Keyphrases
Genotype-phenotype Correlation
75%
Cortical Dysfunction
50%
A53T
50%
Phenotypic Spectrum
50%
Genetic Testing
50%
Dystonia
50%
Dementia with Lewy Bodies
50%
Cocaine and Amphetamine Regulated Transcript
50%
Transthyretin
50%
Cerebrospinal Fluid Biomarkers
50%
Alzheimer's Dementia
50%
Body Effect
50%
Mutation Spectrum
50%
Disease Progression
50%
Prion Transmission
50%
GC Gene
50%
Gerstmann Syndrome
50%
Protein Kinase
50%
Slowly Progressive
40%
PSEN2
37%
Autosomal Dominant
37%
Autosomal Recessive Cerebellar Ataxia
30%
Gene mutation
30%
Presenilin 2
25%
Greek Americans
25%
CSF Biomarkers
25%
EEG Biomarker
25%
Autosomal Recessive Parkinsonism
25%
Levodopa-responsive
25%
American Family
25%
Dysphasia
25%
Presenilin
25%
Pathogenic mutations
22%
Ataxia
20%
Complex Phenotypes
20%
Neuroscience
Dementia with Lewy Body
100%
Dystonia
50%
Spinocerebellar Ataxia
50%
Cocaine and Amphetamine Regulated Transcript
50%
Transthyretin
50%
Ataxia
50%
Alzheimer's Disease
50%
calcium activated,phospholipid dependent protein kinase
41%
Presenilin 2
25%
Dysphasia
25%
Gene Mutation
25%
Polyglutamine
16%
Myoclonus
16%
Biochemistry, Genetics and Molecular Biology
Prion Protein
50%
Autosomal Dominant Inheritance
50%
PSEN2
50%
Genetic Screening
50%
Microchimerism
50%
Creutzfeldt-Jakob Disease
50%
Genotype Phenotype Correlation
33%
PSEN1
33%
Single Photon Emission Computed Tomography
25%
Denaturing High Performance Liquid Chromatography
16%
Chromosome 17
16%
Multiplex Ligation-Dependent Probe Amplification
16%
