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Showing results (1311-1320 of 1,344) with videos related to

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Frontiers in Neurology|November 20, 2024
Corrigendum: The predictive validity of a Brain Care Score for dementia and stroke: data from the UK Biobank cohortSanjula D Singh, Tin Oreskovic, Sinclair Carr, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Neurology|July 25, 2024
Brain Care Score and Neuroimaging Markers of Brain Health in Asymptomatic Middle-Age PersonsCyprien A Rivier, Sanjula Singh, Jasper Senff, et al.
European Journal of Neurology|May 26, 2023
Long-term follow-up of 64 children with classical infantile-onset Pompe disease since 2004: A French real-life observational studyMarine Tardieu, Céline Cudejko, Aline Cano, et al.
British Journal of Cancer|June 25, 2024
Efficacy of administration sequence: Sacituzumab Govitecan and Trastuzumab Deruxtecan in HER2-low metastatic breast cancerF Poumeaud, M Morisseau, L Cabel, et al.
Orphanet Journal of Rare Diseases|December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptomsDavid Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism|October 5, 2013
Creatine and guanidinoacetate reference values in a French populationMarie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 17, 2011
Motor and respiratory heterogeneity in Duchenne patients: implication for clinical trialsVéronique Humbertclaude, Dalil Hamroun, Kamel Bezzou, et al.
Journal of Medical Genetics|November 1, 2022
New insights into <i>CC2D2A</i>-related Joubert syndromeMadeleine Harion, Leila Qebibo, Audrey Riquet, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
Mosaic parental germline mutations causing recurrent forms of malformations of cortical developmentJulia Lauer Zillhardt, Karine Poirier, Loïc Broix, et al.
Pageof 135

Showing results (1311-1320 of 1,344) with videos related to

Sort By:
Pageof 135
Frontiers in Neurology|November 20, 2024
Corrigendum: The predictive validity of a Brain Care Score for dementia and stroke: data from the UK Biobank cohortSanjula D Singh, Tin Oreskovic, Sinclair Carr, et al.
The Journal of Allergy and Clinical Immunology|June 14, 2011
Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotypeRomain Micol, Lilia Ben Slama, Felipe Suarez, et al.
Neurology|July 25, 2024
Brain Care Score and Neuroimaging Markers of Brain Health in Asymptomatic Middle-Age PersonsCyprien A Rivier, Sanjula Singh, Jasper Senff, et al.
European Journal of Neurology|May 26, 2023
Long-term follow-up of 64 children with classical infantile-onset Pompe disease since 2004: A French real-life observational studyMarine Tardieu, Céline Cudejko, Aline Cano, et al.
British Journal of Cancer|June 25, 2024
Efficacy of administration sequence: Sacituzumab Govitecan and Trastuzumab Deruxtecan in HER2-low metastatic breast cancerF Poumeaud, M Morisseau, L Cabel, et al.
Orphanet Journal of Rare Diseases|December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptomsDavid Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism|October 5, 2013
Creatine and guanidinoacetate reference values in a French populationMarie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|September 17, 2011
Motor and respiratory heterogeneity in Duchenne patients: implication for clinical trialsVéronique Humbertclaude, Dalil Hamroun, Kamel Bezzou, et al.
Journal of Medical Genetics|November 1, 2022
New insights into <i>CC2D2A</i>-related Joubert syndromeMadeleine Harion, Leila Qebibo, Audrey Riquet, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
Mosaic parental germline mutations causing recurrent forms of malformations of cortical developmentJulia Lauer Zillhardt, Karine Poirier, Loïc Broix, et al.
Pageof 135