Objective measurement of limb bradykinesia using marker-less tracking algorithm with 2D-video of PD patients
Objective: To objectively analyze motor symptoms with 2D RGB videos, which are easily accessible, attachment free and cost-effective. Background: Quantitative measurement of parkinsonian symptoms is…Arm Swing Differences in Patients with PD and ET during Walking
Objective: To identify objective biomarkers to improve clinical phenotyping and differential diagnosis in patients with PD and ET using wearable sensors. Background: At present, the…Positional variability in upper limb tremor in both essential and dystonic tremor: A case series
Objective: Characterize the positionality of upper limb tremor in clinical practice. Background: The MDS tasks force on tremor defines tremor as an involuntary, rhythmic, oscillatory…Quantitative study of the effect of thalamotomy by MRgFUS in the different types and locations of tremor in the contralateral upper limb
Objective: To quantify the improvement of different types of tremor in upper limb using the spectrum of accelerometer signal in patients treated with unilateral lesions…Use of Botulinum Toxin: Experience in a Cohort of Essential Tremor Patients
Objective: To review the treatment characteristics of botulinum toxin in medically refractory essential tremor (ET). Background: Treatment of medically refractory essential tremor has remained challenging…Physiotherapy: Functionality and Cognition in Parkinson’s Disease
Objective: This study aimed to investigate if there is any association between physical activity score and cognitive impairment in people with Parkinson’s disease (PD). Background:…Reclassification of variant c.5825C>T and clinical evidence of variant c.3955_3958dup in a Peruvian family with ATM syndrome
Objective: To describe a Peruvian family carrying variants c.3955_3958dup and c.5825C>T in the ATM gene. Background: Pathogenic variants at ATM gene are associated both, to…Clinical characterization and disease progression in spinocerebellar ataxia type 35: A case series
Objective: To characterize the clinical presentation and disease progression of patients with spinocerebellar ataxia type 35 (SCA35). Background: Mutations in TGM6 have been identified to…Clinical correlation with the Genotype of Friedreich’s Ataxia (FRDA) patients in Indian population
Objective: To describe genotype-phenotype correlation in Indian FRDA patients. Background: Friedreich’s Ataxia(FRDA), an early onset rare autosomal recessive ataxia is caused by bi-allelic loss of…Real-World Deutetrabenazine Dosing Patterns in Patients With Huntington’s Disease or Tardive Dyskinesia
Objective: To evaluate real-world treatment patterns and adherence to deutetrabenazine (DTBZ) in patients with Huntington’s disease (HD) or tardive dyskinesia (TD). Background: DTBZ is a…
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