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J H Smith

Showing results (561-570 of 588) with videos related to

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Anaesthesia|November 16, 2023
Peri-operative cardiac arrest: epidemiology and clinical features of patients analysed in the 7th National Audit Project of the Royal College of AnaesthetistsR A Armstrong, J Soar, A D Kane, et al.
European Journal of Human Genetics : EJHG|January 5, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, et al.
Journal of Medical Genetics|October 9, 2015
Characterising the spectrum of autosomal recessive hereditary hearing loss in IranChristina M Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian, et al.
Anaesthesia|November 16, 2023
Peri-operative cardiac arrest: management and outcomes of patients analysed in the 7th National Audit Project of the Royal College of AnaesthetistsR A Armstrong, T M Cook, A D Kane, et al.
Journal of Medical Genetics|May 20, 2015
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorderLiang Zong, Jing Guan, Megan Ealy, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Monoclonal nephritic factors reveal insights into C3 convertase dynamics and dysregulationSeth J Welsh, Christopher T Culek, Zhen Xu, et al.
Anaesthesia|November 3, 2023
The 7th National Audit Project (NAP7) baseline survey of individual anaesthetists: preparedness for and experiences of peri-operative cardiac arrestE Kursumovic, T M Cook, D N Lucas, et al.
International Journal of Pediatric Otorhinolaryngology|August 21, 2022
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Evaluation and management of congenital tracheal stenosisDouglas R Sidell, Kara D Meister, Alessandro de Alarcon, et al.
American Journal of Human Genetics|October 23, 2003
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationGregory S Hageman, Don H Anderson, Lincoln V Johnson, et al.
Pageof 59

Showing results (561-570 of 588) with videos related to

Sort By:
Pageof 59
Anaesthesia|November 16, 2023
Peri-operative cardiac arrest: epidemiology and clinical features of patients analysed in the 7th National Audit Project of the Royal College of AnaesthetistsR A Armstrong, J Soar, A D Kane, et al.
European Journal of Human Genetics : EJHG|January 5, 2021
A synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicingYoel Hirsch, Chayada Tangshewinsirikul, Kevin T Booth, et al.
Journal of Medical Genetics|October 9, 2015
Characterising the spectrum of autosomal recessive hereditary hearing loss in IranChristina M Sloan-Heggen, Mojgan Babanejad, Maryam Beheshtian, et al.
Anaesthesia|November 16, 2023
Peri-operative cardiac arrest: management and outcomes of patients analysed in the 7th National Audit Project of the Royal College of AnaesthetistsR A Armstrong, T M Cook, A D Kane, et al.
Journal of Medical Genetics|May 20, 2015
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorderLiang Zong, Jing Guan, Megan Ealy, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Monoclonal nephritic factors reveal insights into C3 convertase dynamics and dysregulationSeth J Welsh, Christopher T Culek, Zhen Xu, et al.
Anaesthesia|November 3, 2023
The 7th National Audit Project (NAP7) baseline survey of individual anaesthetists: preparedness for and experiences of peri-operative cardiac arrestE Kursumovic, T M Cook, D N Lucas, et al.
International Journal of Pediatric Otorhinolaryngology|August 21, 2022
International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Evaluation and management of congenital tracheal stenosisDouglas R Sidell, Kara D Meister, Alessandro de Alarcon, et al.
American Journal of Human Genetics|October 23, 2003
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter studyIgnacio Del Castillo, Miguel A Moreno-Pelayo, Francisco J Del Castillo, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 5, 2005
A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degenerationGregory S Hageman, Don H Anderson, Lincoln V Johnson, et al.
Pageof 59