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Journal of Clinical Medicine|September 27, 2025
Impact of <i>CARD14 rs34367357</i> Mutation, Nutrition Status, and Seasonality on the Response to Biologic Therapy in Psoriasis-A Retrospective Observational Single-Center StudyMichał Niedźwiedź, Agnieszka Czerwińska, Janusz Krzyścin, et al.Postepy Dermatologii I Alergologii|January 23, 2023
Gut microbiota in alopecia areataKarolina Brzychcy, Izabela Dróżdż, Sebastian Skoczylas, et al.Microorganisms|November 27, 2025
Evaluation of the Oral Microbiome in Patients with Alström and Bardet-Biedl Syndromes and Their Heterozygous Family MembersEwa Zmysłowska-Polakowska, Tomasz Płoszaj, Sebastian Skoczylas, et al.International Journal of Molecular Sciences|February 24, 2024
Screening for Rare Mitochondrial Genome Variants Reveals a Potentially Novel Association between <i>MT-CO1</i> and <i>MT-TL2</i> Genes and Diabetes PhenotypeTomasz Płoszaj, Sebastian Skoczylas, Karolina Gadzalska, et al.Current Oncology (Toronto, Ont.)|January 27, 2026
Germline <i>BRCA1/2</i> Variants in Polish Patients with Family History of Breast and Ovarian Cancer: Prevalence, CNV Detection, and Identification of a Novel Loss-of-Function MutationSebastian Skoczylas, Tomasz Płoszaj, Izabela Dróżdż, et al.Healthcare (Basel, Switzerland)|July 13, 2024
Transient Neonatal Diabetes Mellitus with an Unknown Cause in a 1-Month-Old Infant: A Case ReportMateusz Tarasiewicz, Anna Pietrzykowska, Julia Włodarczyk, et al.Neurogenetics|January 7, 2026
Neurological manifestations of Allgrove syndrome in patients carrying a potentially founder p.Ser263Pro variant in the AAAS geneEwa Juścińska, Karolina Gadzalska, Paulina Jakiel, et al.Biomedicines|October 29, 2025
The Clinical and Diagnostic Characterization of 6q24-Related Transient Neonatal Diabetes Mellitus: A Polish Pediatric Cohort StudyMichał Pietrusiński, Julia Grzybowska-Adamowicz, Tomasz Płoszaj, et al.Metabolites|April 27, 2026
Selected Brain Metabolites and Mitochondrial DNA Copy Number as Potential Markers of Ongoing Neurodegeneration in Patients with Wolfram SyndromeEwa Zmysłowska-Polakowska, Tomasz Płoszaj, Sebastian Skoczylas, et al.Neurogenetics|March 26, 2025
Mitochondrial DNA variants revealed by whole exome sequencing: from screening to diagnosis and follow-upSebastian Skoczylas, Tomasz Płoszaj, Karolina Gadzalska, et al.Pageof 2