Results 251 to 260 of about 81,579 (355)

Abnormal Connectivity of the Head Neural Integrator in Cervical Dystonia

Movement Disorders, EarlyView.
Abstract Background Cervical dystonia is characterized by abnormal neck and head movements, possibly related to a dysfunction of the interstitial nucleus of Cajal (INC) and the head neural integrator, a system responsible for the control of head and eye movements.
Giuseppe A. Zito, Emmanuel Roze, Clément Tarrano, Salim Ouarab, Prasanthi Jegatheesan, Asya Ekmen, Benoît Béranger, Romain Valabregue, Cécile Hubsch, Sophie Sangla, Cécilia Bonnet, Cécile Delorme, Aurélie Méneret, Bertrand Degos, Floriane Bouquet, Marion Apoil Brissard, Marie Vidailhet, Dominique Hasboun, Pierre Pouget, Yulia Worbe, Cécile Gallea   +20 more
wiley   +1 more source

Deep Phenotyping of Musicians' Upper Limb Dystonia. [PDF]

Tremor Other Hyperkinet Mov (N Y)
Frucht SJ.
europepmc   +1 more source

Plasma Markers of Astrocytic and Axonal Integrity in Idiopathic/Isolated REM Sleep Behavior Disorder (iRBD) as Predictors of Dementia with Lewy Bodies

Movement Disorders, EarlyView.
Abstract Background Plasma biomarkers of neurodegeneration, astrogliosis, and neuroinflammation have been studied as potential biomarkers in neurodegenerative diseases. This study investigated whether these markers may predict phenoconversion to Parkinson's disease or dementia with Lewy bodies (DLB) in idiopathic/isolated REM sleep behavior disorder ...
Aline Delva, Cinzia Zatti, Amélie Pelletier, Jacques Montplaisir, Jean‐François Gagnon, Gwendlyn Kollmorgen, Tony Kam‐Thong, Thomas Kustermann, Venissa Machado, Ronald B. Postuma   +9 more
wiley   +1 more source

Spinocerebellar ataxias masquerading as movement disorders: clinical and genetic characterization. [PDF]

Front Neurol
Wei S, Zhao Z, Li N, Guo X, Chen J, Hu J.   +5 more
europepmc   +1 more source

Somato‐Cognitive Action Network in Focal Dystonia

Movement Disorders, EarlyView.
Abstract Background The central pathology causing idiopathic focal dystonia remains unclear. The recently identified somato‐cognitive action network (SCAN) has been implicated. Objective We tested whether the effector‐agnostic SCAN may constitute a central pathology shared across dystonia subtypes, whereas the effector‐specific regions in the primary ...
Yuchao Wang, Baothy Huynh, Jianxun Ren, Mo Chen, Wei Zhang, Dan Hu, Shasha Li, Hesheng Liu, Teresa J. Kimberley   +8 more
wiley   +1 more source

Drinking Tremor

Movement Disorders Clinical Practice, EarlyView.
Victor Rebelo Procaci, Lyamara Apostólico de Azevedo, Orlando Graziani Povoas Barsottini, Henrique Ballalai Ferraz, José Luiz Pedroso   +4 more
wiley   +1 more source

Paroxysmal Dystonia: An Etiology Not to Be Missed in an Older Adult Patient

Movement Disorders Clinical Practice, EarlyView.
Valentin Mira, Jan Patrick Stellman, Stephan Grimaldi   +2 more
wiley   +1 more source

Compound Heterozygous Structural Variants in Cases with Unsolved PRKN‐Associated Parkinson's Disease

Movement Disorders, EarlyView.
Abstract Background Biallelic mutations in the PRKN gene are a common cause of early‐onset Parkinson's disease (EOPD). In addition to single nucleotide variants, structural variants contribute substantially to the mutational profile of PRKN. A significant portion of patients with EOPD remains genetically unsolved.
Agata Fant, Sara Trova, Edoardo Monfrini, Gaia Treves, Francesco Musacchia, Fabio Landuzzi, Paola Mandich, Antonio Amoroso, Remo Sanges, Luca Pandolfini, Francesco Cavallieri, Franco Valzania, Valentina Fioravanti, Giulia Di Rauso, Gloria Brescia, Enza Maria Valente, Valeria Tiranti, Luigi Michele Romito, Chiara Reale, Barbara Garavaglia, Antonio Emanuele Elia, Andrea Cavalli, Alessio Di Fonzo, Manuela Vecchi, Stefano Gustincich   +24 more
wiley   +1 more source

A Novel α‐Synuclein K58N Missense Variant in a Patient with Parkinson's Disease

Movement Disorders, EarlyView.
Abstract Background Parkinson's disease (PD) is a complex multifactorial disorder with a genetic component in about 15% of cases. Multiplications and point mutations in SNCA gene, encoding α‐synuclein (aSyn), are linked to rare familial forms of PD. Objective Our goal was to assess the clinical presentation and the biological effects of a novel K58N ...
Mohammed Al‐Azzani, Sandrina Weber, Nagendran Ramalingam, Maria Ramón, Liana Shvachiy, Gonçalo Mestre, Michael Zech, Kevin Sicking, Alain Ibáñez de Opakua, Vidyashree Jayanthi, Leslie Amaral, Aishwarya Agarwal, Aswathy Chandran, Susana R. Chaves, Juliane Winkelmann, Claudia Trenkwalder, Maike Schwager, Silke Pauli, Ulf Dettmer, Claudio O. Fernández, Janin Lautenschläger, Markus Zweckstetter, Ruben Fernandez‐Busnadiego, Brit Mollenhauer, Tiago Fleming Outeiro   +24 more
wiley   +1 more source

Treatment of Primary Cranial Dystonia (Meige's Syndrome) With Clozapine

, 2000
Angelika Sieche, H. Giedke
openalex   +2 more sources