Peter Balicza

Tomo Street 25-29
Budapest, BU 1083, Hungary

Last Updated: 09/26/2026

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Found 29 publications

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 Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort.

Expanding the Phenotypic Spectrum of SPG7 Rare Damaging Variants: Insights From a Hungarian Cohort.

Journal: Clinical genetics

Published: October 24, 2024

Multilevel evidence of MECP2-associated mitochondrial dysfunction and its therapeutic implications.

Multilevel evidence of MECP2-associated mitochondrial dysfunction and its therapeutic implications.

Journal: Frontiers in psychiatry

Published: September 24, 2023

GBA-associated Parkinson's disease in Hungary: clinical features and genetic insights.

GBA-associated Parkinson's disease in Hungary: clinical features and genetic insights.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: July 23, 2023

MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.

MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans.

Journal: EMBO molecular medicine

Published: April 26, 2023

Genetic landscape of early-onset dementia in Hungary.

Genetic landscape of early-onset dementia in Hungary.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: January 30, 2022

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.

New Insights of Phospholipase A2 Associated Neurodegeneration Phenotype Based on the Long-Term Follow-Up of a Large Hungarian Family.

Journal: Frontiers in genetics

Published: November 13, 2020

Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene

Hereditary Parkinson’s disease as a new clinical manifestation of the damaged POLG gene

Journal: Orvosi hetilap

Published: May 05, 2020

Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability.

Novel dominant MPAN family with a complex genetic architecture as a basis for phenotypic variability.

Journal: Neurology. Genetics

Published: March 30, 2020

Wernicke-Korsakoff syndrome associated with mtDNA disease.

Wernicke-Korsakoff syndrome associated with mtDNA disease.

Journal: Therapeutic advances in neurological disorders

Published: February 01, 2020

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.

The Role of Genetic Testing in the Clinical Practice and Research of Early-Onset Parkinsonian Disorders in a Hungarian Cohort: Increasing Challenge in Genetic Counselling, Improving Chances in Stratification for Clinical Trials.

Journal: Frontiers in genetics

Published: April 30, 2019

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients.

Comprehensive Analysis of Rare Variants of 101 Autism-Linked Genes in a Hungarian Cohort of Autism Spectrum Disorder Patients.

Journal: Frontiers in genetics

Published: January 21, 2019

Showing 1-12 of 29

Last Updated: 09/26/2026