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Giacomo Garone

Showing results (31-40 of 41) with videos related to

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Parkinsonism & Related Disorders|July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenologyGiacomo Garone, Alice Innocenti, Melissa Grasso, et al.
Frontiers in Neurology|June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategiesJana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
Archives of Disease in Childhood|March 10, 2018
Acute hyperkinetic movement disorders in Italian paediatric emergency departmentsUmberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Movement Disorders Clinical Practice|June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be MissedAlice Innocenti, Emmanuel Roze, Florence Riant, et al.
Pediatrics|August 1, 2020
Characteristics of Acute Nystagmus in the Pediatric Emergency DepartmentGiacomo Garone, Agnese Suppiej, Nicola Vanacore, et al.
Clinical Genetics|July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awarenessLorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Archives of Disease in Childhood|April 6, 2019
Acute ataxia in paediatric emergency departments: a multicentre Italian studyGiacomo Garone, Antonino Reale, Nicola Vanacore, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
Children and Adolescent Patients with Variants in the <i>ATP1A3</i> -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node DysfunctionMeredith K Srour, Minu-Tshyeto K Bidzimou, Padmapriya Muralidharan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2022
Highlighting the Dystonic Phenotype Related to GNAO1Thomas Wirth, Giacomo Garone, Manju A Kurian, et al.
JAMA Pediatrics|March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular ArrhythmiasMary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Parkinsonism & Related Disorders|July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenologyGiacomo Garone, Alice Innocenti, Melissa Grasso, et al.
Frontiers in Neurology|June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategiesJana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
Archives of Disease in Childhood|March 10, 2018
Acute hyperkinetic movement disorders in Italian paediatric emergency departmentsUmberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Movement Disorders Clinical Practice|June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be MissedAlice Innocenti, Emmanuel Roze, Florence Riant, et al.
Pediatrics|August 1, 2020
Characteristics of Acute Nystagmus in the Pediatric Emergency DepartmentGiacomo Garone, Agnese Suppiej, Nicola Vanacore, et al.
Clinical Genetics|July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awarenessLorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Archives of Disease in Childhood|April 6, 2019
Acute ataxia in paediatric emergency departments: a multicentre Italian studyGiacomo Garone, Antonino Reale, Nicola Vanacore, et al.
Medrxiv : the Preprint Server for Health Sciences|September 10, 2024
Children and Adolescent Patients with Variants in the <i>ATP1A3</i> -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node DysfunctionMeredith K Srour, Minu-Tshyeto K Bidzimou, Padmapriya Muralidharan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 20, 2022
Highlighting the Dystonic Phenotype Related to GNAO1Thomas Wirth, Giacomo Garone, Manju A Kurian, et al.
JAMA Pediatrics|March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular ArrhythmiasMary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
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