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J H Smith

Showing results (541-550 of 588) with videos related to

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Human Molecular Genetics|May 9, 2015
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxiaJohn A Damiano, Zaid Afawi, Melanie Bahlo, et al.
Kidney International|June 25, 2022
Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathySophie Chauvet, Jill J Hauer, Florent Petitprez, et al.
Journal of the American Society of Nephrology : JASN|April 1, 2005
Membranoproliferative glomerulonephritis type II (dense deposit disease): an updateGerald B Appel, H Terence Cook, Gregory Hageman, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
Journal of Medical Genetics|June 28, 2013
Advancing genetic testing for deafness with genomic technologyA Eliot Shearer, E Ann Black-Ziegelbein, Michael S Hildebrand, et al.
International Journal of Pediatric Otorhinolaryngology|September 6, 2020
International Pediatric Otolaryngology Group (IPOG): Consensus recommendations on the prenatal and perinatal management of anticipated airway obstructionMichael D Puricelli, Reza Rahbar, Gregory C Allen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 19, 2019
International Pediatric Otolaryngology Group (IPOG) Consensus Recommendations: Congenital CholesteatomaFrançoise Denoyelle, François Simon, Kay W Chang, et al.
International Journal of Pediatric Otorhinolaryngology|April 25, 2016
International Pediatric ORL Group (IPOG) laryngomalacia consensus recommendationsJohn Carter, Reza Rahbar, Matthew Brigger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Pageof 59

Showing results (541-550 of 588) with videos related to

Sort By:
Pageof 59
Human Molecular Genetics|May 9, 2015
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxiaJohn A Damiano, Zaid Afawi, Melanie Bahlo, et al.
Kidney International|June 25, 2022
Results from a nationwide retrospective cohort measure the impact of C3 and soluble C5b-9 levels on kidney outcomes in C3 glomerulopathySophie Chauvet, Jill J Hauer, Florent Petitprez, et al.
Journal of the American Society of Nephrology : JASN|April 1, 2005
Membranoproliferative glomerulonephritis type II (dense deposit disease): an updateGerald B Appel, H Terence Cook, Gregory Hageman, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
Journal of Medical Genetics|June 28, 2013
Advancing genetic testing for deafness with genomic technologyA Eliot Shearer, E Ann Black-Ziegelbein, Michael S Hildebrand, et al.
International Journal of Pediatric Otorhinolaryngology|September 6, 2020
International Pediatric Otolaryngology Group (IPOG): Consensus recommendations on the prenatal and perinatal management of anticipated airway obstructionMichael D Puricelli, Reza Rahbar, Gregory C Allen, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|December 19, 2019
International Pediatric Otolaryngology Group (IPOG) Consensus Recommendations: Congenital CholesteatomaFrançoise Denoyelle, François Simon, Kay W Chang, et al.
International Journal of Pediatric Otorhinolaryngology|April 25, 2016
International Pediatric ORL Group (IPOG) laryngomalacia consensus recommendationsJohn Carter, Reza Rahbar, Matthew Brigger, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 4, 2018
Statistical Validation of Rare Complement Variants Provides Insights into the Molecular Basis of Atypical Hemolytic Uremic Syndrome and C3 GlomerulopathyAmy J Osborne, Matteo Breno, Nicolo Ghiringhelli Borsa, et al.
Pageof 59