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Darryl C De Vivo

Showing results (1-10 of 192) with videos related to

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Journal of Child Neurology|February 25, 2003
Inherited metabolic disorders and seizures in infancyDarryl C De Vivo
Current Treatment Options in Neurology|April 3, 2001
Mitochondrial DiseaseRoser Pons, Darryl C. De Vivo
Clinical Obstetrics and Gynecology|September 24, 2021
Spinal Muscular Atrophy: A Potential Target for In Utero TherapyCaitlin Baptiste, Darryl C De Vivo
Annals of Neurology|March 13, 2010
Childhood absence epilepsy as a manifestation of GLUT1 deficiencyMichael Rotstein, Darryl C De Vivo
Future Neurology|March 21, 2014
Neurodegeneration in spinal muscular atrophy: from disease phenotype and animal models to therapeutic strategies and beyondUmrao R Monani, Darryl C De Vivo
Annals of Neurology|August 2, 2003
ForewordDarryl C De Vivo, Michael V Johnston
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2024
Reply to: Comment on De Giorgis et al. "Randomized Phase 3 Study of Triheptanoin for Glut1 Deficiency Syndrome-Associated Paroxysmal Movement Disorders"Valentina De Giorgis, Darryl C De Vivo
Journal of Child Neurology|February 25, 2003
Classification of infantile seizures: implications for identification and treatment of inborn errors of metabolismDouglas R Nordli, Darryl C De Vivo
Neurology|July 27, 2018
Precious SMA natural history data: A benchmark to measure future treatment successesBasil T Darras, Darryl C De Vivo
Journal of Child Neurology|February 25, 2003
Glucose transporter 1 deficiency syndrome and other glycolytic defectsDarryl C De Vivo, Linda Leary, Dong Wang
Pageof 20

Showing results (1-10 of 192) with videos related to

Sort By:
Pageof 20
Journal of Child Neurology|February 25, 2003
Inherited metabolic disorders and seizures in infancyDarryl C De Vivo
Current Treatment Options in Neurology|April 3, 2001
Mitochondrial DiseaseRoser Pons, Darryl C. De Vivo
Clinical Obstetrics and Gynecology|September 24, 2021
Spinal Muscular Atrophy: A Potential Target for In Utero TherapyCaitlin Baptiste, Darryl C De Vivo
Annals of Neurology|March 13, 2010
Childhood absence epilepsy as a manifestation of GLUT1 deficiencyMichael Rotstein, Darryl C De Vivo
Future Neurology|March 21, 2014
Neurodegeneration in spinal muscular atrophy: from disease phenotype and animal models to therapeutic strategies and beyondUmrao R Monani, Darryl C De Vivo
Annals of Neurology|August 2, 2003
ForewordDarryl C De Vivo, Michael V Johnston
Movement Disorders : Official Journal of the Movement Disorder Society|October 19, 2024
Reply to: Comment on De Giorgis et al. "Randomized Phase 3 Study of Triheptanoin for Glut1 Deficiency Syndrome-Associated Paroxysmal Movement Disorders"Valentina De Giorgis, Darryl C De Vivo
Journal of Child Neurology|February 25, 2003
Classification of infantile seizures: implications for identification and treatment of inborn errors of metabolismDouglas R Nordli, Darryl C De Vivo
Neurology|July 27, 2018
Precious SMA natural history data: A benchmark to measure future treatment successesBasil T Darras, Darryl C De Vivo
Journal of Child Neurology|February 25, 2003
Glucose transporter 1 deficiency syndrome and other glycolytic defectsDarryl C De Vivo, Linda Leary, Dong Wang
Pageof 20