Association of MAPT subhaplotypes with clinical and demographic features in Parkinson’s disease

Keyphrases

• Parkinson's Disease 100%
• Clinical Features 100%
• Demographic Characteristics 100%
• Age of Onset 40%
• Idiopathic Rapid Eye Movement Sleep Behavior Disorder (iRBD) 40%
• Restless Legs Syndrome 40%
• Dementia 20%
• Mayo Clinic 20%
• Risk Association 20%
• Disease Progression 20%
• Phenotypic Variation 20%
• Movement Disorders 20%
• Association Signal 20%
• Microtubule-associated Protein tau 20%
• Patients with Parkinson's Disease 20%
• Retrospective Cohort Study 20%
• Florida 20%
• Autonomic Dysfunction 20%
• Primary Outcome Measure 20%
• Dystonia 20%
• Motor Signs 20%
• Dyskinesia 20%
• Bradykinesia 20%
• Rest Tremor 20%
• Orthostatic Hypotension 20%
• Impulse Control Disorders 20%
• Parkinson's Disease Subtypes 20%
• Caucasian Patients 20%
• H2 Haplotype 20%
• Psychotic Features 20%
• Parkinson's Disease Risk 20%
• Haplotype Structure 20%

Neuroscience

• Parkinson's Disease 100%
• Rapid Eye Movement Sleep 28%
• Behavior Disorder 28%
• Haplotype 28%
• Restless Legs Syndrome 28%
• Tau Protein 14%
• Tremor 14%
• Stereotypic Movement Disorder 14%
• Mental Disorder 14%
• Dysautonomia 14%
• Dystonia 14%
• Impulse Control Disorder 14%
• Dyskinesia 14%
• Bradykinesia 14%