Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Y Sanotsky"'
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
Autor:
Ludmyla Fedoryshyn, Yuriy Matviyenko, Janice L. Holton, P V Kuzyk, Dorota Dziewulska, Y Sanotsky, Marianna Selikhova, Orest Semeryak, Andrew J. Lees
Publikováno v:
Movement disorders : official journal of the Movement Disorder SocietyReferences. 35(10)
Background A number of cases of severe parkinsonism-dystonia have been recognized and reported following the illicit use of ephedrone prepared from pseudoephedrine and potassium permanganate. The pathology associated with ephedrone neurotoxicity has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fb99c3f1352af8d89df2c53505ad799
https://pubmed.ncbi.nlm.nih.gov/32542919
https://pubmed.ncbi.nlm.nih.gov/32542919
Autor:
Y Sanotsky, Magdalena Boczarska-Jedynak, Ted M. Dawson, Matthew J. Farrer, Li Chen, Owen A. Ross, Fabienne C. Fiesel, Maya Ando, Thomas R. Caulfield, Roman Hudec, Monika Rudzińska-Bar, Joanna Siuda, Oskar Hansson, Kotaro Ogaki, Timothy Lynch, Grzegorz Opala, Andrzej Friedman, Peter A. Silburn, Valina L. Dawson, Dominika Truban, Elle D. James, Megha Mohan, Dariusz Koziorowski, Maria Swanberg, Michael G. Heckman, George D. Mellick, Itzia Jimenez-Ferrer, Carles Vilariño-Güell, Xu Hou, Wolfdieter Springer, Andreas Puschmann, Jan O. Aasly, Zbigniew K. Wszolek
Publikováno v:
Brain. 140:98-117
SEE GANDHI AND PLUN-FAVREAU DOI101093/AWW320 FOR A SCIENTIFIC COMMENTARY ON THIS ARTICLE: It has been postulated that heterozygous mutations in recessive Parkinson's genes may increase the risk of developing the disease. In particular, the PTEN-induc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6f3b7c1ce080a6f6bc91fa03ea30bc34
https://doi.org/10.1093/brain/aww261
https://doi.org/10.1093/brain/aww261
Autor:
Y Matvienko, L. Fedoryshyn, Marianna Selikhova, H Stanetska, Andrew J. Lees, M. Boychuk, I Komnatska, Y Sanotsky, Elina Tripoliti
Publikováno v:
Clinical Neurology and Neurosurgery. 147:71-77
Introduction In the last fifteen years a new cause of chronic manganese toxicity has been recognized. It follows recreational intravenous injections of Ephedrone, synthesized from a cold remedies contained pseudoephedrine. Potassium permanganate is u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39430edda45540e8bafee396a2577f8d
https://doi.org/10.1016/j.clineuro.2016.05.027
https://doi.org/10.1016/j.clineuro.2016.05.027
Autor:
Joanna Siuda, Megha Mohan, Grzegorz Opala, Y Sanotsky, Timothy Lynch, Ted M. Dawson, Jan O. Aasly, Michael G. Heckman, Kotaro Ogaki, Andreas Puschmann, Fabienne C. Fiesel, Peter A. Silburn, Zbigniew K. Wszolek, Dariusz Koziorowski, Owen A. Ross, Andrzej Friedman, Roman Hudec, Maya Ando, Thomas R. Caulfield, Carles Vilariño-Güell, Wolfdieter Springer, George D. Mellick, Magdalena Boczarska-Jedynak, M. Farrer, Elle D. James
Publikováno v:
Movement Disorders. 31:S1-S697
Objective: To investigate the possible disease-association and pathogenic mechanisms of heterozygous PINK1 mutations from a genetic, functional, and structural perspective. Background: It has been postulated that heterozygous mutations in recessive P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c8f98b1d3ff74aeb1a9748608b54dd2
https://doi.org/10.1002/mds.26688
https://doi.org/10.1002/mds.26688
Autor:
