Zygmunt Jamrozik

Warsaw, MZ, Poland

Last Updated: 09/26/2026

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Found 19 publications

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

Clinical phenotype heterogeneity in a family with ε-sarcoglycan gene mutation.

Clinical phenotype heterogeneity in a family with ε-sarcoglycan gene mutation.

Journal: Neurologia i neurochirurgia polska

Published: July 19, 2019

Electrophysiological and clinical assessment of dysautonomia in multiple system atrophy (MSA) and progressive supranuclear palsy (PSP): a comparative study.

Electrophysiological and clinical assessment of dysautonomia in multiple system atrophy (MSA) and progressive supranuclear palsy (PSP): a comparative study.

Journal: Neurologia i neurochirurgia polska

Published: December 06, 2018

Serum amino acid profile in patients with Parkinson's disease.

Serum amino acid profile in patients with Parkinson's disease.

Journal: PloS one

Published: July 07, 2017

Diagnostic value of blink reflex in multisystem atrophy, progressive supranuclear palsy and Parkinson disease.

Diagnostic value of blink reflex in multisystem atrophy, progressive supranuclear palsy and Parkinson disease.

Journal: Neurologia i neurochirurgia polska

Published: March 15, 2016

Expression of RNAs Coding for Metal Transporters in Blood of Patients with Huntington's Disease.

Expression of RNAs Coding for Metal Transporters in Blood of Patients with Huntington's Disease.

Journal: Neurochemical research

Published: August 26, 2015

GSTP1 Polymorphisms and their Association with Glutathione Transferase and Peroxidase Activities in Patients with Motor Neuron Disease.

GSTP1 Polymorphisms and their Association with Glutathione Transferase and Peroxidase Activities in Patients with Motor Neuron Disease.

Journal: CNS & neurological disorders drug targets

Published: May 25, 2015

The role of neuroimaging in the diagnosis of the atypical parkinsonian syndromes in clinical practice.

The role of neuroimaging in the diagnosis of the atypical parkinsonian syndromes in clinical practice.

Journal: Neurologia i neurochirurgia polska

Published: April 14, 2015

A case report of amyotrophic lateral sclerosis in a patient with Klippel-Feil syndrome—a familial occurrence: a potential role of TGF-β signaling pathway.

A case report of amyotrophic lateral sclerosis in a patient with Klippel-Feil syndrome—a familial occurrence: a potential role of TGF-β signaling pathway.

Journal: Medicine

Published: January 31, 2015

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.

Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients.

Journal: Neurologia i neurochirurgia polska

Published: August 30, 2013

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.

Analysis of PITX3 gene in patients with multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration.

Journal: Annals of clinical and laboratory science

Published: May 23, 2013

Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.

Late onset GM2 gangliosidosis mimicking spinal muscular atrophy.

Journal: Gene

Published: April 18, 2013

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Last Updated: 09/26/2026