Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Katya, Kotschet"'
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 8, Iss , Pp 100179- (2023)
Objectives: The feasibility of measuring bradykinesia and chorea in Huntington's Disease using a wearable sensor system (Parkinson’s Kinetigraph: PKG) developed for measuring bradykinesia and dyskinesia in Parkinson’s Disease was assessed. Method
Externí odkaz:
https://doaj.org/article/2a713896b93b4b3487190b47655c2fcf
Publikováno v:
npj Parkinson's Disease, Vol 6, Iss 1, Pp 1-10 (2020)
NPJ Parkinson's Disease
NPJ Parkinson's Disease
Medical conditions with effective therapies are usually managed with objective measurement and therapeutic targets. Parkinson’s disease has effective therapies, but continuous objective measurement has only recently become available. This blinded,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::089c08046998259eab9ce138ec55901b
http://link.springer.com/article/10.1038/s41531-020-00136-9
http://link.springer.com/article/10.1038/s41531-020-00136-9
Autor:
Evelyn Berger-Sieczkowski, Gian Maria Asioli, Javier Villacieros-Álvarez, Katya Kotschet, Marcus Erdler, Joan Santamaria Cano, Carles Gaig, Teresa Montojo, Alejandro Herrero San Martin, Koldo Berganzo, Morten Blaabjerg, Günter U. Höglinger, Lydia Lopez Manzanares, Giuseppe Plazzi, Josep Dalmau, Thomas Seifert-Held, Maja Patalong-Ogiewa, Barbara Willekens, Federica Provini, Nicola Tambasco, Herburg Liendl, Yaroslau Compta, Jan Lewerenz, Ángela Milán-Tomás, Christian Geis, Alex Iranzo, Inmaculada Puertas, Caroline Giordana, Birgit Högl, Lidia Sabater, Antonio Martin-Bastida, Nora Möhn, Lucio Huebra, Sonia Quintas, Francesc Graus, Pasquale Nigro, Norbert Brüggemann, Markus Hutterer, Maarten J. Titulaer, Maria Elena Erro, Stefan Macher, Florian Schoeberl, N. Téllez, Mateus Mistieri Simabukuro, Franziska S. Thaler, Juan Carlos Garcia-Monco, Jesus Perez Perez, Romana Höftberger, Caspar B Seitz, Anna Heidbreder, Carlos Morata, Yvette S Crijnen, Chen Fei Ng, Tarsis Farias, María José Martí
Publikováno v:
Gaig, C, Compta, Y, Heidbreder, A, Marti, M J, Titulaer, M J, Crijnen, Y, Högl, B, Lewerenz, J, Erro, M E, Garcia-Monco, J C, Nigro, P, Tambasco, N, Patalong-Ogiewa, M, Erdler, M, Macher, S, Berger-Sieczkowski, E, Höftberger, R, Geis, C, Hutterer, M, Milán-Tomás, A, Martin-Bastida, A, Manzanares, L L, Quintas, S, Höglinger, G U, Möhn, N, Schoeberl, F, Thaler, F S, Asioli, G M, Provini, F, Plazzi, G, Berganzo, K, Blaabjerg, M, Brüggemann, N, Farias, T, Ng, C F, Giordana, C, Herrero-San Martín, A, Huebra, L, Kotschet, K, Liendl, H, Montojo, T, Morata, C, Perez, J P, Puertas, I, Seifert-Held, T, Seitz, C, Simabukuro, M M, Tellez, N, Villacieros-Álvarez, J, Willekens, B, Sabater, L, Iranzo, A, Cano, J S, Dalmau, J & Graus, F 2021, ' Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease ', Neurology, vol. 97, no. 14, pp. e1367-e1381 . https://doi.org/10.1212/WNL.0000000000012639
NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurology
NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Neurology
Background and ObjectivesAnti-IgLON5 disease is a recently described neurologic disease that shares features of autoimmunity and neurodegeneration. Abnormal movements appear to be frequent and important but have not been characterized and are underre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb9bfacd5b844fa5de099b0b5aa5518d
