Search research articles
Contact Us
Filters
Showing results (31-40 of 41) with videos related to
Page
of 5
Sort By:
Parkinsonism & Related Disorders
|
July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology
Giacomo 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 strategies
Jana 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 departments
Umberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Movement Disorders Clinical Practice
|
June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be Missed
Alice Innocenti, Emmanuel Roze, Florence Riant, et al.
Pediatrics
|
August 1, 2020
Characteristics of Acute Nystagmus in the Pediatric Emergency Department
Giacomo Garone, Agnese Suppiej, Nicola Vanacore, et al.
Clinical Genetics
|
July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness
Lorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Archives of Disease in Childhood
|
April 6, 2019
Acute ataxia in paediatric emergency departments: a multicentre Italian study
Giacomo 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 Dysfunction
Meredith 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 GNAO1
Thomas Wirth, Giacomo Garone, Manju A Kurian, et al.
JAMA Pediatrics
|
March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias
Mary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Parkinsonism & Related Disorders
|
July 27, 2024
Movement disorder phenotype in CTNNB1-syndrome: A complex but recognizable phenomenology
Giacomo 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 strategies
Jana 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 departments
Umberto Raucci, Pasquale Parisi, Nicola Vanacore, et al.
Movement Disorders Clinical Practice
|
June 12, 2025
ADCY5-Mosaic Variants: A Diagnosis Not to Be Missed
Alice Innocenti, Emmanuel Roze, Florence Riant, et al.
Pediatrics
|
August 1, 2020
Characteristics of Acute Nystagmus in the Pediatric Emergency Department
Giacomo Garone, Agnese Suppiej, Nicola Vanacore, et al.
Clinical Genetics
|
July 17, 2023
Congenital heart defects in CTNNB1 syndrome: Raising clinical awareness
Lorenzo Sinibaldi, Giacomo Garone, Alessandra Mandarino, et al.
Archives of Disease in Childhood
|
April 6, 2019
Acute ataxia in paediatric emergency departments: a multicentre Italian study
Giacomo 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 Dysfunction
Meredith 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 GNAO1
Thomas Wirth, Giacomo Garone, Manju A Kurian, et al.
JAMA Pediatrics
|
March 3, 2025
ATP1A3 Variants, Variably Penetrant Short QT Intervals, and Lethal Ventricular Arrhythmias
Mary E Moya-Mendez, Minu-Tshyeto Bidzimou, Padmapriya Muralidharan, et al.
Page
of 5