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L Beaulieu

Showing results (111-120 of 187) with videos related to

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Epilepsia|June 7, 2014
Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutationSunita Venkateswaran, Ken A Myers, Amanda C Smith, et al.
International Journal of Medical Informatics|April 23, 2026
Decision support systems (DSS) for predicting hypertensive events using real-world telemonitoring dataHye-Chung Kum, Carl W Tong, Suhu Lavu, et al.
Journal of the American Chemical Society|October 15, 2010
Importance of ligand bioactive conformation in the discovery of potent indole-diamide inhibitors of the hepatitis C virus NS5BSteven R LaPlante, James R Gillard, Araz Jakalian, et al.
BMC Medical Genetics|March 28, 2014
Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial diseaseHugh J McMillan, Jeremy Schwartzentruber, Amanda Smith, et al.
American Journal of Medical Genetics. Part A|September 28, 2016
A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite populationRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
Journal of Child Neurology|October 22, 2014
Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl-Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations: The Expanding Phenotype of Aminoacyl-Transfer RNA Synthetase Mutations in Human DiseaseHugh J McMillan, Peter Humphreys, Amanda Smith, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Response to correspondence of NDUFS4-related Leigh syndrome in HutteritesRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
SSM - Population Health|May 19, 2025
The contribution of social determinants of health to long-term outcomes following traumatic brain injuryJohn D Corrigan, Mike Vuolo, Rebecca Shankman, et al.
Neurobiology of Aging|October 16, 2014
Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathologyDavid A Dyment, Amanda C Smith, Peter Humphreys, et al.
The American Journal of Sports Medicine|July 14, 2021
The Anterior Cruciate Ligament Can Become Hypertrophied in Response to Mechanical Loading: A Magnetic Resonance Imaging Study in Elite AthletesMélanie L Beaulieu, Madeleine G DeClercq, Nathan T Rietberg, et al.
Pageof 19

Showing results (111-120 of 187) with videos related to

Sort By:
Pageof 19
Epilepsia|June 7, 2014
Whole-exome sequencing in an individual with severe global developmental delay and intractable epilepsy identifies a novel, de novo GRIN2A mutationSunita Venkateswaran, Ken A Myers, Amanda C Smith, et al.
International Journal of Medical Informatics|April 23, 2026
Decision support systems (DSS) for predicting hypertensive events using real-world telemonitoring dataHye-Chung Kum, Carl W Tong, Suhu Lavu, et al.
Journal of the American Chemical Society|October 15, 2010
Importance of ligand bioactive conformation in the discovery of potent indole-diamide inhibitors of the hepatitis C virus NS5BSteven R LaPlante, James R Gillard, Araz Jakalian, et al.
BMC Medical Genetics|March 28, 2014
Compound heterozygous mutations in glycyl-tRNA synthetase are a proposed cause of systemic mitochondrial diseaseHugh J McMillan, Jeremy Schwartzentruber, Amanda Smith, et al.
American Journal of Medical Genetics. Part A|September 28, 2016
A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite populationRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
Journal of Child Neurology|October 22, 2014
Congenital Visual Impairment and Progressive Microcephaly Due to Lysyl-Transfer Ribonucleic Acid (RNA) Synthetase (KARS) Mutations: The Expanding Phenotype of Aminoacyl-Transfer RNA Synthetase Mutations in Human DiseaseHugh J McMillan, Peter Humphreys, Amanda Smith, et al.
American Journal of Medical Genetics. Part A|April 4, 2017
Response to correspondence of NDUFS4-related Leigh syndrome in HutteritesRyan E Lamont, Chandree L Beaulieu, Francois P Bernier, et al.
SSM - Population Health|May 19, 2025
The contribution of social determinants of health to long-term outcomes following traumatic brain injuryJohn D Corrigan, Mike Vuolo, Rebecca Shankman, et al.
Neurobiology of Aging|October 16, 2014
Homozygous nonsense mutation in SYNJ1 associated with intractable epilepsy and tau pathologyDavid A Dyment, Amanda C Smith, Peter Humphreys, et al.
The American Journal of Sports Medicine|July 14, 2021
The Anterior Cruciate Ligament Can Become Hypertrophied in Response to Mechanical Loading: A Magnetic Resonance Imaging Study in Elite AthletesMélanie L Beaulieu, Madeleine G DeClercq, Nathan T Rietberg, et al.
Pageof 19