A Long-Living Human Tissue Engineered Nigrostriatal Pathway as a Testbed to Study Parkinson’s Disease
Objective: To create a three dimensional (3D) long-living model of human tissue-engineered nigrostriatal pathway (TE-NSP) comprised of discrete somatic and axonal compartments recapitulating the native…Predictors of Рostural Instability and Gait Disturbances after STN-DBS in Parkinson’s Disease
Objective: The aim was to identify characteristic pre-surgical visual and vestibular disturbances, as well as neuroimaging changes that could be predictors of PI and gait…Differentiating Parkinsonism and related diseases by specific Parkinsonism patterns
Objective: This study aimed to identify characteristic parkinsonism patterns across PD, MSA and PSP, and evaluate their utility in early differentiation. Background: Parkinson's disease (PD), multiple…Transcranial sonography in Parkinson’s disease patients
Objective: To present the usage and results of transcranial sonography (TCS) in Parkinson's disease (PD) patients. Background: (TCS) has emerged as a valuable diagnostic tool…Multiparametric Prediction of Mild Cognitive Impairment in Parkinson’s Disease Using a Combination of Structural and Functional MRI Measures
Objective: To investigate whether the multiparametric combination of structural and functional (fMRI) neuroimaging parameters improves the prediction of mild cognitive impairment (MCI) in Parkinson's disease…Clinical And Cerebellar Structural Alterations In Parkinson’s Disease Patients With Freezing Of Gait
Objective: To assess clinical and cerebellar volume differences in Parkinson’s disease (PD) patients with and without freezing of gait (PD-FoG and PD-NOFoG). Background: Cerebellum plays…Novel Parkinson’s Disease Genetic Risk Factors Within and Across European Populations
Objective: To assess genome-wide genetic risk for Parkinson’s disease (PD) within and across genetically determined European ancestries (European, Ashkenazi Jewish, Finnish, and Icelandic). We conducted…Analysis showed resemblance in Genetic architecture of rare movement disorders in consanguineous Pashtoon ethnic group
Objective: Present Study was focused on improving the available genetic architecture of rare movement disorders (MD) and subsequent use of this knowledge for protective measurements…Non-motor Symptoms, Sleep Disturbances, And Genetic Insights In Young Onset Parkinson’s Disease: A Prospective Descriptive Study
Objective: 1. To study the prevalence of various non-motor symptoms in Young onset Parkinson's Disease patients2. To study the genetic markers in YOPD patients. Background:…Gene Polymorphisms of Parkinson’s Disease risk locus and idiopathic REM Sleep Behavior Disorder
Objective: Genetic factors play an important role in idiopathic rapid eye movement sleep behavior disorder (iRBD) but have not been fully studied. Background: This study…
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