Medicine & Life Sciences
Mutation
100%
Hereditary Spastic Paraplegia
81%
Mitochondrial Dynamics
60%
Myasthenia Gravis
50%
Steroids
48%
Nucleocapsid Proteins
41%
Congenital Myasthenic Syndromes
39%
Autosomal recessive 1 Spinocerebellar ataxia
36%
Fibroblasts
36%
Histidine-tRNA Ligase
35%
HIV Infections
35%
Phenotype
35%
Mitochondrial DNA
35%
Exome
34%
Biopsy
34%
Peripheral Nervous System Diseases
33%
Familial Dysautonomia
33%
Distal Myopathies
33%
Equine infectious anemia virus
31%
Neurons
31%
Rhodococcus equi
31%
Machado-Joseph Disease
30%
Myelin-Associated Glycoprotein
29%
Mitochondria
29%
Inclusion Body Myositis
29%
RNA-Directed DNA Polymerase
29%
Immune Reconstitution Inflammatory Syndrome
29%
HIV
28%
Genes
28%
Amino Acyl-tRNA Synthetases
27%
Progressive Multifocal Leukoencephalopathy
27%
Lysosomal Storage Diseases
27%
Proton Therapy
27%
Retroviridae
27%
Hypoventilation
26%
Brain Abscess
25%
Rhabdomyolysis
25%
Genetic Loci
24%
Missense Mutation
24%
Genetic Recombination
24%
Temporal Lobe Epilepsy
23%
N-Acetylneuraminic Acid
23%
Purkinje Cells
22%
Skeletal Muscle
22%
Cholinergic Receptors
22%
Skull Base
21%
Rituximab
21%
Sleep Apnea Syndromes
21%
Ribonuclease H
21%