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Constantin Potagas

Showing results (71-80 of 78) with videos related to

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Brain : a Journal of Neurology|May 20, 2020
A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxiaMarianthi Breza, Thomas Bourinaris, Stephanie Efthymiou, et al.
Journal of the Neurological Sciences|October 17, 2022
Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek populationChrisoula Kartanou, Zoi Kontogeorgiou, Michail Rentzos, et al.
Neurology International|August 28, 2024
Precision Dopaminergic Treatment in a Cohort of Parkinson's Disease Patients Carrying Autosomal Recessive Gene Variants: Clinical Cohort Data and a Mini ReviewChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.
Journal of Neurology|August 9, 2023
Jumping to conclusions bias, psychosis and impulsivity in early stages of Parkinson's diseaseIoanna Pachi, Vassilis Papadopoulos, Lida Alkisti Xenaki, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Double Trouble: Association of Malignant Melanoma with Sporadic and Genetic Forms of Parkinson's Disease and Asymptomatic Carriers of Related Genes: A Brief ReportChristos Koros, Athina-Maria Simitsi, Anastasia Bougea, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 6, 2023
Impact of APOE Genotype on Cognition in Idiopathic and Genetic Forms of Parkinson's DiseaseChristos Koros, Kathrin Brockmann, Athina-Maria Simitsi, et al.
Parkinsonism & Related Disorders|May 6, 2025
Peripheral Immune pattern in a genetic cohort of p.A53T alpha-synuclein carriersChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2021
Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare DiseaseMarianthi Breza, Jennifer Hirst, Viorica Chelban, et al.
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Showing results (71-80 of 78) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 78 results.
Brain : a Journal of Neurology|May 20, 2020
A homozygous GDAP2 loss-of-function variant in a patient with adult-onset cerebellar ataxiaMarianthi Breza, Thomas Bourinaris, Stephanie Efthymiou, et al.
Journal of the Neurological Sciences|October 17, 2022
Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek populationChrisoula Kartanou, Zoi Kontogeorgiou, Michail Rentzos, et al.
Neurology International|August 28, 2024
Precision Dopaminergic Treatment in a Cohort of Parkinson's Disease Patients Carrying Autosomal Recessive Gene Variants: Clinical Cohort Data and a Mini ReviewChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.
Journal of Neurology|August 9, 2023
Jumping to conclusions bias, psychosis and impulsivity in early stages of Parkinson's diseaseIoanna Pachi, Vassilis Papadopoulos, Lida Alkisti Xenaki, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Double Trouble: Association of Malignant Melanoma with Sporadic and Genetic Forms of Parkinson's Disease and Asymptomatic Carriers of Related Genes: A Brief ReportChristos Koros, Athina-Maria Simitsi, Anastasia Bougea, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 6, 2023
Impact of APOE Genotype on Cognition in Idiopathic and Genetic Forms of Parkinson's DiseaseChristos Koros, Kathrin Brockmann, Athina-Maria Simitsi, et al.
Parkinsonism & Related Disorders|May 6, 2025
Peripheral Immune pattern in a genetic cohort of p.A53T alpha-synuclein carriersChristos Koros, Athina-Maria Simitsi, Nikolaos Papagiannakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2021
Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare DiseaseMarianthi Breza, Jennifer Hirst, Viorica Chelban, et al.
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