Jan O. Aasly, Oskar Hansson, Kotaro Ogaki, Matthew J. Farrer, Zbigniew K. Wszolek, Fabienne C. Fiesel, Monika Rudzińska-Bar, Joanna Siuda, Maya Ando, Thomas R. Caulfield, Megha Mohan, Magdalena Boczarska-Jedynak, Elle D. James, Li Chen, Grzegorz Opala, Y Sanotsky, Ted M. Dawson, Timothy Lynch, Andrzej Friedman, Peter A. Silburn, Owen A. Ross, Dominika Truban, Roman Hudec, Valina L. Dawson, Itzia Jimenez-Ferrer, Maria Swanberg, Andreas Puschmann, Michael G. Heckman, Dariusz Koziorowski, Wolfdieter Springer, George D. Mellick, Carles Vilariño-Güell, Xu Hou
Publikováno v:
Brain : a journal of neurology. 140(6)
We read with great interest that Gan-Or et al. (2017) have observed an association (albeit not reaching statistical significance) of the heterozygous PINK1 p.G411S mutation and rapid eye movement sleep behaviour disorder [RBD; effect size odds ratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c46bef43acc1de71ad2f207008e9bd0
https://pubmed.ncbi.nlm.nih.gov/28379291
https://pubmed.ncbi.nlm.nih.gov/28379291
Autor:
Stephen Sharman, Y Sanotsky, Atbin Djamshidian, Marianna Selikhova, Jenny Bearn, Ludmyla Fedoryshyn, Yuriy Matviyenko, Sean S. O'Sullivan, Bruno B. Averbeck, Andrew J. Lees, Yuriy Filts
Publikováno v:
Addiction. 108:771-779
Aims To examine a syndrome of chronic manganism that occurs in drug addicts in eastern Europe who use intravenous methcathinone (ephedrone) contaminated with potassium permanganate. In many cases the basal ganglia, especially the globus pallidus and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0f5b4e7bd2ebee9ee9c4fd042da8c56
https://doi.org/10.1111/add.12080
https://doi.org/10.1111/add.12080
Autor:
Yuriy Matviyenko, Y Sanotsky, Eileen M. Joyce, Atbin Djamshidian, Iciar Aviles-Olmos, Yuriy Filts, Stephen Sharman, Ludmyla Fedoryshyn, Rosanna Michalczuk, Karen M. Doherty, Thomas Foltynie, Marianna Selikhova, Bruno B. Averbeck, Henrietta Bowden-Jones, Andrew J. Lees, Sean S. O'Sullivan
Publikováno v:
Movement Disorders. 27:1137-1145
Links between impulsive-compulsive behaviors (ICBs) in treated Parkinson's disease (PD), behavioral addictions, and substance abuse have been postulated, but no direct comparisons have been carried out so far. We directly compared patients with PD wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9168c256d8bfc52a148b1c18bcccc30e
https://doi.org/10.1002/mds.25105
https://doi.org/10.1002/mds.25105
Autor:
Irena Rektorová, Ryan J. Uitti, Andreas Puschmann, Kotaro Ogaki, Oswaldo Lorenzo-Betancor, Maria Barcikowska, Neil Graff-Radford, Krzysztof Czyzewski, Carles Vilariño-Güell, Zbigniew K. Wszolek, Tanis J. Ferman, R. C. Petersen, Dennis W. Dickson, Wolfdieter Springer, B. F. Boeve, Anna Krygowska-Wajs, Grzegorz Opala, Audrey Strongosky, Catherine Labbé, Timothy Lynch, Owen A. Ross, Allan McCarthy, Pamela J. McLean, Y Sanotsky, Alexandra I. Soto-Ortolaza, Ronald L. Walton, Joseph E. Parisi, J.A. Van Gerpen, Matthew J. Farrer, Joanna Siuda
BackgroundRecently, a novel mutation in exon 24 of DNAJC13 gene (p.Asn855Ser, rs387907571) has been reported to cause autosomal dominant Parkinson's disease (PD) in a multi-incident Mennonite family. MethodsIn the present study the mutation containin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79a2ac76ad98b090a3a8fcb4f100051c
https://ruj.uj.edu.pl/xmlui/handle/item/95754
https://ruj.uj.edu.pl/xmlui/handle/item/95754
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