Abstract The ILAE's Task Force on Nosology and Definitions revised in 2022 its definition of
juvenile myoclonic epilepsy (JME), the most common idiopathic generalized epilepsy …

Abstract Functional Motor Disorders are common and disabling. Clinical diagnosis has
moved from one of exclusion of other causes for symptoms to one where positive clinical …

Introduction Negative myoclonus (NM) is an involuntary movement caused by a sudden
interruption of muscular activity, resulting in gait problems and falls. Objective To establish …

Progressive myoclonus ataxia (PMA) is a rare clinical syndrome characterized by the
presence of progressive myoclonus and ataxia, and can be accompanied by mild cognitive …

The duration of slow-wave sleep (SWS) is related to the reported sleep quality and to the
important variables of mental and physical health. The internal cues to end an episode of …

This study presents a novel approach utilizing solvothermal techniques to synthesize zeolitic
imidazolate framework (ZIF‐4) particles. Various properties of the ZIF‐4 particles are …

Stiff-person syndrome is rare and disabling autoimmune condition that most frequently
affects women, with no real predisposition by race. Diagnosis is often arduous, which is why …

Myoclonus-Dystonia is a rare, neurological movement disorder, clinically characterized by
myoclonic jerks and dystonic symptoms, such as cervical dystonia and writer's cramp …

Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in ARHGEF9
Deficiency Neurophysiological Analysis of Cortical Myoclonic Tremor and Excessive Startle in …

Secondary movement disorders (SMDs) represent a heterogeneous group of neurological
conditions characterized by abnormal, involuntary movements resulting from various …