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Roser Pons

Showing results (11-20 of 90) with videos related to

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Genes|July 29, 2023
A Case of Class I 17p13.3 Microduplication Syndrome with Unilateral Hearing LossSpiros Vittas, Maria Bisba, Georgia Christopoulou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2016
Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's diseaseRoser Pons, Kyriaki Kekou, Roubina Antonellou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2010
The spectrum of movement disorders in Glut-1 deficiencyRoser Pons, Abbie Collins, Michael Rotstein, et al.
Pediatric Blood & Cancer|March 31, 2021
Delayed-onset severe neurotoxicity related to blinatumomab in an adolescent patient with refractory acute lymphoblastic leukemiaMaria Filippidou, Georgia Avgerinou, Katerina Katsibardi, et al.
Seizure|May 23, 2018
Sleep architecture and epileptic characteristics of drug naïve patients in childhood absence epilepsy spectrum. A prospective studyArgirios Dinopoulos, Maria A Tsirouda, Anastasios Bonakis, et al.
Journal of Child Neurology|August 5, 2017
Upper Limb Function, Kinematic Analysis, and Dystonia Assessment in Children With Spastic Diplegic Cerebral Palsy and Periventricular LeukomalaciaRoser Pons, Athanasios Vanezis, Helen Skouteli, et al.
Movement Disorders Clinical Practice|July 1, 2025
Early Levodopa Therapy in Tyrosine Hydroxylase DeficiencyClaudio M de Gusmao, Roser Pons, Ganesh H Mochida, et al.
Journal of the Neurological Sciences|April 9, 2018
Intrafamilial variability in a polish family harbouring a frameshift THAP1 mutationMaria Stamelou, Simona Petrucci, Monia Ginevrino, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 4, 2011
Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European familiesRoser Pons, Ester Cuenca-León, Elena Miravet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2018
Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndromeAnna Papadopoulou, Argyrios Dinopoulos, George Koutsodontis, et al.
Pageof 9

Showing results (11-20 of 90) with videos related to

Sort By:
Pageof 9
Genes|July 29, 2023
A Case of Class I 17p13.3 Microduplication Syndrome with Unilateral Hearing LossSpiros Vittas, Maria Bisba, Georgia Christopoulou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2016
Analysis of a founder mutation in the TH gene in a cohort of greek patients with Parkinson's diseaseRoser Pons, Kyriaki Kekou, Roubina Antonellou, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 12, 2010
The spectrum of movement disorders in Glut-1 deficiencyRoser Pons, Abbie Collins, Michael Rotstein, et al.
Pediatric Blood & Cancer|March 31, 2021
Delayed-onset severe neurotoxicity related to blinatumomab in an adolescent patient with refractory acute lymphoblastic leukemiaMaria Filippidou, Georgia Avgerinou, Katerina Katsibardi, et al.
Seizure|May 23, 2018
Sleep architecture and epileptic characteristics of drug naïve patients in childhood absence epilepsy spectrum. A prospective studyArgirios Dinopoulos, Maria A Tsirouda, Anastasios Bonakis, et al.
Journal of Child Neurology|August 5, 2017
Upper Limb Function, Kinematic Analysis, and Dystonia Assessment in Children With Spastic Diplegic Cerebral Palsy and Periventricular LeukomalaciaRoser Pons, Athanasios Vanezis, Helen Skouteli, et al.
Movement Disorders Clinical Practice|July 1, 2025
Early Levodopa Therapy in Tyrosine Hydroxylase DeficiencyClaudio M de Gusmao, Roser Pons, Ganesh H Mochida, et al.
Journal of the Neurological Sciences|April 9, 2018
Intrafamilial variability in a polish family harbouring a frameshift THAP1 mutationMaria Stamelou, Simona Petrucci, Monia Ginevrino, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 4, 2011
Paroxysmal non-kinesigenic dyskinesia due to a PNKD recurrent mutation: report of two Southern European familiesRoser Pons, Ester Cuenca-León, Elena Miravet, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2018
Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndromeAnna Papadopoulou, Argyrios Dinopoulos, George Koutsodontis, et al.
Pageof 9