Zobrazeno 1 - 10
of 169
pro vyhledávání: '"Jean Marc Burgunder"'
Autor:
Carsten Saft, Jean-Marc Burgunder, Matthias Dose, Hans Heinrich Jung, Regina Katzenschlager, Josef Priller, Huu Phuc Nguyen, Kathrin Reetz, Ralf Reilmann, Klaus Seppi, Georg Bernhard Landwehrmeyer
Publikováno v:
Neurological Research and Practice, Vol 5, Iss 1, Pp 1-11 (2023)
Abstract Introduction Choreiform movement disorders are characterized by involuntary, rapid, irregular, and unpredictable movements of the limbs, face, neck, and trunk. These movements often initially go unnoticed by the affected individuals and may
Externí odkaz:
https://doaj.org/article/d590a3c651f34c46a0ea9583802bc1bd
Autor:
Carsten Saft, Jean-Marc Burgunder, Matthias Dose, Hans Heinrich Jung, Regina Katzenschlager, Josef Priller, Huu Phuc Nguyen, Kathrin Reetz, Ralf Reilmann, Klaus Seppi, Georg Bernhard Landwehrmeyer
Publikováno v:
Neurological Research and Practice, Vol 5, Iss 1, Pp 1-10 (2023)
Abstract Introduction Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The pharmacological treatment of motor signs (e.g. chorea) may favorably or unfavorably impact other
Externí odkaz:
https://doaj.org/article/82e711d767b446e48816d7f63ace04bb
Autor:
Jie-Qiang Xia, Yang-Fan Cheng, Si-Rui Zhang, Yuan-Zheng Ma, Jia-Jia Fu, Tian-Mi Yang, Ling-Yu Zhang, Jean-Marc Burgunder, Hui-Fang Shang
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
ObjectivesThis study aims to elucidate the role of peripheral inflammation in Huntington’s disease (HD) by examining the correlation of peripheral inflammatory markers with clinical manifestations and disease prognosis.MethodsThis investigation inv
Externí odkaz:
https://doaj.org/article/75f6c4a4378c4a82a87ac5f8589a8901
Autor:
Yang‐Fan Cheng, Kun‐Cheng Liu, Tian‐Mi Yang, Yi Xiao, Qi‐Rui Jiang, Jing‐Xuan Huang, Sirui Zhang, Qian‐Qian Wei, Ru‐Wei Ou, Chun‐Yu Li, Xiao‐Jing Gu, Jean‐Marc Burgunder, Hui‐Fang Shang
Publikováno v:
Brain and Behavior, Vol 13, Iss 11, Pp n/a-n/a (2023)
Abstract Background and aim Huntington's disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CAG repeats expansion. Cognitive decline contributes to the loss of daily activity in manifest HD. We aimed to examine the c
Externí odkaz:
https://doaj.org/article/8b1ab19aa9d9438da3df0e48b49ceb15
Autor:
Quang Tuan Rémy Nguyen, Juan Dario Ortigoza Escobar, Jean-Marc Burgunder, Caterina Mariotti, Carsten Saft, Lena Elisabeth Hjermind, Katia Youssov, G. Bernhard Landwehrmeyer, Anne-Catherine Bachoud-Lévi
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/842b211e24b54b5584c216ade7a2699e
Autor:
Quang Tuan Rémy Nguyen, Juan Dario Ortigoza Escobar, Jean-Marc Burgunder, Caterina Mariotti, Carsten Saft, Lena Elisabeth Hjermind, Katia Youssov, G. Bernhard Landwehrmeyer, Anne-Catherine Bachoud-Lévi
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
One percent of patients with a Huntington's disease (HD) phenotype do not have the Huntington (HTT) gene mutation. These are known as HD phenocopies. Their diagnosis is still a challenge. Our objective is to provide a diagnostic approach to HD phenoc
Externí odkaz:
https://doaj.org/article/3011f0d891484295bcee2021ed3f5e98
Autor:
Huajing You, Tengteng Wu, Gang Du, Yue Huang, Yixuan Zeng, Lishan Lin, Dingbang Chen, Chao Wu, Xunhua Li, Jean-marc Burgunder, Zhong Pei
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Objective: Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder. Neurofilament light protein (NfL) is correlated with clinical severity of HD but relative data are the lack in the Chinese population. Reactive astrocytes are r
Externí odkaz:
https://doaj.org/article/7597e9b8b9594d0e9cd79cb62e077540
Autor:
Tobias Nef, Alvin Chesham, Narayan Schütz, Angela Amira Botros, Tim Vanbellingen, Jean-Marc Burgunder, Julia Müllner, René Martin Müri, Prabitha Urwyler
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
There is currently a need for engaging, user-friendly, and repeatable tasks for assessment of cognitive and motor function in aging and neurodegenerative diseases. This study evaluated the feasibility of a maze-like Numberlink puzzle game in assessin
Externí odkaz:
https://doaj.org/article/5f9eb4fbbc5b459cbe41e6f3db0532b3
Autor:
Xiao-Yan, Li, Yu-Feng, Bao, Juan-Juan, Xie, Shu-Xia, Qian, Bin, Gao, Miao, Xu, Yi, Dong, Jean-Marc, Burgunder, Zhi-Ying, Wu
Publikováno v:
Journal of Huntington's Disease. 11:407-413
Background: The Unified Huntington’s Disease Rating Scale (UHDRS) is a universal scale assessing disease severity of Huntington’s disease (HD). However, the English version cannot be widely used in China, and the reliability and validity of the C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65aa5cb8c84c93c221bf0811317da859
https://doi.org/10.3233/jhd-220542
https://doi.org/10.3233/jhd-220542
Autor:
Stefanie Kübel, Katharina Stegmayer, Tim Vanbellingen, Manuela Pastore-Wapp, Manuel Bertschi, Jean-Marc Burgunder, Eugenio Abela, Bruno Weder, Sebastian Walther, Stephan Bohlhalter
Publikováno v:
NeuroImage: Clinical, Vol 16, Iss , Pp 88-97 (2017)
Parkinson's disease (PD) patients frequently suffer from dexterous deficits impeding activities of daily living. There is controversy whether impaired fine motor skill may stem from limb kinetic apraxia (LKA) rather than bradykinesia. Based on classi
Externí odkaz:
https://doaj.org/article/a6733f837df747a8bf127e65d9d22a3c