Grzegorz Opala

Katowice, SL, Poland

Last Updated: 09/26/2026

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Found 33 publications

The history of Mayo Clinic Faculty Teaching Courses in Poland.

The history of Mayo Clinic Faculty Teaching Courses in Poland.

Journal: Neurologia i neurochirurgia polska

Published: December 21, 2025

Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis.

Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis.

Journal: International journal of molecular sciences

Published: April 23, 2022

Validation of the Polish version of the Unified Dyskinesia Rating Scale (UDysRS).

Validation of the Polish version of the Unified Dyskinesia Rating Scale (UDysRS).

Journal: Neurologia i neurochirurgia polska

Published: November 03, 2020

Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe.

Frequency of mutations in PRKN, PINK1, and DJ1 in Patients With Early-Onset Parkinson Disease from neighboring countries in Central Europe.

Journal: Parkinsonism & related disorders

Published: October 20, 2020

Validation of the Polish version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS).

Validation of the Polish version of the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS).

Journal: Neurologia i neurochirurgia polska

Published: April 15, 2020

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder.

Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder.

Journal: Brain : a journal of neurology

Published: April 06, 2017

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism.

Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism.

Journal: Brain : a journal of neurology

Published: March 09, 2016

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.

Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.

Journal: Neurology

Published: March 16, 2015

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies.

Journal: Neurology

Published: February 06, 2015

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.

Journal: European journal of neurology

Published: December 22, 2014

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease.

Journal: Neurology

Published: October 19, 2014

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease.

Large-scale assessment of polyglutamine repeat expansions in Parkinson disease.

Journal: Neurology

Published: October 08, 2014

Showing 1-12 of 33

Last Updated: 09/26/2026