Medicine & Life Sciences
Limb-Girdle Muscular Dystrophies
100%
Duchenne Muscular Dystrophy
86%
Muscular Diseases
60%
Exons
47%
Dystrophin
43%
Mutation
42%
Myositis
40%
Muscular Dystrophies
39%
Muscles
33%
Dermatomyositis
30%
6-methylpurine
27%
Protein Isoforms
23%
Camptocormia
23%
Adenine Phosphoribosyltransferase
22%
Valosin Containing Protein
21%
Missense Mutation
19%
Myotonia Congenita
19%
Dystroglycans
19%
Tetrahymena
19%
Internal Ribosome Entry Sites
19%
Skeletal Muscle Fibers
18%
Exome
18%
Lithium Chloride
18%
5'-Nucleotidase
17%
Inclusion Body Myositis
17%
Antisense Oligonucleotides
15%
Therapeutics
15%
Antisynthetase syndrome
14%
Natural History
13%
Ophthalmoplegia
13%
Muscle Weakness
13%
Vacuoles
13%
Proteins
12%
Respiratory Insufficiency
12%
Phenotype
12%
Genetic Therapy
12%
Clinical Trials
10%
Registries
10%
Cell Line
9%
Anti-Idiotypic Antibodies
9%
Skeletal Muscle
9%
Biopsy
9%
Reading Frames
8%
Sarcopenia
8%
Muscular Dystrophy, Limb-Girdle, Type 1D
8%
Antibodies
7%
Carrier State
7%
Autosomal dominant Inclusion body myopathy
7%
Genetic Testing
6%
Exanthema
6%