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Genetic evaluation of patients with Alström syndrome in the Polish population.
Zmyslowska A, Borowiec M, Antosik K, Ploski R, Ciechanowska M, Iwaniszewska B, Jakubiuk-Tomaszuk A, Janczyk W, Krawczynski M, Salmonowicz B, Stelmach M, Mlynarski W. Zmyslowska A, et al. Among authors: janczyk w. Clin Genet. 2016 Apr;89(4):448-453. doi: 10.1111/cge.12656. Epub 2015 Sep 24. Clin Genet. 2016. PMID: 26283575
Clinical presentations of Wilson disease among Polish children.
Naorniakowska M, Dądalski M, Kamińska D, Jańczyk W, Lebensztejn D, Fyderek K, Wysocki J, Socha P. Naorniakowska M, et al. Among authors: janczyk w. Dev Period Med. 2016;20(3):216-221. Dev Period Med. 2016. PMID: 27941192
Early Onset of Wilson Disease: Diagnostic Challenges.
Wiernicka A, Dądalski M, Jańczyk W, Kamińska D, Naorniakowska M, Hüsing-Kabar A, Schmidt H, Socha P. Wiernicka A, et al. Among authors: janczyk w. J Pediatr Gastroenterol Nutr. 2017 Nov;65(5):555-560. doi: 10.1097/MPG.0000000000001700. J Pediatr Gastroenterol Nutr. 2017. PMID: 28753182
A heterozygous mutation in GOT1 is associated with familial macro-aspartate aminotransferase.
Kulecka M, Wierzbicka A, Paziewska A, Mikula M, Habior A, Janczyk W, Dabrowska M, Karczmarski J, Lazniewski M, Ginalski K, Czlonkowska A, Socha P, Ostrowski J. Kulecka M, et al. Among authors: janczyk w. J Hepatol. 2017 Nov;67(5):1026-1030. doi: 10.1016/j.jhep.2017.07.003. Epub 2017 Jul 15. J Hepatol. 2017. PMID: 28716744 Free article.
29 results