Katarzyna Tońska

5PUBLICATIONS
10CO-AUTHORS
Optical technologyGenome structure and regulationOphthalmologyOptometryNeurology and neuromuscular diseases
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Publications (5)

|Jun 26, 2026
Analysis of genetic risk factors for Leber hereditary optic neuropathy in the Polish population.

|Aug 20, 2025
Ataxia and oculomotor apraxia caused by a large-scale deletion in the senataxin gene.

Joanna M Rusecka, Biruta Kierdaszuk, Iwona Stępniak

|Dec 23, 2023
<i>DNAJC30</i> Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients.

Anna Skorczyk-Werner, Katarzyna Tońska, Aleksandra Maciejczuk

|Aug 03, 2020
Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation.

Agnieszka Piotrowska-Nowak, Maciej R Krawczyński, Ewa Kosior-Jarecka

|Jan 19, 2018
Nuclear genes involved in mitochondrial diseases caused by instability of mitochondrial DNA.

Joanna Rusecka, Magdalena Kaliszewska, Ewa Bartnik

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Frequent Collaborators

3 joint publications

Maciej R Krawczyński

3 joint publications

Monika Ołdak

2 joint publications

Agnieszka Piotrowska-Nowak

2 joint publications

Magdalena Korwin