The NOTCH2NLC gene 5′ untranslated region (UTR) GGC repeat expansion mutations
were identified as a genetic contributor of neuronal intranuclear inclusion disease (NIID) in …

Objective To summarize the reliable risk factors of impulsive-compulsive behaviors (ICBs) in
Parkinson’s disease (PD) patients through a meta-analysis on studies in which PD-ICBs …

Alpha-synucleinopathy is postulated to be central to both idiopathic rapid eye movement sleep
behaviour disorder (iRBD) and Parkinson’s disease (PD). Growing evidence suggests an …

Introduction: China has the most people with Parkinson disease (PD) in the world and is
estimated to have over half of the worldwide PD population. The objective of this study was to …

We read the recent paper by Sun et al.(2020) which showed that abnormal GGC repeat
expansion in the NOTCH2NLC gene with a detection rate of 5.58% was found in a cohort of …

Background Neuronal intranuclear inclusion disease (NIID) is a great imitator with a broad
spectrum of clinical manifestations that include dementia, parkinsonism, paroxysmal …

Background: Impulse control and related disorders (ICRDs) have gained recognition as a
severe complication of Parkinson's disease (PD) and are connected to poor quality of life and …

Introduction: China has the largest population of people with dementia in the world and is
estimated to have approximately a quarter of the entire population with dementia worldwide, …

Background Essential tremor (ET) is a neurological disease characterized by action tremor
in upper arms. Although its high heritability and prevalence worldwide, its etiology and …

Autosomal dominant sleep-related hypermotor epilepsy (ADSHE) is characterized by severe
sleep-related rigid hypermotor seizures. The pathogenic genes of ADSHE include genes …