Medicine & Life Sciences
Multiple System Atrophy
100%
Autopsy
63%
Olivopontocerebellar Atrophies
60%
Striatonigral Degeneration
43%
Chromosomes, Human, Pair 3
33%
Neurons
23%
Cerebellum
23%
Primary Dysautonomias
18%
Chromosomes, Human, Pair 8
17%
Chromosomes, Human, Pair 4
16%
Cerebellar Diseases
16%
Cerebellar Nuclei
16%
Cerebellar Ataxia
15%
alpha-Synuclein
15%
Inclusion Bodies
14%
Zinc Fingers
14%
Parkinsonian Disorders
13%
Genome-Wide Association Study
13%
Diagnostic Errors
12%
Rare Diseases
12%
Genetic Variation
12%
Frontal Lobe
11%
Autoantibodies
11%
Neuroglia
11%
Neurodegenerative Diseases
10%
Single Nucleotide Polymorphism
10%
Inpatients
10%
Mutation
7%
Brain
6%
Genes
5%
Proteins
4%