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Showing results (371-380 of 380) with videos related to

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Eneuro|October 20, 2015
CSF and Blood Levels of GFAP in Alexander DiseasePaige L Jany, Guillermo E Agosta, William S Benko, et al.
Journal of Dairy Science|June 30, 2026
Assessing implementation of biosecurity practices in Canadian dairy farms: An observational studyVitoria R Lima-Campêlo, Mariana Fonseca, Marie-Pascale Morin, et al.
Neurology. Genetics|June 26, 2020
Expanding the phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophyStefanie Perrier, Laurence Gauquelin, Catherine Fallet-Bianco, et al.
Preventive Veterinary Medicine|October 16, 2025
Automating classification of veterinary biosecurity recommendations using machine learningVitória R Lima-Campêlo, Mariana Fonseca, Marie-Pascale Morin, et al.
HGG Advances|July 20, 2025
Comprehensive genotype-phenotype analysis in POLR3-related disordersMackenzie A Michell-Robinson, Stefanie Perrier, Samuel Gauthier, et al.
Plos One|November 20, 2024
Treatment approaches to horses with acute diarrhea admitted to referral institutions: A multicenter retrospective studyDiego E Gomez, Jamie J Kopper, David P Byrne, et al.
Molecular Genetics and Metabolism|September 3, 2017
Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophiesLaura A Adang, Omar Sherbini, Laura Ball, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2021
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafishSheng-Jia Lin, Barbara Vona, Patricia G Barbalho, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3Schaida Schirwani, Shadi Albaba, Deanna Alexis Carere, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.
Pageof 38

Showing results (371-380 of 380) with videos related to

Sort By:
Pageof 38
You have reached the last page of results.This site can display upto 380 results.
Eneuro|October 20, 2015
CSF and Blood Levels of GFAP in Alexander DiseasePaige L Jany, Guillermo E Agosta, William S Benko, et al.
Journal of Dairy Science|June 30, 2026
Assessing implementation of biosecurity practices in Canadian dairy farms: An observational studyVitoria R Lima-Campêlo, Mariana Fonseca, Marie-Pascale Morin, et al.
Neurology. Genetics|June 26, 2020
Expanding the phenotypic and molecular spectrum of RNA polymerase III-related leukodystrophyStefanie Perrier, Laurence Gauquelin, Catherine Fallet-Bianco, et al.
Preventive Veterinary Medicine|October 16, 2025
Automating classification of veterinary biosecurity recommendations using machine learningVitória R Lima-Campêlo, Mariana Fonseca, Marie-Pascale Morin, et al.
HGG Advances|July 20, 2025
Comprehensive genotype-phenotype analysis in POLR3-related disordersMackenzie A Michell-Robinson, Stefanie Perrier, Samuel Gauthier, et al.
Plos One|November 20, 2024
Treatment approaches to horses with acute diarrhea admitted to referral institutions: A multicenter retrospective studyDiego E Gomez, Jamie J Kopper, David P Byrne, et al.
Molecular Genetics and Metabolism|September 3, 2017
Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophiesLaura A Adang, Omar Sherbini, Laura Ball, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 26, 2021
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafishSheng-Jia Lin, Barbara Vona, Patricia G Barbalho, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Expanding the phenotype of ASXL3-related syndrome: A comprehensive description of 45 unpublished individuals with inherited and de novo pathogenic variants in ASXL3Schaida Schirwani, Shadi Albaba, Deanna Alexis Carere, et al.
European Journal of Human Genetics : EJHG|June 3, 2020
A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndromeTheodore G Drivas, Dong Li, Divya Nair, et al.
Pageof 38