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Isabelle Desguerre

Showing results (101-110 of 235) with videos related to

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American Journal of Human Genetics|March 6, 2008
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizuresJulie Mollet, Agnès Delahodde, Valérie Serre, et al.
Frontiers in Neurology|March 14, 2022
The Use and Outcomes of Motor Rehabilitation Services Among People With Cerebral Palsy Change Across the LifespanGwenaël Cornec, Sylvain Brochard, Gaelle Drewnowski, et al.
Cerebral Cortex (New York, N.Y. : 1991)|December 1, 2023
Identifying interindividual variability of social perception and associated brain anatomical correlations in children with autism spectrum disorder using eye-tracking and diffusion tensor imaging MRI (DTI-MRI)Alice Vinçon-Leite, Ana Saitovitch, Herve Lemaître, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Diaphragmatic dysfunction in SEPN1-related myopathySerena Caggiano, Sonia Khirani, Ivana Dabaj, et al.
European Journal of Human Genetics : EJHG|July 9, 2015
A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophyLam Son Nguyen, Taiane Schneider, Marlène Rio, et al.
European Journal of Human Genetics : EJHG|September 6, 2012
Expanding the spectrum of TUBA1A-related cortical dysgenesis to PolymicrogyriaKarine Poirier, Yoann Saillour, Franck Fourniol, et al.
Neuromuscular Disorders : NMD|July 14, 2020
Evidence of diaphragmatic dysfunction with severe alveolar hypoventilation syndrome in mitochondrial respiratory chain deficiencyGiulia Barcia, Sonia Khirani, Alessandro Amaddeo, et al.
Archives of Orthopaedic and Trauma Surgery|December 19, 2022
Perioperative complications after posterior spinal fusion versus minimally invasive fusionless surgery in neuromuscular scoliosis: a comparative studyMathilde Gaume, Josiane Njiki, Isabelle Vaugier, et al.
Neurogenetics|October 12, 2016
Mosaicism in ATP1A3-related disorders: not just a theoretical riskMarie Hully, Juliette Ropars, Laurence Hubert, et al.
Journal of Cell Science|May 9, 2014
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursorsAnne T Bertrand, Simindokht Ziaei, Camille Ehret, et al.
Pageof 24

Showing results (101-110 of 235) with videos related to

Sort By:
Pageof 24
American Journal of Human Genetics|March 6, 2008
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizuresJulie Mollet, Agnès Delahodde, Valérie Serre, et al.
Frontiers in Neurology|March 14, 2022
The Use and Outcomes of Motor Rehabilitation Services Among People With Cerebral Palsy Change Across the LifespanGwenaël Cornec, Sylvain Brochard, Gaelle Drewnowski, et al.
Cerebral Cortex (New York, N.Y. : 1991)|December 1, 2023
Identifying interindividual variability of social perception and associated brain anatomical correlations in children with autism spectrum disorder using eye-tracking and diffusion tensor imaging MRI (DTI-MRI)Alice Vinçon-Leite, Ana Saitovitch, Herve Lemaître, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Diaphragmatic dysfunction in SEPN1-related myopathySerena Caggiano, Sonia Khirani, Ivana Dabaj, et al.
European Journal of Human Genetics : EJHG|July 9, 2015
A nonsense variant in HERC1 is associated with intellectual disability, megalencephaly, thick corpus callosum and cerebellar atrophyLam Son Nguyen, Taiane Schneider, Marlène Rio, et al.
European Journal of Human Genetics : EJHG|September 6, 2012
Expanding the spectrum of TUBA1A-related cortical dysgenesis to PolymicrogyriaKarine Poirier, Yoann Saillour, Franck Fourniol, et al.
Neuromuscular Disorders : NMD|July 14, 2020
Evidence of diaphragmatic dysfunction with severe alveolar hypoventilation syndrome in mitochondrial respiratory chain deficiencyGiulia Barcia, Sonia Khirani, Alessandro Amaddeo, et al.
Archives of Orthopaedic and Trauma Surgery|December 19, 2022
Perioperative complications after posterior spinal fusion versus minimally invasive fusionless surgery in neuromuscular scoliosis: a comparative studyMathilde Gaume, Josiane Njiki, Isabelle Vaugier, et al.
Neurogenetics|October 12, 2016
Mosaicism in ATP1A3-related disorders: not just a theoretical riskMarie Hully, Juliette Ropars, Laurence Hubert, et al.
Journal of Cell Science|May 9, 2014
Cellular microenvironments reveal defective mechanosensing responses and elevated YAP signaling in LMNA-mutated muscle precursorsAnne T Bertrand, Simindokht Ziaei, Camille Ehret, et al.
Pageof 24