Results 171 to 180 of about 263,206 (355)

Effects of Pallidal Deep Brain Stimulation on Speech and Swallowing in Pediatric Patients with Dystonia

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Bilateral globus pallidus internus deep brain stimulation (GPi‐DBS) is a proven safe and effective treatment in certain forms of idiopathic or inherited dystonia (ID/IN). Its effects in acquired dystonia such as in dyskinetic cerebral palsy (DCP) however vary widely.
Katerina Bernardi, Andrea A. Kühn, Ana Luísa de Almeida Marcelino, Matthias Eckenweiler, Cornelia Rensing‐Zimmermann, Joachim K. Krauss, Joachim Runge, Rene Marquez Franco, Delia Lorenz, Monika Müller, Alfons Schnitzler, Andrea Bevot, Lidwin von Spee, Veerle Visser‐Vandewalle, Lars Timmermann, Petra Schiller, Anne Koy   +16 more
wiley   +1 more source

Early detection of Australian Aboriginal and Torres Strait Islander infants at high risk of adverse neurodevelopmental outcomes at 12 months corrected age: LEAP-CP prospective cohort study protocol

BMJ Open, 2022
Robert S Ware, Roslyn N Boyd, Arend F Bos, Katherine Benfer, Natasha Reid, Carly R Luke, Leeann Mick-Ramsamy, Margot Bosanquet   +7 more
doaj   +1 more source

Complementary and Integrative Medicine for the Treatment of Tourette's Syndrome

Movement Disorders Clinical Practice, EarlyView.
Abstract Background There is widespread interest in complementary and integrative medicine (CIM) among people with Tourette's syndrome (TS). Objective To perform a systematic review of evidence on the use of CIM to reduce tics and improve tic‐related quality of life.
Tamara Pringsheim, Catherine Deans, Saar Anis, Poonam Bhatia, Kevin Black, Yildiz Degirmenci, Donald Gilbert, Andreas Hartmann, Mariam Hull, Irene Malaty, Davide Martino, Alex Medina Escobar, Pablo Mir, Christelle Nilles, Marianna Sarchioto, Jibrin Sammani Usman, Harini Sarva, Katarzyna Smilowksa, Natalia Szejko, Kinga Tomczak, Daniel van Wamelen, Yulia Worbe   +21 more
wiley   +1 more source

The use of botulinum toxin A in children with cerebral palsy, with a focus on the lower limb [PDF]

, 2010
Guy Molenaers, Anja Van Campenhout, Katrien Fagard, Jos De Cat, Kaat Desloovere   +4 more
openalex   +1 more source

The Spectrum of Abnormal Tongue Movements: Review of Phenomenology, Etiology, and Differential Diagnosis

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Classifying abnormal tongue movements is challenging due to their varied presentations and limited visibility compared to other body parts. Accurate identification of the phenomenology guides physical examination and can point to specific diagnoses.
Nathaniel Bendahan, Seyed‐Mohammad Fereshtehnejad, Christos Ganos, Emily Swinkin, Anthony E. Lang   +4 more
wiley   +1 more source

Gastrostomy feeding in cerebral palsy: enough and no more [PDF]

, 2010
Angharad Vernon‐Roberts, Jonathan C. K. Wells, Hugh W. Grant, Nicola Alder, Babu Vadamalayan, Muftah Eltumi, Peter Sullivan   +6 more
openalex   +1 more source

A Biomarker‐Based Classification of Corticobasal Syndrome

Movement Disorders, EarlyView.
Abstract Background Corticobasal syndrome (CBS) is a clinically defined syndrome with progressive movement and cortical dysfunction, caused by various underlying pathologies, most commonly tau‐predominant pathologies such as progressive supranuclear palsy and corticobasal degeneration, or Alzheimer's disease (AD).
Carla Palleis, Alexander Maximilian Bernhardt, Endy Weidinger, Urban M. Fietzek, Alexander Jäck, Sabrina Katzdobler, Johannes Gnörich, Theresa Bauer, Nicolai Franzmeier, Robert Perneczky, German Imaging Initiative for Tauopathies (GII4T), Matthias Brendel, Johannes Levin, Günter U. Höglinger   +13 more
wiley   +1 more source

Cerebral Palsy: Motor Types, Gross Motor Function and Associated Disorders [PDF]

, 2011
Farin Soleimani, Roshanak Vameghi, Mehdi Rassafiani, Nazila Akbar Fahimi, Zahra Nobakht   +4 more
openalex  

Integrating Long‐Read Nanopore Sequencing for Precision Resolution of Genomic Variants in Dystonia

Movement Disorders, EarlyView.
Abstract Background Although many individuals with dystonia present with features indicative of single‐gene etiologies, obtaining definitive genetic diagnoses can be challenging. Objective We assessed the value of nanopore‐based long‐read sequencing (LRS) in achieving molecular clarification of dystonic syndromes.
Ugo Sorrentino, Martin Pavlov, Nazanin Mirza‐Schreiber, Melanie Brugger, Theresa Brunet, Eugenia Tsoma, Alice Saparov, Ivana Dzinovic, Philip Harrer, Antonia M. Stehr, Matias Wagner, Erik Tilch, Barbara Wallacher, Shiraz Alhasan, Anne Koy, Alessio Di Fonzo, Miriam Kolnikova, Katarina Kusikova, Petra Havrankova, Raushana Tautanova, Sandy Lösecke, Sebastian Eck, Sylvia Boesch, Jan Necpal, Matej Skorvanek, Robert Jech, Holger Prokisch, Juliane Winkelmann, Konrad Oexle, Elisabeth Graf, Michael Zech   +30 more
wiley   +1 more source

Extrapolating published survival curves to obtain evidence‐based estimates of life expectancy in cerebral palsy [PDF]

, 2015
Steven M. Day, Robert J. Reynolds, Scott J. Kush   +2 more
openalex   +1 more source