Medicine & Life Sciences
Parkinsonian Disorders
74%
Mutation
60%
Frontotemporal Dementia
58%
Progressive Supranuclear Palsy
30%
Genes
28%
Synucleins
27%
Frontotemporal Lobar Degeneration
25%
Dementia
24%
Pathology
20%
Multiple System Atrophy
20%
Leukoencephalopathies
19%
Chromosomes, Human, Pair 17
19%
Perry Syndrome
18%
Microtubule-Associated Proteins
18%
Leucine
18%
Neurodegenerative Diseases
18%
Alzheimer Disease
17%
Substantia Nigra
17%
Colony-Stimulating Factor Receptors
16%
Essential Tremor
16%
Phosphotransferases
16%
Lewy Bodies
16%
Brain
15%
Tremor
15%
Age of Onset
14%
Macrophage Colony-Stimulating Factor
13%
Atrophy
12%
Tauopathies
12%
Levodopa
12%
Phenotype
11%
Progranulins
11%
Genome-Wide Association Study
11%
Autopsy
11%
Neuroglia
10%
Haplotypes
10%
Amyotrophic Lateral Sclerosis
9%
Inborn Genetic Diseases
9%
Dystonia
9%
Exons
9%
Single Nucleotide Polymorphism
9%
White Matter
9%
Parkinson Disease, Familial, Type 1
8%
Alleles
8%
Frontotemporal Dementia With Motor Neuron Disease
7%
Ubiquitin
7%
Pallidopontonigral Degeneration
7%
Dystonic Disorders
7%