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M Repetto

Showing results (231-240 of 266) with videos related to

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Placenta|October 19, 2025
Chronic mild maternal stress modulates the immune response at the maternal-fetal interface and affects the growth and mortality of the offspringF L De la Cruz Borthiry, J S Beltrame, V A Cañumil, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
Nature Medicine|September 3, 2024
The WHO genomics program of work for equitable implementation of human genomics for global healthElena Ambrosino, Ahmad N Abou Tayoun, Marc Abramowicz, et al.
Human Molecular Genetics|April 27, 2024
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of functionMurat Alpaslan, Elodie Fastré, Sandrine Mestre, et al.
Movement Disorders Clinical Practice|February 7, 2025
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter StudyEmma N M M von Scheibler, Ann Swillen, Gabriela M Repetto, et al.
Therapeutic Advances in Endocrinology and Metabolism|June 2, 2018
Efficacy of gamification-based smartphone application for weight loss in overweight and obese adolescents: study protocol for a phase II randomized controlled trialPatrick Timpel, Fernando Henpin Yue Cesena, Christiane da Silva Costa, et al.
Frontiers in Pediatrics|December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous PopulationsCarla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2019
Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and BehaviorAvanti Gokhale, Cortnie Hartwig, Amanda A H Freeman, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|April 21, 2009
Development of a tandem-electrostatic-quadrupole accelerator facility for BNCTA J Kreiner, V Thatar Vento, P Levinas, et al.
European Journal of Human Genetics : EJHG|January 4, 2024
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in ChileM Cecilia Poli, Boris Rebolledo-Jaramillo, Catalina Lagos, et al.
Pageof 27

Showing results (231-240 of 266) with videos related to

Sort By:
Pageof 27
Placenta|October 19, 2025
Chronic mild maternal stress modulates the immune response at the maternal-fetal interface and affects the growth and mortality of the offspringF L De la Cruz Borthiry, J S Beltrame, V A Cañumil, et al.
Journal of Intellectual Disability Research : JIDR|February 22, 2022
The COVID-19 pandemic's impact on worry and medical disruptions reported by individuals with chromosome 22q11.2 copy number variants and their caregiversL K White, T B Crowley, B Finucane, et al.
Nature Medicine|September 3, 2024
The WHO genomics program of work for equitable implementation of human genomics for global healthElena Ambrosino, Ahmad N Abou Tayoun, Marc Abramowicz, et al.
Human Molecular Genetics|April 27, 2024
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of functionMurat Alpaslan, Elodie Fastré, Sandrine Mestre, et al.
Movement Disorders Clinical Practice|February 7, 2025
Prevalence of Parkinson's Disease in 22q11.2 Deletion Syndrome: A Multicenter StudyEmma N M M von Scheibler, Ann Swillen, Gabriela M Repetto, et al.
Therapeutic Advances in Endocrinology and Metabolism|June 2, 2018
Efficacy of gamification-based smartphone application for weight loss in overweight and obese adolescents: study protocol for a phase II randomized controlled trialPatrick Timpel, Fernando Henpin Yue Cesena, Christiane da Silva Costa, et al.
Frontiers in Pediatrics|December 31, 2020
Barriers and Considerations for Diagnosing Rare Diseases in Indigenous PopulationsCarla S D'Angelo, Azure Hermes, Christopher R McMaster, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 6, 2019
Systems Analysis of the 22q11.2 Microdeletion Syndrome Converges on a Mitochondrial Interactome Necessary for Synapse Function and BehaviorAvanti Gokhale, Cortnie Hartwig, Amanda A H Freeman, et al.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|April 21, 2009
Development of a tandem-electrostatic-quadrupole accelerator facility for BNCTA J Kreiner, V Thatar Vento, P Levinas, et al.
European Journal of Human Genetics : EJHG|January 4, 2024
Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in ChileM Cecilia Poli, Boris Rebolledo-Jaramillo, Catalina Lagos, et al.
Pageof 27