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Trends in Parasitology|February 4, 2012
Malaria's deadly secret: a skin stageD Lys Guilbride, Patrick D L Guilbride, Pawel Gawlinski
Cells|September 9, 2022
A Zebrafish/Drosophila Dual System Model for Investigating Human MicrocephalySlawomir Bartoszewski, Mateusz Dawidziuk, Natalia Kasica, et al.
International Journal of Molecular Sciences|January 21, 2022
De Novo ACTG1 Variant Expands the Phenotype and Genotype of Partial Deafness and Baraitser-Winter SyndromeMateusz Dawidziuk, Anna Kutkowska-Kazmierczak, Ewelina Bukowska-Olech, et al.
Journal of Applied Genetics|August 20, 2023
Congenital coenzyme Q5-linked pathology: causal genetic association, core phenotype, and molecular mechanismMateusz Dawidziuk, Aleksandra Podwysocka, Marta Jurek, et al.
Journal of Clinical Research in Pediatric Endocrinology|December 20, 2018
A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic PolyneuropathyJoanna Oswiecimska, Mateusz Dawidziuk, Tomasz Gambin, et al.
Pediatric Neurology|June 26, 2016
PEHO Syndrome May Represent Phenotypic Expansion at the Severe End of the Early-Onset EncephalopathiesPawel Gawlinski, Renata Posmyk, Tomasz Gambin, et al.
Nature Communications|January 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humansClaudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig, et al.
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