Rotenone and Parkinson’s disease (PD): Effect modification by membrane transporter variants
Objective: Determine whether variants in the xenobiotic efflux membrane transporter p-glycoprotein gene (ABCB1, p-gp, MDR1) modify the association of rotenone and PD. Background: Use of…Impact of pre- and postdiagnosis physical activity on the progression of Parkinson’s disease
Objective: To assess whether and how pre- and postdiagnosis physical activities affect motor function, cognition, and depression among Parkinson's disease (PD) patients. Background: Physical activities…Do-not-resuscitate utilization in inpatient Parkinson’s disease in the United States
Objective: To investigate Do-not-resuscitate (DNR) order utilization in Parkinson's disease (PD) hospitalizations patients in the United States. Background: DNR order utilization in PD has been…Assessment of malnutrition in patients with Parkinson’s disease
Objective: We aimed to assess malnutrition and those at risk of malnutrition in PD patients with an age matched control group using the mini nutritional…The effect of a structured medication review on quality of life in patients with Parkinson’s disease. An interim analysis
Objective: To investigate whether a structured medication review executed by a community pharmacist improves medication adherence and influences quality of life in patients with Parkinson's…Wrist reveals the fall risk in activities of daily living
Objective: The focus of our cross-sectional study is on investigation of complex measures in terms of the fall risk (FR). The assessment was performed with…A 12-month, 2-arm, 2-period, randomized, controlled trial of a digital solution for the management of Parkinson’s disease (PD): Rationale and study design
Objective: To collect evidence to support the use of a digital solution to improve health outcomes in PD through remote, timely and appropriate drug adjustments,…Novel THAP1 missense mutation leading to focal and segmental dystonia
Objective: We have identified a novel heterozygous missense mutation in THAP1 (DYT6 locus) in a patient suffering from craniocervical and upper limb dystonia. We describe…Familial SPG17/distal hereditary motor neuropathy type V– Complicated hereditary spastic paraplegia with many faces
Objective: We present the clinical and genetic results of a SPG17 family with a vast intrafamilial phenotype from subclinical signs to a severe and rapidly…Reduced thalamo-cortical functional connectivity in asymptomatic LRRK2 mutation carriers
Objective: To characterize MRI functional patterns during resting state in asymptomatic LRRK2 mutation carriers. Background: Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are…
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