Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Michele L. Rajput"'
Publikováno v:
Neurology
Objective:To identify the significance of baseline motor features to the lifelong prognostic motor subtypes in a Parkinson disease (PD) cohort.Methods:In a previous study of 166 PD cases, we observed different prognosis in tremor-dominant, akinetic-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8b14d6628c611eac188212f2f3da023
https://doi.org/10.1212/wnl.0000000000004078
https://doi.org/10.1212/wnl.0000000000004078
Publikováno v:
Parkinsonism & Related Disorders. 21:1232-1237
Background Definite diagnosis of idiopathic Parkinson's disease is based on histological findings of marked substantia nigra neuronal loss and Lewy body inclusions. Almost all cases with clinical diagnosis of idiopathic Parkinson's disease are treate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b95d31d8bdbc557d6c0f0f892c45de2
https://doi.org/10.1016/j.parkreldis.2015.08.029
https://doi.org/10.1016/j.parkreldis.2015.08.029
Autor:
Irene Meissner, James Torner, John Huston, Michele L. Rajput, David O. Wiebers, Lyell K. Jones, Robert D. Brown
Publikováno v:
Journal of Neurosurgery. 116:1238-1241
Object Investigators conducting the International Study of Unruptured Intracranial Aneurysms, sponsored by the National Institutes of Health, sought to evaluate predictors of future hemorrhage in patients who had unruptured mirror aneurysms. These pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d199a29b84f895d842aafe4f7db9519
https://doi.org/10.3171/2012.1.jns11779
https://doi.org/10.3171/2012.1.jns11779
Autor:
Alex Rajput, Ali H. Rajput, Matthew J. Farrer, Owen A. Ross, Sarah Lincoln, Carles Vilariño-Güell, Stephanie A. Cobb, Michael G. Heckman, Alexandra I. Soto-Ortolaza, Michele L. Rajput
Publikováno v:
Movement Disorders. 24:2411-2414
Alpha-synuclein gene (SNCA) mutations cause familial Parkinsonism but the role of SNCA variability in idiopathic Parkinson's disease (PD) remains incompletely defined. We report a study of SNCA genetic variation in 452 idiopathic PD cases and 245 con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16abf93ffb0d0fbcce1499bc0bc3faa1
https://doi.org/10.1002/mds.22795
https://doi.org/10.1002/mds.22795
Publikováno v:
Neurology. 73:206-212
Background: Individual variations in the course of Lewy body Parkinson disease (PD) are well known. Patients have been classified into different clinical subtypes to identify differences in the course among the subgroups. Several studies indicate tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::422eb4919c6828b5901f6d17bf876e29
https://doi.org/10.1212/wnl.0b013e3181ae7af1
https://doi.org/10.1212/wnl.0b013e3181ae7af1
Autor:
Jeremy T. Stone, Matthew J. Farrer, Sarah Lincoln, Christian Wider, Michele L. Rajput, Kristoffer Haugarvoll, Alex Rajput, J. Mark Gibson, Timothy Lynch, Owen A. Ross, Jan O. Aasly, Ryan J. Uitti, Zbigniew K. Wszolek, Michael G. Heckman, Nancy N. Diehl
Publikováno v:
Neuroscience Letters. 453:9-11
Attempts at replicating the first genome-wide association study (GWAS) in Parkinson's disease (PD) have not successfully identified genetic risk factors. The present study reevaluates data from the GWAS and focuses on the SNP (rs11155313, located in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45a5e19ab09225391d41f409b6b17ce9
https://doi.org/10.1016/j.neulet.2009.02.009
https://doi.org/10.1016/j.neulet.2009.02.009
Publikováno v:
Movement Disorders. 24:630-632
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09374cf6de7fcc1c92515567473c0063
https://doi.org/10.1002/mds.22064
https://doi.org/10.1002/mds.22064
Autor:
Sarah Lincoln, Matthew J. Farrer, Alex Rajput, Michele L. Rajput, Stephanie A. Cobb, Christopher A. Robinson, Dennis W. Dickson, Owen A. Ross, Justus C. Dachsel
Publikováno v:
Neurology. 67:1506-1508
Lrrk2 G2019S is predominantly associated with alpha-synuclein-immunopositive Lewy body pathology. We have identified Family SK where Lrrk2 G2019S segregates with slowly progressive parkinsonism and the affected proband has tau-immunopositive neurofib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1ad81b8a835d387db7aa904e8cee728
https://doi.org/10.1212/01.wnl.0000240220.33950.0c
https://doi.org/10.1212/01.wnl.0000240220.33950.0c
Autor:
Alex Rajput, Christopher A. Robinson, Carles Vilariño-Güell, Jan O. Aasly, Brinda Shah, Zbigniew K. Wszolek, Lucia Tapia, Wyeth W. Wasserman, A. Jon Stoessl, Silke Appel-Cresswell, Dennis W. Dickson, Mary Encarnacion, Austen J. Milnerwood, Mattia Volta, Chelsea Szu-Tu, Heather Han, Daniel M. Evans, Bruce L. Guenther, Irene Yu, Dayne Beccano-Kelly, Matthew J. Farrer, Colin J. D. Ross, Frederick T. Pishotta, Emil K. Gustavsson, Holly E. Sherman, Joanne Trinh, Virginie Bernard, Martine Girard, Lise N. Munsie, Rachel A. Gibson, Peter S. McPherson, Fayçal Hentati, Christina Thompson, Igor Tatarnikov, Owen A. Ross, Ali H. Rajput, Ruey-Meei Wu, Patrick Chou, Michelle K. Lin, Michele L. Rajput
A Saskatchewan multi-incident family was clinically characterized with Parkinson disease (PD) and Lewy body pathology. PD segregates as an autosomal-dominant trait, which could not be ascribed to any known mutation. DNA from three affected members wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::707adb32abe34682206e69f988c6cf09
https://europepmc.org/articles/PMC3999380/
https://europepmc.org/articles/PMC3999380/
Autor:
Michele L. Rajput
Publikováno v:
Canadian Journal of Cardiology. 32:1261.e7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e51c4074e86adc4c0e9162f8cb973fe
https://doi.org/10.1016/j.cjca.2015.12.016
https://doi.org/10.1016/j.cjca.2015.12.016