CFTR mutations spectrum and the efficiency of molecular diagnostics in Polish cystic fibrosis patients.

by Ewa Ziętkiewicz, Ewa Rutkiewicz, Andrzej Pogorzelski, Barbara Klimek, Katarzyna Voelkel, Michał Witt
Published 2014-01-01

Ciliary genes are down-regulated in bronchial tissue of primary ciliary dyskinesia patients.

by Maciej Geremek, Ewa Ziętkiewicz, Marcel Bruinenberg, Lude Franke, Andrzej Pogorzelski, Cisca Wijmenga, Michał Witt
Published 2014-01-01

Assessment of Selected Parameters of Liver Fibrosis and Inflammation in Patients with Diagnosed Cystic Fibrosis

by Sabina Więcek, Halina Woś, Andrzej Pogorzelski, Bożena Kordys-Darmolinska, Henryk Mazurek, Urszula Grzybowska-Chlebowczyk
Published 2020-01-01

ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia.

by Małgorzata Kurkowiak, Ewa Ziętkiewicz, Agnieszka Greber, Katarzyna Voelkel, Alina Wojda, Andrzej Pogorzelski, Michał Witt
Published 2016-01-01

Mutations in radial spoke head genes and ultrastructural cilia defects in East-European cohort of primary ciliary dyskinesia patients.

by Ewa Ziętkiewicz, Zuzanna Bukowy-Bieryłło, Katarzyna Voelkel, Barbara Klimek, Hanna Dmeńska, Andrzej Pogorzelski, Anna Sulikowska-Rowińska, Ewa Rutkiewicz, Michał Witt
Published 2012-01-01

Prevalence and course of disease after lung resection in primary ciliary dyskinesia: a cohort & nested case-control study

by Panayiotis Kouis, Myrofora Goutaki, Florian S. Halbeisen, Ifigeneia Gioti, Nicos Middleton, Israel Amirav, on behalf of the Israeli PCD Consortium, Angelo Barbato, on behalf of the Italian PCD Consortium, Laura Behan, Mieke Boon, Nagehan Emiralioglu, Eric G. Haarman, Bulent Karadag, Cordula Koerner-Rettberg, Romain Lazor, on behalf of the Swiss PCD Group, Michael R. Loebinger, Bernard Maitre, on behalf of the French Reference Centre for Rare Lung Diseases, Henryk Mazurek, Lucy Morgan, Kim Gjerum Nielsen, Heymut Omran, Ugur Özçelik, Mareike Price, Andrzej Pogorzelski, Deborah Snijders, on behalf of the PCD Italian Consortium, Guillaume Thouvenin, on behalf of the French Reference Centre for Rare Lung Diseases, Claudius Werner, Zorica Zivkovic, Claudia E. Kuehni, Panayiotis K. Yiallouros
Published 2019-09-01