Results 231 to 240 of about 128,425 (312)

Efficacy of IncobotulinumtoxinA (BoNT‐A) Injections in Upper Limb Task‐Specific and Position‐Dependent Tremors

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Task‐specific tremors (TST) and position‐dependent tremors (PDT) are rare isolated focal tremors that impair fine motor control with few effective treatment options. Although botulinum neurotoxin (BoNT) is effective in other tremor syndromes, its evidence in these tremor subtypes remains limited.
Elizabeth K. Boyd, Shangge Jiang, Runjie Bill Shi, Philippe Rizek   +3 more
wiley   +1 more source

Computational Modeling of Sequential Dependencies in Mother-Child Social Interaction and Associations to Empathic Responses. [PDF]

Dev Sci
Nunez E, Minagawa Y, Hirokawa M, Yamamoto E, Hakuno Y, Suzuki K.   +5 more
europepmc   +1 more source

Presynaptic Congenital Myasthenic Syndromes

Muscle &Nerve, EarlyView.
ABSTRACT Presynaptic congenital myasthenic syndromes (CMS) encompass a large number of rare neurologic disorders caused by impaired release of acetylcholine (ACh) from motor nerve terminals. There are two main groups of presynaptic CMS: one in which the amount of ACh in synaptic vesicles (SV) is diminished and another in which the mechanism of synaptic
Ricardo A. Maselli
wiley   +1 more source

Exploring EMG Biofeedback in Core Training - Bosu Ball vs Swiss Ball Efficacy for Collegiate Students with Mechanical Low Back Pain: A Randomized Controlled Trial. [PDF]

J Multidiscip Healthc
Khanduri A, Sharma P, Malhotra N, Aggarwal D, Ahmad I, Iqbal ZA, Alshehri MM, Sahely A, Shaphe MA, Aldhahi MI.   +9 more
europepmc   +1 more source

The Differing Phenotypes of the Three Most Common Postsynaptic Congenital Myasthenic Syndromes Governed by Their Underlying Molecular Pathogenic Mechanisms

Muscle &Nerve, EarlyView.
ABSTRACT The congenital myasthenic syndromes are rare disorders of impaired signal transmission at the neuromuscular junction. Despite next generation sequencing facilitating the identification of variants in myasthenic‐associated genes, these variants are frequently of unknown significance and the clinical diagnosis can be delayed.
David Beeson
wiley   +1 more source

Clinical value and advances of electromyography in cervical dystonia: a review. [PDF]

Front Neurol
Bao M, Ma D, Zhou M, Ma X, Sun H, Zhu L, Hou S, Meng H.   +7 more
europepmc   +1 more source

Clinical Characteristics and Treatment Management of Seronegative Myasthenia Gravis: A Systematic Review of the Literature

Muscle &Nerve, EarlyView.
ABSTRACT Seronegative myasthenia gravis (SNMG) is characterized by the absence of detectable autoantibodies against known MG targets, despite clinical and electrophysiological evidence of a postsynaptic neuromuscular junction disorder. The aim of this systematic review was to better define clinical features, diagnostic clues and treatment outcome of ...
Massimiliano Ugo Verza, Mattia Schiavolin, Francesca Beretta, Sara Cornacchini, Antonio Lotti, Gregorio Spagni, Valentina Damato   +6 more
wiley   +1 more source

Surface EMG for Force Control of Mechanical Hands

, 2008
Hirzinger, Gerd, Claudio Castellini, Patrick van der Smagt, P. V. der Smagt, C. Castellini, Castellini, Claudio, Giulio Sandini, Gerd Hirzinger, G. Hirzinger, Smagt van der, Patrick, Sandini, Giulio   +10 more
core   +1 more source

High-Density EEG and Multi-Muscle EMG Dataset during Object Prehension with a sensorized Grasping Box in Humans. [PDF]

Sci Data
Lomele G, Lencioni T, D'Ambrosio S, Comanducci A, Lucchetti F, Marzegan A, Derchi C, Garzonio S, Atzori T, Rabuffetti M, Castiglioni P, Ferrarin M, Fornia L.   +12 more
europepmc   +1 more source

Functional Sneeze: A Case Report

Movement Disorders Clinical Practice, EarlyView.
Alexandra Lodge, Barnaby J. Proctor, Jan Coebergh   +2 more
wiley   +1 more source