Magdalena Kaliszewska

Warsaw, MZ 02106, Poland

Last Updated: 09/26/2026

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Found 12 publications

Ataxia and oculomotor apraxia caused by a large-scale deletion in the senataxin gene.

Ataxia and oculomotor apraxia caused by a large-scale deletion in the senataxin gene.

Journal: Journal of applied genetics

Published: May 21, 2025

Comprehensive non-invasive assessment of electrocardiographic abnormalities and cardiac arrhythmias in patients with genetically confirmed mitochondrial diseases.

Comprehensive non-invasive assessment of electrocardiographic abnormalities and cardiac arrhythmias in patients with genetically confirmed mitochondrial diseases.

Journal: Journal of electrocardiology

Published: December 17, 2020

Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation.

Progressive External Ophthalmoplegia in Polish Patients-From Clinical Evaluation to Genetic Confirmation.

Journal: Genes

Published: December 11, 2020

Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".

Answer to Finsterer about "Multisystem presentation of a homozygous POLG2 variant".

Journal: European journal of medical genetics

Published: February 21, 2020

Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.

Whole exome sequencing identifies a homozygous POLG2 missense variant in an adult patient presenting with optic atrophy, movement disorders, premature ovarian failure and mitochondrial DNA depletion.

Journal: European journal of medical genetics

Published: April 04, 2019

The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort.

The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort.

Journal: Mitochondrion

Published: July 28, 2018

Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA.

Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA.

Journal: Journal of applied genetics

Published: December 07, 2017

Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts.

Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts.

Journal: Metabolic brain disease

Published: October 23, 2016

Identification of the first in Poland CACNA1A gene mutation in familial hemiplegic migraine. Case report.

Identification of the first in Poland CACNA1A gene mutation in familial hemiplegic migraine. Case report.

Journal: Neurologia i neurochirurgia polska

Published: August 08, 2016

Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease.

Yeast model analysis of novel polymerase gamma variants found in patients with autosomal recessive mitochondrial disease.

Journal: Human genetics

Published: April 01, 2015

Mitochondrial encephalomyopathy: towards diagnosis. A case report.

Mitochondrial encephalomyopathy: towards diagnosis. A case report.

Journal: Neurologia i neurochirurgia polska

Published: January 01, 2013

Molecular investigations of mitochondrial deletions: evaluating the usefulness of different genetic tests.

Molecular investigations of mitochondrial deletions: evaluating the usefulness of different genetic tests.

Journal: Gene

Published: April 19, 2012

Showing 1-12 of 12

Last Updated: 09/26/2026