https://portal.findresearcher.sdu.dk/da/publications/bdf1ece5-6028-4911-a2d1-11bd881fcbd6
https://portal.findresearcher.sdu.dk/da/publications/bdf1ece5-6028-4911-a2d1-11bd881fcbd6
Autor:
Michael Hayes, Jason Gu, Neil Mahant, Karl Ng, Hugo Morales-Briceño, Kishore R. Kumar, G. M. Wali, Ryan L. Davis, Victor S.C. Fung, Zachary Walls, Michel Tchan, Chung Sen Phua, Sue Faye Siow, Sarah K. Kummerfeld, Florence C.F. Chang, Dominic B. Rowe, Stephen Tisch, André E. Minoche, P. Darveniza, Con Yiannikas, Velimir Gayevskiy, Ce Kang, Katya Kotschet, Stan Levy, Alex Drew, Carolyn M. Sue, Gautam Wali, Mark J. Cowley
Publikováno v:
Parkinsonism & Related Disorders. 69:111-118
Introduction Dystonia is a clinically and genetically heterogeneous disorder and a genetic cause is often difficult to elucidate. This is the first study to use whole genome sequencing (WGS) to investigate dystonia in a large sample of affected indiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a3ac0b1b6acd6b551a9df9081f69556
https://doi.org/10.1016/j.parkreldis.2019.11.004
https://doi.org/10.1016/j.parkreldis.2019.11.004
Autor:
Andrew H Evans, Jade Kettlewell, Sarah McGregor, Katya Kotschet, Robert I Griffiths, Malcolm Horne
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e89319 (2014)
OBJECTIVES: Parkinson's Disease patients wore a device on the wrist that gave reminders to take levodopa and also measured bradykinesia and dyskinesia. Consumption of medications was acknowledged by placing the thumb on the device. Some patients perf
Externí odkaz:
https://doaj.org/article/371242afe06c439687ea5df250cbb298
Autor:
Alberto Albanese, Janis M. Miyasaki, Ryuji Kaji, Connie Marras, Francisco Cardoso, Alberto J. Espay, Alexander Münchau, Emilia Gatto, Victor S.C. Fung, Gustavo Da Prat, Ludger Schöls, Joseph Jankovic, Andres de la Cerda, Marina A. J. Tijssen, Pedro J. Garcia-Ruiz, Hyder A. Jinnah, Kailash P. Bhatia, Maria Cruz Rodriguez Oroz, Pramod Kumar Pal, Oscar S. Gershanik, Mayela Rodríguez-Violante, Tom J. de Koning, Katya Kotschet, Francesca Morgante, Claudia Uribe Roca, Maria Stamelou
Publikováno v:
Movement Disorders. 33:21-35
There are many rare movement disorders, and new ones are described every year. Because they are not well recognized, they often go undiagnosed for long periods of time. However, early diagnosis is becoming increasingly important. Rapid advances in ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb8108c39679d8eca905e9dfd7cf0945
https://doi.org/10.1002/mds.27140
https://doi.org/10.1002/mds.27140
Autor:
Josep Dalmau, Caroline Giordana, Maria J. Martí, Lidia Sabater, Mateus Mistieri Simabukuro, Joan Santamaria, Luis Bataller, N. Téllez, Katya Kotschet, Norbert Brüggemann, Inmaculada Puertas, Jan Lewerenz, Klaus-Peter Wandinger, Carles Gaig, Birgit Högl, Teresa Montojo, Francesc Graus, Jesus Pérez-Pérez, Stefan Macher, Guadalupe Ercilla, A. Iranzo, Yarko Compta, Anna Heidbreder, Caspar Seitz
Publikováno v:
Neurology
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
NEUROLOGY
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Objective:To report the presentation, main syndromes, human leukocyte antigen (HLA) association, and immunoglobulin G (IgG) subclass in the anti-IgLON5 disease: a disorder with parasomnias, sleep apnea, and IgLON5 antibodies.Methods:This was a retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c738cf9cf779772e84e348b8cfe1653e
