Andras Salamon

Szeged, CS, Hungary

Last Updated: 09/26/2026

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Found 30 publications

Case report: Adult presentation of glutaric aciduria type I.

Case report: Adult presentation of glutaric aciduria type I.

Journal: Ideggyogyaszati szemle

Published: August 05, 2026

Case report: VPS16 - a new cause of generalized dystonia

Case report: VPS16 - a new cause of generalized dystonia

Journal: Ideggyogyaszati szemle

Published: June 03, 2026

Clinical telemonitoring and telerehabilitation of cognition in rare neurological diseases: a scoping review.

Clinical telemonitoring and telerehabilitation of cognition in rare neurological diseases: a scoping review.

Journal: Journal of neurology

Published: April 14, 2026

Genetic epidemiology of C9orf72 repeat expansion associated amyotrophic lateral sclerosis in Hungary.

Genetic epidemiology of C9orf72 repeat expansion associated amyotrophic lateral sclerosis in Hungary.

Journal: Molecular medicine (Cambridge, Mass.)

Published: January 25, 2026

Expanding the Genetic and Phenotypic Spectrum of DYT-VPS16: The Importance of Splice-Site Variants.

Expanding the Genetic and Phenotypic Spectrum of DYT-VPS16: The Importance of Splice-Site Variants.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: July 30, 2025

Efficacy of Deep Brain Stimulation for the Treatment of Monogenic Dystonia Symptoms: A Systematic Review.

Efficacy of Deep Brain Stimulation for the Treatment of Monogenic Dystonia Symptoms: A Systematic Review.

Journal: European journal of neurology

Published: July 07, 2025

Device-Aided Treatment of Parkinsonism in Cerebrotendinous Xanthomatosis.

Device-Aided Treatment of Parkinsonism in Cerebrotendinous Xanthomatosis.

Journal: Movement disorders clinical practice

Published: December 17, 2024

The Application of Goal Attainment Scaling in Cervical Dystonia - An Exploratory Observational Pilot Study.

The Application of Goal Attainment Scaling in Cervical Dystonia - An Exploratory Observational Pilot Study.

Journal: Movement disorders clinical practice

Published: August 11, 2023

A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder.

A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder.

Journal: BMC pediatrics

Published: July 28, 2023

Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants.

Genetic Screening of a Hungarian Cohort with Focal Dystonia Identified Several Novel Putative Pathogenic Gene Variants.

Journal: International journal of molecular sciences

Published: June 01, 2023

Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin.

Clinical features of cervical dystonia patients classified by the COL-CAP concept and treated with ultrasound-guided botulinum neurotoxin.

Journal: Ideggyogyaszati szemle

Published: March 09, 2023

Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient.

Novel heterozygous STUB1 gene mutation causes SCA48 in a Hungarian patient.

Journal: Ideggyogyaszati szemle

Published: March 09, 2023

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Last Updated: 09/26/2026