Slow Motion Analysis of Repetitive Tapping (SMART) test: a new means to assess bradykinesia
Objective: To develop a quantitative and objective tool to track repetitive tapping movement (RTM) using a slow motion capture and compare patients with Parkinson’s disease…Utility of deep brain stimulation remote programming for Parkinson’s disease during the COVID-19 outbreak
Objective: Deep Brain Stimulation（DBS）tele-programming technique has been available for several years in China, which mainly served as a complementary approach to routine DBS treatment and…Deep brain stimulation revision from VIM to VIM and PSA severe long-standing refractory ET: case series
Objective: To describe 5 patients with ET who underwent replacement of VIM DBS with leads targeting both VIM and the posterior subthalamic area (PSA) due…Safety and efficacy of focused ultrasound staged bilateral thalamotomy for Essential tremor
Objective: To report preliminary results on the safety and efficacy of staged bilateral magnetic resonance-guided focused ultrasound (MRgFUS) thalamotomy for the treatment of essential tremor…‘Listen’ to your tremor patient..with a stethoscope!
Objective: To report a novel and inexpensive method for evaluating tremor in the clinic and at the bedside. Background: Tremor is the most common involuntary…Feasibility and Acceptability of Lee Silverman Voice Treatment for patients with hereditary ataxia
Objective: This study aimed to assess the feasibility and acceptability of Lee Silverman Voice Treatment (LSVT) provided via Skype for patients with hereditary ataxia. Background:…New pathogenic mutation in the Niemann-Pick C (NPC) Type 1 gene: Confirmation by diagnostic workup of NPC in a 41-year-old woman with idiopathic late onset cerebellar ataxia (ILOCA)
Objective: We present an instructive case of a 41-year-old woman with idiopathic late onset cerebellar ataxia. Background: Identifying the cause of idiopathic late onset cerebellar…Downbeat nystagmus and progressive ataxia mimicking a neurodegenerative disease: a specific phenotype of Chiari malformation
Objective: Case Report. Background: Chiari malformation type 1 (CM1) is a congenital neurological disease with posterior fossa hypoplasia and the cerebellar tonsils being forced through…Gerstmann-Sträussler-Scheinker disease presenting as a late onset slowly progressive spinocerebellar ataxia: expanding the phenotypic spectrum of genetic prion disease
Objective: We describe a late-onset presentation of Gerstmann-Sträussler-Scheinker disease (GSS) with a novel mutation in the prion protein (PRNP) gene. We compare this case to…The Impact of Antipsychotic Dose Reduction Within a Medicare Population
Objective: To analyze the burden of antipsychotic (AP) dose reduction in Medicare patients with schizophrenia (SZ). Background: Tardive dyskinesia (TD) develops in patients treated with…
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