Bibliografia UJ CM

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Kotaro Ogaki, Shunsuke Koga, Michael G. Heckman, Fabienne C. Fiesel, Maya Ando, Catherine Labbe, Oswaldo Lorenzo- Betancor,, Elisabeth L. Moussaud- Lamodiere, Alexandra I. Soto- Ortolaza, Ronald L. Walton, Audrey J. Strongosky, Ryan J. Uitti, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzinska, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Andreas Puschmann, Kenya Nishioka, Manabu Funayama, Nobutaka Hattori, Joseph E. Parisi, Ronald C. Petersen, Neill R. Graff-Radford, Bradley F. Boeve, Wolfdieter Springer, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross.
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
Neurology
2015 : Vol. 85, nr 23, s. 2016-2025, il., bibliogr., abstr.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
2/7
Catherine Labbe, Kotaro Ogaki, Lorenzo Lorenzo-Betancor,, Alexandra Soto-Ortolaza, Antony S. Walton, Sruti Rayaprolu, Shinsuke Fujioka, Melissa E. Murray, Michael G. Heckman, Andreas Puschmann, Allan McCarthy, Timothy Lynch, Joanna Siuda, Grzegorz Opala, Monika Rudzinska, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Yanosh Sanotsky, Irena Rektorova, Pamela J. McLean, Rosa Rademakers, Nilufer Ertekin-Taner, Anhar Hassan, J.Eric Ahlskog, Bradley F. Boeve, Ronald C. Petersen, Demetrius M. Maraganore, Charles H. Adler, Tanis J. Ferman, Joseph E. Parisi, Neill R. Graff-Radford, Ryan J. Uitti, Zbigniew K. Wszolek, Dennis W. Dickson, Owen A. Ross.
Role for the microtubule-associated protein tau variant p.A152T in risk of Α-synucleinopathies.
Neurology
2015 : Vol. 85, nr 19, s. 1680-1686
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.166
Adres url:
Streszczenie w PubMed:
3/7
Jessie Theuns, Aline Verstraeten, Kristel Sleegers, Eline Wauters, Ilse Gijselinck, Stefanie Smolders, David Crosiers, Ellen Corsmit, Ellen Elinck, Manu Sharma, Rejko Kruger, Suzanne Lesage, Alexis Brice, Sun Ju Chung, Mi-Jung Kim, Young Jin Kim, Owen A. Ross, Zbigniew K. Wszolek, Ekaterina Rogaeva, Zhengrui Xi, Anthony E. Lang, Christine Klein, Anne Weissbach, George D. Mellick, Peter A. Silburn, Georgios M. Hadjigeorgiou, Efthimios Dardiotis, Nobutaka Hattori, Ogaki Kotaro, Eng-King Tan, Yi Zhao, Jan Aasly, Enza Maria Valente, Simona Petrucci, Grazia Annesi, Aldo Quattrone, Carlo Ferrarese, Laura Brighina, Angela Deutschlnder, Andreas Puschmann, Christer Nilsson, Gaetan Garraux, Mark S. LeDoux, Ronald F. Pfeiffer, Magdalena Boczarska-Jedynak, Grzegorz Opala, Demetrius M. Maraganore, Sebastiaan Engelborghs, Peter Paul De Deyn, Patrick Cras, Marc Cruts, Christine Van Broeckhoven, GEO-PD Consortium.
Global investigation and meta-analysis of the C9orf72 (G₄C₂)n repeat in Parkinson disease.
Neurology
2014 : Vol. 83, nr 21, s. 1906-1913, il., bibliogr. 30 poz., abstr.
p-ISSN: 0028-3878
AZ
ORG
AIF
IF: 8.286
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Alexandra I. Soto-Ortolaza, Michael G. Heckman, Catherine Labbe, Daniel J. Serie, Andreas Puschmann, Sruti Rayaprolu, Audrey Strongosky, Magdalena Boczarska-Jedynak, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Krzysztof Czyzewski, Timothy Lynch, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
GWAS risk factors in Parkinson's disease: LRRK2 coding variation and genetic interaction with PARK16.
American Journal of Neurodegenerative Disease
2013 : Vol. 2, nr 4, s. 287-299, bibliogr. 23 poz., abstr.
p-ISSN: 2165-591X
AZ
ORG
APZ
Adres url:
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Mark S. LeDoux, Jianfeng Xiao, Monika Rudzińska, W. Bastian, Zbigniew K. Wszolek, Jay A. Van Gerpen, Andreas Puschmann, Dragana Momcilovic, Satya R. Vemula, Yu Zhao.
Genotype-phenotype correlations in THAP1 dystonia : Molecular foundations and description of new cases.
Parkinsonism & Related Disorders
2012 : Vol. 18, nr 5, s. 414-425, il., bibliogr. 52 poz., abstr.
p-ISSN: 1353-8020
AZ
POG
AIF
IF: 3.274
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Andreas Puschmann, Christophe Verbeeck, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Timothy Lynch, Barbara Jasinska-Myga, Grzegorz Opala, Anna Krygowska-Wajs, Maria Barcikowska, Ryan J. Uitti, Zbigniew K. Wszolek, Owen A. Ross.
Human leukocyte antigen variation and Parkinson's disease.
Parkinsonism & Related Disorders
2011 : Vol. 17, nr 5, s. 376-378, bibliogr. 12 poz., abstr.
p-ISSN: 1353-8020
AZ
ORG
AIF
IF: 3.795
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Carles Vilarino-Guell, C. Wider, Owen A. Ross, Justus C. Dachsel, Jennifer M. Kachergus, Sarah J. Lincoln, Alexandra I. Soto-Ortolaza, Stephanie A. Cobb, Greggory J. Wilhoite, Justin A. Bacon, Bahareh Behrouz, Heather A. Melrose, Emna Hentati, Andreas Puschmann, Daniel M. Evans, Elizabeth Conibear, Wyeth W. Wasserman, Jan O. Aasly, Pierre R. Burkhard, Ruth Djaldetti, Joseph Ghika, Faycal Hentati, Anna Krygowska-Wajs, Tim Lynch, Eldad Melamed, Alex Rajput, Ali H. Rajput, Alessandra Solida, Ruey-Meei Wu, Ryan J. Uitti, Zbigniew K. Wszolek, Francois Vingerhoets, Matthew J. Farrer.
VPS35 mutations in Parkinson disease.
American Journal of Human Genetics
2011 : Vol. 89, nr 1, s. 162-167, bibliogr. 24 poz.
p-ISSN: 0002-9297
AZ
ORG
AIF
IF: 10.603
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