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Christopher M Watson

Showing results (71-80 of 94) with videos related to

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Surgical Infections|March 23, 2018
Short-Course Antimicrobial Therapy Does Not Increase Treatment Failure Rate in Patients with Intra-Abdominal Infection Involving Fungal OrganismsNathan R Elwood, Christopher A Guidry, Therese M Duane, et al.
Surgical Infections|March 31, 2016
Obesity Is Not Associated with Antimicrobial Treatment Failure for Intra-Abdominal InfectionZachary C Dietch, Therese M Duane, Charles H Cook, et al.
Pediatrics|September 9, 2022
Benefits and Limitations of Virtual Recruitment: Perspectives From Subspeciality DirectorsTara L Petersen, Jennifer C King, Jill J Fussell, et al.
Journal of Pediatric Intensive Care|February 18, 2022
Adenoviral Respiratory Infection-Associated Mortality in Children: A Retrospective Case SeriesMichael C Spaeder, Claire Stewart, Matthew P Sharron, et al.
Human Mutation|July 31, 2025
Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target LociUmmey Hany, Christopher M Watson, Lu Liu, et al.
Journal of Medical Genetics|March 8, 2024
Biallelic variants in Plexin B2 (<i>PLXNB2</i>) cause amelogenesis imperfecta, hearing loss and intellectual disabilityClaire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 4, 2024
Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult-Onset Still's DiseaseJoanne Topping, Leon Chang, Fatima Nadat, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Journal of Medical Genetics|November 18, 2023
Heterozygous <i>COL17A1</i> variants are a frequent cause of amelogenesis imperfectaUmmey Hany, Christopher M Watson, Lu Liu, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Pageof 10

Showing results (71-80 of 94) with videos related to

Sort By:
Pageof 10
Surgical Infections|March 23, 2018
Short-Course Antimicrobial Therapy Does Not Increase Treatment Failure Rate in Patients with Intra-Abdominal Infection Involving Fungal OrganismsNathan R Elwood, Christopher A Guidry, Therese M Duane, et al.
Surgical Infections|March 31, 2016
Obesity Is Not Associated with Antimicrobial Treatment Failure for Intra-Abdominal InfectionZachary C Dietch, Therese M Duane, Charles H Cook, et al.
Pediatrics|September 9, 2022
Benefits and Limitations of Virtual Recruitment: Perspectives From Subspeciality DirectorsTara L Petersen, Jennifer C King, Jill J Fussell, et al.
Journal of Pediatric Intensive Care|February 18, 2022
Adenoviral Respiratory Infection-Associated Mortality in Children: A Retrospective Case SeriesMichael C Spaeder, Claire Stewart, Matthew P Sharron, et al.
Human Mutation|July 31, 2025
Genetic Screening of a Nonsyndromic Amelogenesis Imperfecta Patient Cohort Using a Custom smMIP Reagent for Selective Enrichment of Target LociUmmey Hany, Christopher M Watson, Lu Liu, et al.
Journal of Medical Genetics|March 8, 2024
Biallelic variants in Plexin B2 (<i>PLXNB2</i>) cause amelogenesis imperfecta, hearing loss and intellectual disabilityClaire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 4, 2024
Characterization of Genetic Landscape and Novel Inflammatory Biomarkers in Patients With Adult-Onset Still's DiseaseJoanne Topping, Leon Chang, Fatima Nadat, et al.
Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.
Journal of Medical Genetics|November 18, 2023
Heterozygous <i>COL17A1</i> variants are a frequent cause of amelogenesis imperfectaUmmey Hany, Christopher M Watson, Lu Liu, et al.
Molecular Vision|March 25, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani originZeinab Ravesh, Mohammed E El Asrag, Nicole Weisschuh, et al.
Pageof 10