Associations of the eNOS G894T gene polymorphism with target organ damage in children with newly diagnosed primary hypertension

Bằng Śladowska-Kozłowska, Joanna, Litwin, Mieczysław, Niemirska, Anna, Wierzbicka, Aldona, Roszczynko, Marta, Szperl, Małgorzata
Xuất bản năm Pediatr Nephrol (2015)

Coexistence of Andersen–Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family

Bằng Jagodzińska, Michalina, Szperl, Małgorzata, Ponińska, Joanna, Kosiec, Agnieszka, Gajda, Robert, Kukla, Piotr, Biernacka, Elżbieta Katarzyna
Xuất bản năm Ann Noninvasive Electrocardiol (2015)

Evaluation of Head and Neck Paragangliomas by Computed Tomography in Patients with Pheochromocytoma-Paraganglioma Syndromes

Bằng Michałowska, Ilona, Lewczuk, Anna, Ćwikła, Jarosław, Prejbisz, Aleksander, Swoboda-Rydz, Urszula, Furmanek, Mariusz I., Szperl, Małgorzata, Januszewicz, Andrzej, Pęczkowska, Mariola
Xuất bản năm Pol J Radiol (2016)

MB-04 A NOVEL GERMLINE MUTATION IN ALK GENE (M1199L) IDENTYFIED IN THE WNT TYPE OF MEDULLOBLASTOMA

Bằng Trubicka, Joanna, Szperl, Malgorzata, Grajkowska, Wieslawa, Karkucinska-Wieckowska, Agnieszka, Tarasinska, Magdalena, Falana, Katarzyna, Perek-Polnik, Marta, Dembowska-Baginska, Bozenna, Lastowska, Maria
Xuất bản năm Neuro Oncol (2016)

Mediastinal paragangliomas related to SDHx gene mutations

Bằng Michałowska, Ilona, Ćwikła, Jarosław, Prejbisz, Aleksander, Kwiatek, Paweł, Szperl, Małgorzata, Michalski, Wojciech, Wyrwicz, Lucjan, Kuśmierczyk, Mariusz, Januszewicz, Andrzej, Maciejczyk, Anna, Roszczynko, Marta, Pęczkowska, Mariola
Xuất bản năm Kardiochir Torakochirurgia Pol (2016)

Andersen-Tawil Syndrome: Clinical presentation and predictors of symptomatic arrhythmias - possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene

Bằng Krych, Michalina, Biernacka, Elżbieta Katarzyna, Ponińska, Joanna, Kukla, Piotr, Filipecki, Artur, Gajda, Robert, Hasdemir, Can, Antzelevitch, Charles, Kosiec, Agnieszka, Szperl, Małgorzata, Płoski, Rafał, Trusz-Gluza, Maria, Mizia-Stec, Katarzyna, Hoffman, Piotr
Xuất bản năm J Cardiol (2017)

Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population

Bằng Paziewska, Agnieszka, Cukrowska, Bozena, Dabrowska, Michalina, Goryca, Krzysztof, Piatkowska, Magdalena, Kluska, Anna, Mikula, Michal, Karczmarski, Jakub, Oralewska, Beata, Rybak, Anna, Socha, Jerzy, Balabas, Aneta, Zeber-Lubecka, Natalia, Ambrozkiewicz, Filip, Konopka, Ewa, Trojanowska, Ilona, Zagroba, Malgorzata, Szperl, Malgorzata, Ostrowski, Jerzy
Xuất bản năm PLoS One (2015)

Titin Truncating Variants in Dilated Cardiomyopathy – Prevalence and Genotype-Phenotype Correlations

Bằng Franaszczyk, Maria, Chmielewski, Przemyslaw, Truszkowska, Grazyna, Stawinski, Piotr, Michalak, Ewa, Rydzanicz, Malgorzata, Sobieszczanska-Malek, Malgorzata, Pollak, Agnieszka, Szczygieł, Justyna, Kosinska, Joanna, Parulski, Adam, Stoklosa, Tomasz, Tarnowska, Agnieszka, Machnicki, Marcin M., Foss-Nieradko, Bogna, Szperl, Malgorzata, Sioma, Agnieszka, Kusmierczyk, Mariusz, Grzybowski, Jacek, Zielinski, Tomasz, Ploski, Rafal, Bilinska, Zofia T.
Xuất bản năm PLoS One (2017)