Anna Sulek

11PUBLICATIONS
16CO-AUTHORS
Neurology and neuromuscular diseasesMajor global burdens of diseaseNeurogeneticsCancer diagnosisCondensed matter characterisation technique development
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Publications (11)

|May 26, 2025
Frequently observed polyneuropathy expands phenotypic spectrum of apparently pure autosomal dominant hereditary spastic paraplegias.

Iwona Stępniak, Maria Rakowicz, Wanda Lipczyńska-Łojkowska

|Apr 17, 2025
CANVAS as example of genetic and clinical complexity of RFC1-related disorders.

Filip Tomczuk, Anna Sulek, Piotr Janik

|Dec 16, 2024
Secretome - the role of extracellular vesicles in the pathogenesis and therapy of neurodegenerative diseases.

Anna Sulek

|Aug 10, 2024
The New Face of Dynamic Mutation-The CAA [CAG]n CAA CAG Motif as a Mutable Unit in the TBP Gene Causative for Spino-Cerebellar Ataxia Type 17.

Dorota Hoffman-Zacharska, Anna Sulek

|Aug 09, 2024
Co-occurrence of CAPN3 homozygous mutation and CCTG expansion in the CNBP gene in a patient with muscular dystrophy.

Wiktoria Radziwonik-Frączyk, Ewelina Elert-Dobkowska, Jolanta Kubalska

|May 11, 2024
SPAST Intragenic CNVs Lead to Hereditary Spastic Paraplegia via a Haploinsufficiency Mechanism.

Ewelina Elert-Dobkowska, Iwona Stepniak, Wiktoria Radziwonik-Fraczyk

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Frequent Collaborators

3 joint publications

Ewelina Elert-Dobkowska

2 joint publications

Iwona Stepniak

2 joint publications

Wiktoria Radziwonik-Frączyk

1 joint publications

Anna Sobanska