Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Katherine Karpinsky"'
Autor:
Lukasz M. Milanowski, Xu Hou, Jenny M. Bredenberg, Fabienne C. Fiesel, Liam T. Cocker, Alexandra I. Soto-Beasley, Ronald L. Walton, Audrey J. Strongosky, Ayman H. Faroqi, Maria Barcikowska, Magdalena Boczarska-Jedynak, Jaroslaw Dulski, Lyuda Fedoryshyn, Piotr Janik, Anna Potulska-Chromik, Katherine Karpinsky, Anna Krygowska-Wajs, Tim Lynch, Diana A. Olszewska, Grzegorz Opala, Aleksander Pulyk, Irena Rektorova, Yanosh Sanotsky, Joanna Siuda, Mariusz Widlak, Jaroslaw Slawek, Monika Rudzinska-Bar, Ryan Uitti, Monika Figura, Stanislaw Szlufik, Sylwia Rzonca-Niewczas, Elzbieta Podgorska, Pamela J. McLean, Dariusz Koziorowski, Owen A. Ross, Dorota Hoffman-Zacharska, Wolfdieter Springer, Zbigniew K. Wszolek
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 13; Pages: 7086
Parkinson’s disease (PD) is generally considered a sporadic disorder, but a strong genetic background is often found. The aim of this study was to identify the underlying genetic cause of PD in two affected siblings and to subsequently assess the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::226fa72689b0798b7cab5a43839b68ec
Autor:
Ronald L. Walton, Joanna Siuda, Zygmunt Jamrozik, Angela Deutschländer, Piotr Janik, Magdalena Boczarska-Jedynak, Maria Barcikowska, Katherine Karpinsky, Alexandra I. Soto-Beasley, Irena Rektorová, Lech Szczechowski, Andrzej Friedman, Dorota Hoffman-Zacharska, Barbara Jasinska-Myga, Dariusz Koziorowski, Jarosław Dulski, Jarosław Sławek, Jennifer A. Lindemann, Aleksander Pulyk, Katarzyna Śmiłowska, Lyuda Fedoryshyn, Zbigniew K. Wszolek, Owen A. Ross, Anna Potulska-Chromik, Gabriela Kłodowska, Grzegorz Opala, Monika Rudzińska-Bar, Y Sanotsky, Łukasz Milanowski, Anna Krygowska-Wajs
Publikováno v:
Parkinsonism Relat Disord
Introduction Approximately 10% of patients with Parkinson disease (PD) present with early-onset disease (EOPD), defined as diagnosis before 50 years of age. Genetic factors are known to contribute to EOPD, with most commonly observed mutations in PRK
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de6925eedb65d19a267889746da32b27
https://pubmed.ncbi.nlm.nih.gov/33845304
https://pubmed.ncbi.nlm.nih.gov/33845304