Mateusz Biela
11PUBLICATIONS
31CO-AUTHORS
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Publications (11)
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|Dec 11, 2025
Neurodevelopmental Disorder with Psychomotor Delay, Hearing Loss, and Spasticity Caused by Compound Heterozygous SPATA5L1 Variants-Expanding Phenotype.Artur Polczyk, Ewelina Wolańska, Anna Zimny
|Oct 26, 2024
The Advancement of Appendicitis in Children in the Pre-Pandemic and the Pandemic Year.Marcin Jerzy Owczarzak, Mateusz Biela, Mateusz Paplicki
|Oct 18, 2024
Epigenomic and phenotypic characterization of DEGCAGS syndrome.Karim Karimi, Denisa Weis, Ingvild Aukrust
|Oct 11, 2023
A novel non-recurrent CNV deletion involving TBX4 and leaving TBX2 intact causes congenital alveolar dysplasia.Katarzyna Bzdęga, Mateusz Biela, Gail H Deutsch
|Jul 27, 2022
Prenatal Diagnosis of Jeune Syndrome Caused by Compound Heterozygous Variants in DYNC2H1 Gene-Case Report with Rapid WES Procedure and Differential Diagnosis of Lethal Skeletal Dysplasias.Agnieszka Stembalska, Małgorzata Rydzanicz, Magdalena Klaniewska
|May 28, 2022
Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene.Agnieszka Stembalska, Małgorzata Rydzanicz, Wojciech Walas
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Frequent Collaborators
7 joint publications
Rafal Ploski
5 joint publications
Malgorzata Rydzanicz
4 joint publications
Robert Smigiel
2 joint publications
Agnieszka Stembalska
2 joint publications
Magdalena Klaniewska
2 joint publications
Piotr Gasperowicz
1 joint publications
Lucie Dupuis
1 joint publications
Agnieszka Zubkiewicz-Kucharska
1 joint publications
Thomas Kitzler
1 joint publications
Neveen A Soliman
