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Journal of Pediatric Gastroenterology and Nutrition|September 28, 2016
The Etiology and Clinical Course of Chronic Pancreatitis in Children With Early Onset of the DiseaseKarolina Wejnarska, Elwira Kolodziejczyk, Katarzyna Wertheim-Tysarowska, et al.Journal of Applied Genetics|November 20, 2017
Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single familyKatarzyna Niepokój, Agnieszka M Rygiel, Piotr Jurczak, et al.Experimental Dermatology|September 22, 2018
A novel de novo mutation p.Ala428Asp in KRT5 gene as a cause of localized epidermolysis bullosa simplexMarta Stawczyk-Macieja, Katarzyna Wertheim-Tysarowska, Rafał Jakubowski, et al.European Journal of Dermatology : EJD|January 24, 2012
Novel and recurrent COL7A1 mutation in a Polish populationKatarzyna Wertheim-Tysarowska, Agnieszka Sobczyńska-Tomaszewska, Cezary Kowalewski, et al.Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|May 1, 2019
The hybrid allele 1 of carboxyl-ester lipase (CEL-HYB1) in Polish pediatric patients with chronic pancreatitisGrzegorz Oracz, Aleksandra Anna Kujko, Karianne Fjeld, et al.American Journal of Medical Genetics. Part A|September 20, 2012
Disease-specific databases: why we need them and some recommendations from the Human Variome Project Meeting, May 28, 2011Heather J Howard, Arthur Beaudet, Vera Gil-da-Silva Lopes, et al.Journal of Pediatric Gastroenterology and Nutrition|October 3, 2017
Chymotrypsinogen C Genetic Variants, Including c.180TT, Are Strongly Associated With Chronic Pancreatitis in Pediatric PatientsAlicja Monika Grabarczyk, Grzegorz Oracz, Katarzyna Wertheim-Tysarowska, et al.Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|May 16, 2016
The clinical course of hereditary pancreatitis in children - A comprehensive analysis of 41 casesGrzegorz Oracz, Elwira Kolodziejczyk, Agnieszka Sobczynska-Tomaszewska, et al.Journal of Applied Genetics|January 14, 2025
Novel and recurrent genetic variants associated with male and female infertilityKatarzyna K Jankowska, Anna Kutkowska-Kazmierczak, Klaudia Ślusarczyk, et al.Przeglad Lekarski|May 14, 2011
[Analysis of causes and treatment of hearing loss in children from Department of Infant Diseases the Children's Memorial Health Institute, Warsaw]Bogumiła Milewska-Bobula, Bozena Lipka, Marzanna Radziszewska-Konopka, et al.Pageof 5