Association of ADORA1 rs2228079 and ADORA2A rs5751876 Polymorphisms with Gilles de la Tourette Syndrome in the Polish Population

Por Janik, Piotr, Berdyński, Mariusz, Safranow, Krzysztof, Żekanowski, Cezary
Publicado no PLoS One (2015)

A Novel MAPT Mutation, G55R, in a Frontotemporal Dementia Patient Leads to Altered Tau Function

Por Iyer, Abhinaya, LaPointe, Nichole E., Zielke, Krzysztof, Berdynski, Mariusz, Guzman, Elmer, Barczak, Anna, Chodakowska-Żebrowska, Małgorzata, Barcikowska, Maria, Feinstein, Stuart, Żekanowski, Cezary
Publicado em 2013

Two Desmin Gene Mutations Associated with Myofibrillar Myopathies in Polish Families

Por Fichna, Jakub Piotr, Karolczak, Justyna, Potulska-Chromik, Anna, Miszta, Przemyslaw, Berdynski, Mariusz, Sikorska, Agata, Filipek, Slawomir, Redowicz, Maria Jolanta, Kaminska, Anna, Zekanowski, Cezary
Publicado no PLoS One (2014)

PIN1 gene variants in Alzheimer's disease

Por Maruszak, Aleksandra, Safranow, Krzysztof, Gustaw, Katarzyna, Kijanowska-Haładyna, Beata, Jakubowska, Katarzyna, Olszewska, Maria, Styczyńska, Maria, Berdyński, Mariusz, Tysarowski, Andrzej, Chlubek, Dariusz, Siedlecki, Janusz, Barcikowska, Maria, Żekanowski, Cezary
Publicado em 2009

Intra-Familial Clinical Heterogeneity due to FTLD-U with TDP-43 Proteinopathy Caused by a Novel Deletion in Progranulin Gene (PGRN)

Por Gabryelewicz, Tomasz, Masellis, Mario, Berdynski, Mariusz, Bilbao, Juan M., Rogaeva, Ekaterina, St George-Hyslop, Peter, Barczak, Anna, Czyzewski, Krzysztof, Barcikowska, Maria, Wszolek, Zbigniew, Black, Sandra E., Zekanowski, Cezary
Publicado no J Alzheimers Dis (2010)

Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olf...

Por Markopoulou, Katerina, Chase, Bruce A., Robowski, Piotr, Strongosky, Audrey, Narożańska, Ewa, Sitek, Emilia J., Berdynski, Mariusz, Barcikowska, Maria, Baker, Matt C., Rademakers, Rosa, Sławek, Jarosław, Klein, Christine, Hückelheim, Katja, Kasten, Meike, Wszolek, Zbigniew K.
Publicado no PLoS One (2016)

Agraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?

Por Sitek, Emilia J., Narożańska, Ewa, Barczak, Anna, Jasińska-Myga, Barbara, Harciarek, Michał, Chodakowska-Żebrowska, Małgorzata, Kubiak, Małgorzata, Wieczorek, Dariusz, Konieczna, Seweryna, Rademakers, Rosa, Baker, Matt, Berdyński, Mariusz, Brockhuis, Bogna, Barcikowska, Maria, Żekanowski, Cezary, Heilman, Kenneth M., Wszołek, Zbigniew K., Sławek, Jarosław
Publicado em 2012