https://doi.org/10.1212/wnl.0000000000003887
https://doi.org/10.1212/wnl.0000000000003887
Autor:
Turner-Stokes, Lynne, Jacinto, Jorge, Fheodoroff, Klemens, Brashear, Allison, Maisonobe, Pascal, Lysandropoulos, Andreas, Ashford, Stephen on behalf of the Upper Limb International Spasticity-III (ULIS-III) study group( Australia: Ian Baguley, Arun, Aggarwal, John, Olver, John, Estell, Steven, Faux, Edwin, Luk, Katya, Kotschet, Andrew, Hughes, Austria and Germany: Bernhard Haslinger, Rachael Nunan., Petra, Baum, Cornelia, Mobius, Urban, Fietzek, Brazil: Tae Mo Chung, Chi Wang Ip., Régina Helena Chueire, France: Alexis Schnitzler, Carla Heloisa Cabral Moro., Claire, Delleci, Anne-Laure, Ferrapie, Marie-Eve, Isner-Horobeti, Italy: Michela Cosma, Dominic Perennou. Hong Kong: Ching Man Leung., Carlo, Caltagirone, Manuela, Diverio, Girlanda, Paolo, Giancarlo, Ianeri, Marzia, Millevolte, Mexico: Jorge Hernandez Franco, Franco Molteni., Juan Francisco Gomez Hernandez, Sandra Quinones Aguilar, Philippines: Raymond Rosales, Laura Patricia De La Lanza Andrade., Poland: Dariusz Koziorowski, Jeanne Flordelis., Anna, Potulska, Portugal: Eduarda Afonso, Monika Rudzinska., Russia: Svetlana Khatkova, Ana Rolo Duarte., Alexey, Korenko, Dina, Khasanova, Dmitry, Okhabov, Elena, Arefyeva, Denis, Karpov, Taiwan: Yi-Chung Lee, Andrey Korolev., USA: Jessica Tate, Sen-Wei Tsai., Davis, Thomas L., Cynthia, Marciniak, Atul, Patel. ).
Publikováno v:
Journal of Rehabilitation Medicine, Vol 53, Iss 2, p jrm00157 (2021)
Objective To assess the longitudinal effects of integrated spasticity management incorporating repeated cycles of botulinum toxin A type A (BoNT-A) over 2 years. Methods The Upper Limb International Spasticity study was a prospective, observational,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6aa80cd3e19e5c7df14ab7b1010a329a
https://doi.org/10.2340/16501977-2801
https://doi.org/10.2340/16501977-2801
Autor:
Katya Kotschet, Stuart Isaacson, Fatta B. Nahab, Diego Torres-Russotto, Peter Lynch, Rajesh Pahwa
Publikováno v:
Expert review of neurotherapeutics. 18(8)
Evaluation of people with Parkinson's disease (PD) is often complex due to heterogeneity of symptoms and disease course, including the variability of motor fluctuations and dyskinesia. Routine clinical evaluations may be incomplete, may not accuratel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::156b7917fbcd4571749780004aaeedeb
https://pubmed.ncbi.nlm.nih.gov/30032695
https://pubmed.ncbi.nlm.nih.gov/30032695
Autor:
Wenyi Wang, Carolyn M. Sue, Ella J Wilkins, Martin O'Hely, Justin P. Rubio, Terence P. Speed, Wah Chin Boon, Katya Kotschet, J. Stankovitch, Malcolm K. Horne, Tiffany F. Cowie, Rachel K. Burfoot
Publikováno v:
Parkinsonism & Related Disorders. 18:386-390
Parkinson's disease (PD) is aetiologically complex with both familial and sporadic forms. Familial PD results from rare, highly penetrant pathogenic mutations whereas multiple variants of low penetrance may contribute to the risk of sporadic PD. Comm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f04c3419ae543ffaecab7a827ab74af
https://doi.org/10.1016/j.parkreldis.2011.12.012
https://doi.org/10.1016/j.parkreldis.2011.12.012