, et al.
Plos One|August 20, 2009
HLA-associated immune escape pathways in HIV-1 subtype B Gag, Pol and Nef proteinsZabrina L Brumme, Mina John, Jonathan M Carlson, et al.
Journal of Clinical Microbiology|January 31, 2014
Comparative performances of HIV-1 RNA load assays at low viral load levels: results of an international collaborationLuke C Swenson, Bryan Cobb, Anna Maria Geretti, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
AIDS (London, England)|August 24, 2017
Prevalence and clinical impacts of HIV-1 intersubtype recombinants in Uganda revealed by near-full-genome population and deep sequencing approachesGuinevere Q Lee, David R Bangsberg, Theresa Mo, et al.
Pageof 94

Showing results (911-920 of 939) with videos related to

Sort By:
Pageof 94
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Plos One|April 18, 2015
Absolute leukocyte telomere length in HIV-infected and uninfected individuals: evidence of accelerated cell senescence in HIV-associated chronic obstructive pulmonary diseaseJoseph C Y Liu, Janice M Leung, David A Ngan, et al.
Annales De Cardiologie Et D'Angeiologie|November 9, 2015
[Characteristics and management of ST-elevation myocardial infarction in France: Regional variations in 2010]A Sokoloff, G Lefèvre, N Teixeira, et al.
Journal of Virology|November 13, 2015
Population-Level Immune-Mediated Adaptation in HIV-1 Polymerase during the North American EpidemicNatalie N Kinloch, Daniel R MacMillan, Anh Q Le, et al.
Plos One|August 20, 2009
HLA-associated immune escape pathways in HIV-1 subtype B Gag, Pol and Nef proteinsZabrina L Brumme, Mina John, Jonathan M Carlson, et al.
Journal of Clinical Microbiology|January 31, 2014
Comparative performances of HIV-1 RNA load assays at low viral load levels: results of an international collaborationLuke C Swenson, Bryan Cobb, Anna Maria Geretti, et al.
Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.
Revue Neurologique|September 17, 2016
Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNCD Avila-Smirnow, L Gueneau, S Batonnet-Pichon, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
AIDS (London, England)|August 24, 2017
Prevalence and clinical impacts of HIV-1 intersubtype recombinants in Uganda revealed by near-full-genome population and deep sequencing approachesGuinevere Q Lee, David R Bangsberg, Theresa Mo, et al.
Pageof 94