Zobrazeno 1 - 10
of 199
pro vyhledávání: '"Jean‐Pierre Lin"'
Autor:
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, Nathalie Dorison, Serena Galosi, Giacomo Garone, Masa Malenica, Claudia Ravelli, Esra Serdaroglu, Laura A. van de Pol, Anne Koy, Vincenzo Leuzzi, Agathe Roubertie, Jean-Pierre Lin, Diane Doummar, Laura Cif, Juan Darío Ortigoza-Escobar
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundGNAO1-related disorders (GNAO1-RD) encompass a diverse spectrum of neurodevelopmental and movement disorders arising from variants in the GNAO1 gene. Dyskinetic crises, marked by sudden and intense exacerbations of abnormal involuntary move
Externí odkaz:
https://doaj.org/article/b868ccdbbf144a0ebf6daa05480378e6
Autor:
Jean-Pierre Lin
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/066f0e27a3004da68c78bbf9bd9a8d8b
Autor:
Verity M. McClelland, Jean-Pierre Lin
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Dystonia is a disorder of sensorimotor integration, involving dysfunction within the basal ganglia, cortex, cerebellum, or their inter-connections as part of the sensorimotor network. Some forms of dystonia are also characterized by maladaptive or ex
Externí odkaz:
https://doaj.org/article/cdf1aa027daa4e448bb8ed5087f6ad97
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Objective: To explore preliminary effectiveness of the Cognitive Orientation to daily Occupational Performance (CO-OP) Approach in improving outcomes in childhood-onset hyperkinetic movement disorders (HMDs) including dyskinetic cerebral palsy follow
Externí odkaz:
https://doaj.org/article/0dba5adf7e904f0c805874d46bb2eba6
Autor:
Verity M McClelland, Petra Fischer, Eleonora Foddai, Sofia Dall'Orso, Etienne Burdet, Peter Brown, Jean-Pierre Lin
Publikováno v:
NeuroImage: Clinical, Vol 30, Iss , Pp 102569- (2021)
Dystonia is a disorder of sensorimotor integration associated with abnormal oscillatory activity within the basal ganglia-thalamo-cortical networks. Event-related changes in spectral EEG activity reflect cortical processing but are sparsely investiga
Externí odkaz:
https://doaj.org/article/7ebf482b770e409796e335469813fbf5
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: While Deep Brain Stimulation (DBS) of the Globus pallidus internus is a well-established therapy for idiopathic/genetic dystonia, benefits for acquired dystonia are varied, ranging from modest improvement to deterioration. Predictive biom
Externí odkaz:
https://doaj.org/article/1a6b623751a042a9969631548fa7b50e
Autor:
Jean-Pierre Lin, Nardo Nardocci
Publikováno v:
Frontiers in Neurology, Vol 7 (2016)
Dystonia in childhood may be severely disabling and often un-remitting and un-recognised. Considered a rare disorder, dystonic symptoms in childhood are pervasive in many conditions including disorders of developmental delay, cerebral palsy, autism,
Externí odkaz:
https://doaj.org/article/62df3cfde9924422a808fb4b275d1bb7
Publikováno v:
Tremor and Other Hyperkinetic Movements, Vol 3 (2013)
Background: Sydenham's chorea (SC) is the most common type of acquired chorea in childhood. In some cases, symptoms (most commonly described in terms of neurological signs) last up to 2 years, and many cases relapse. This report describes the clinica
Externí odkaz:
https://doaj.org/article/0ca52e220148474491361278b6db5a41
Autor:
Tamara Pringsheim, Amit Batla, Ali Shalash, Jitendra Kumar Sahu, Carlos Cosentino, Darius Ebrahimi‐Fakhari, Jennifer Friedman, Jean‐Pierre Lin, Jonathan Mink, Alexander Munchau, Daniela Munoz, Nardo Nardocci, Belen Perez‐Dueñas, Zomer Sardar, Chahnez Triki, Hilla Ben‐Pazi, Laura Silveira‐Moriyama, Monica Troncoso‐Schifferli, Kyoko Hoshino, Russell C. Dale, Victor S.C. Fung, Manju A. Kurian, Emmanuel Roze
Publikováno v:
Scientia
Movement disorders: Pediatrics Trastornos del movimiento; Pediatría Trastorns del moviment; Pediatria Background The International Parkinson and Movement Disorders Society (MDS) set up a working group on pediatric movement disorders (MDS Task Force
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f08ed9f4656ceb2a51243c736588d1d8
https://doi.org/10.1002/mdc3.13728
https://doi.org/10.1002/mdc3.13728
Autor:
Nicholas M Allen, Mark O’Rahelly, Bruno Eymard, Mondher Chouchane, Andreas Hahn, Gerry Kearns, Dae-Seong Kim, Shin Yun Byun, Cam-Tu Emilie Nguyen, Ulrike Schara-Schmidt, Heike Kölbel, Adela Della Marina, Christiane Schneider-Gold, Kathryn Roefke, Andrea Thieme, Peter Van den Bergh, Gloria Avalos, Rodrigo Álvarez-Velasco, Daniel Natera-de Benito, Man Hin Mark Cheng, Wing Ki Chan, Hoi Shan Wan, Mary Ann Thomas, Lauren Borch, Julie Lauzon, Cornelia Kornblum, Jens Reimann, Andreas Mueller, Thierry Kuntzer, Fiona Norwood, Sithara Ramdas, Leslie W Jacobson, Xiaobo Jie, Miguel A Fernandez-Garcia, Elizabeth Wraige, Ming Lim, Jean Pierre Lin, Kristl G Claeys, Selma Aktas, Maryam Oskoui, Yael Hacohen, Ameneh Masud, M Isabel Leite, Jacqueline Palace, Darryl De Vivo, Angela Vincent, Heinz Jungbluth
Publikováno v:
Brain.
In utero exposure to maternal antibodies targeting the fetal acetylcholine receptor isoform (fAChR) can impair fetal movement, leading to arthrogryposis multiplex congenita (AMC). fAChR antibodies have also been implicated in apparently rare, milder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34284e62cb5632e5fa3d1b50598045eb
https://doi.org/10.1093/brain/awad153
https://doi.org/10.1093/brain/awad153