Zobrazeno 1 - 10
of 134
pro vyhledávání: '"Ali H, Rajput"'
Autor:
Eric Béliveau, Cyntia Tremblay, Émilie Aubry-Lafontaine, Sarah Paris-Robidas, Charlotte Delay, Chris Robinson, Les Ferguson, Ali H. Rajput, Alex Rajput, Frédéric Calon
Publikováno v:
Neurobiology of Disease, Vol 82, Iss , Pp 397-408 (2015)
The accumulation of insoluble amyloid-beta (Aβ) peptides is associated with neurodegenerative disorders, such as Alzheimer's disease (AD). As essential tremor (ET) could involve neurodegenerative processes in the cerebellum, we quantified soluble an
Externí odkaz:
https://doaj.org/article/779a09e5faa94a67994f52f072071c39
Autor:
Ali H. Rajput, Alex Rajput
Publikováno v:
Journal of Central Nervous System Disease, Vol 2014, Iss 6, Pp 29-39 (2014)
Externí odkaz:
https://doaj.org/article/55fe622e719f4c2ab9bc1787315fd0b8
Autor:
Stephen J. Kish, Ali H. Rajput
Publikováno v:
Movement Disorders
Autor:
Manuela Pendziwiat, Margaret E. Flanagan, Marla Gearing, Catriona McLean, Regina Reimann, Günter U. Höglinger, Günther Deuschl, Alan J. Thomas, David Ellinghaus, María José Martí, Allison Beller, Johannes Levin, Ian R. A. Mackenzie, Viktoria Ruf, John Q. Trojanowski, Jonathan D. Glass, Brit Mollenhauer, Franziska Hopfner, Justo Yebenes, Adriano Aguzzi, Lea T. Grinberg, Claire Troakes, Glenda M. Halliday, William K. Scott, Johannes Attems, Charles L. White, Ali H. Rajput, Kathy L. Newell, Owen A. Ross, Ulrich Müller, Charles Duyckaerts, Paula Desplats, Tao Xie, David J. Irwin, Inge Huitinga, Gerard D. Schellenberg, Valentin Evsyukov, Sashika Selvackadunco, Bernardino Ghetti, Per Svenningsson, Ian G. McKeith, Alex Rajput, Manuela Neumann, Ingo Helbig, Edward B. Lee, Ellen Gelpi, Jochen Herms, Tanya Simuni, Matthias Höllerhage, Matthew P. Frosch, Gregor Kuhlenbäumer, Andre Franke, Thomas G. Beach, Annette Peters, Dennis W. Dickson, Shunsuke Koga, Laura Molina Porcel, Vivianna M. Van Deerlin, Dirk C. Keene, Anja K. Tietz, Christine Stadelmann, Claudia Trenkwalder, Teresa Ximelis, William W. Seeley, Radoslav Matěj, Alexander Pantelyat, Alberto Rabano, Gabor G. Kovacs
Multiple System Atrophy is a rare neurodegenerative disease with alpha-synuclein aggregation in glial cytoplasmic inclusions and either predominant olivopontocerebellar atrophy or striatonigral degeneration, leading to dysautonomia, parkinsonism, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d159e4e330fd628ef6ab46fa3f884281
https://doi.org/10.1101/2021.11.11.21265915
https://doi.org/10.1101/2021.11.11.21265915
Autor:
Ali H. Rajput
Publikováno v:
Parkinsonism & Related Disorders. 78:195-197
Publikováno v:
Neurobiology of Disease, Vol 14, Iss 3, Pp 404-416 (2003)
Glutamate receptors were studied in the brains of controls and Parkinson's disease (PD) patients, of which 10 of 14 developed motor complications (dyskinesias and/or wearing-off) following levodopa therapy. 125I-RTI binding to the dopamine transporte
Externí odkaz:
https://doaj.org/article/bceb66a6745e4caeb197056dfa4767a1
Analysis of nuclear export sequence regions of FUS-Related RNA-binding proteins in essential tremor.
Autor:
Oswaldo Lorenzo-Betancor, Kotaro Ogaki, Alexandra Soto-Ortolaza, Catherine Labbé, Carles Vilariño-Güell, Alex Rajput, Ali H Rajput, Pau Pastor, Sara Ortega, Elena Lorenzo, Audrey J Strongosky, Jay A van Gerpen, Ryan J Uitti, Zbigniew K Wszolek, Owen A Ross
Publikováno v:
PLoS ONE, Vol 9, Iss 11, p e111989 (2014)
Genes encoding RNA-binding proteins, including FUS and TDP43, play a central role in different neurodegenerative diseases such as amyotrophic lateral sclerosis and frontotemporal lobar degeneration. Recently, a mutation located in the nuclear export
Externí odkaz:
https://doaj.org/article/f0fbe2e0f5234d98a8923bff591b4100
Publikováno v:
Parkinsonismrelated disorders. 86
Introduction Resting limb tremor (RLT) is a well known feature in parkinsonism. There is very little information on resting head tremor (RHT) in parkinsonism, and none in pathologically confirmed cases. The association between RLT and RHT remains unc
Autor:
Giulia Soldà, Roberto Cilia, Stefano Goldwurm, Alex Rajput, Kenya Nishioka, Nenad Blau, Alexander Young, Gianni Pezzoli, A. Jon Stoessl, Ilaria Guella, Vesna Sossi, Jordan Follett, Valeria Rimoldi, Nobutaka Hattori, Rosanna Asselta, Letizia Straniero, Ali H. Rajput, Stefano Duga, Laura Parkkinen, Matthew J. Farrer, Alberto Priori
Publikováno v:
Annals of Neurology. 82:640-646
Biallelic DNAJC12 mutations were described in children with hyperphenylalaninemia, neurodevelopmental delay, and dystonia. We identified DNAJC12 homozygous null variants (c.187A>T;p.K63* and c.79-2A>G;p.V27Wfs*14) in two kindreds with early-onset par
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