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Medycyna Wieku Rozwojowego|October 18, 2011
[Transient bullous lesions - a case of de novo mutation in the COL7A1 gene in patient with Epidermolysis bullosa dystrophica]Agnieszka Sobczyńska-Tomaszewska, Katarzyna Wertheim-Tysarowska, Ewa Kosykowska, et al.Developmental Period Medicine|March 17, 2016
Genetic analysis in inherited metabolic disorders--from diagnosis to treatment. Own experience, current state of knowledge and perspectivesKatarzyna Wertheim-Tysarowska, Monika Gos, Jolanta Sykut-Cegielska, et al.Scientific Reports|April 24, 2025
Increased risk of anxiety and coping strategies in patients with selected genodermatoses with cornification disruptionMagdalena Fryze, Radoslaw Mlak, Aleksandra Kulbaka, et al.Experimental Dermatology|July 2, 2014
Novel KRT14 mutation causing epidermolysis bullosa simplex with variable phenotypeMarek Jankowski, Katarzyna Wertheim-Tysarowska, Rafal Jakubowski, et al.Journal of Clinical Medicine|July 15, 2026
Selected Vascular, Inflammatory, and Lipid Parameters in Patients with Selected Keratinization Disorders: Preliminary Data from a Retrospective Observational StudyAldona Pietrzak, Jakub Kęsik, Radosław Mlak, et al.Postepy Dermatologii I Alergologii|February 19, 2021
The analysis of echocardiographic results in patients suffering from epidermolysis bullosaKatarzyna Kurnicka, Katarzyna Osipowicz, Olga Dzikowska-Diduch, et al.The Journal of Pediatrics|June 14, 2011
Novel de novo large deletion in cystic fibrosis transmembrane conductance regulator gene results in a severe cystic fibrosis phenotypeAleksandra Norek, Marta Stremska, Agnieszka Sobczyńska-Tomaszewska, et al.Acta Dermatovenerologica Croatica : ADC|May 14, 2015
Hypercalciuria in a child with acral peeling skin syndrome: a case reportDaiva Gorczyca, Jolanta Węgłowska, Anna Prescha, et al.Postepy Dermatologii I Alergologii|February 7, 2022
Efficacy of gentamicin 0.3% solution of oral erosions healing in patients with severe generalized recessive dystrophic epidermolysis bullosa and its impact on the expression of type VII collagenKatarzyna Osipowicz, Piotr Wychowanski, Pawel Nieckula, et al.Orphanet Journal of Rare Diseases|May 25, 2021
The genetic basis of classical galactosaemia in Polish patientsAleksandra Jezela-Stanek, Anna Bauer, Katarzyna Wertheim-Tysarowska, et al.Pageof 5