Medicine & Life Sciences
1 Rippling muscle disease
8%
Acetylcholine
7%
Amyloid
8%
Amyloidosis
8%
Anoctamins
10%
Atrophy
9%
Biopsy
18%
Camptocormia
7%
Cholinergic Receptors
50%
Chronic Progressive External Ophthalmoplegia
8%
Congenital Myasthenic Syndromes
65%
Congenital Structural Myopathies
8%
Creatine Kinase
12%
Distal Myopathies
26%
Electromyography
9%
Extremities
7%
Facioscapulohumeral Muscular Dystrophy
8%
Genes
19%
Genetic Testing
6%
High-Throughput Nucleotide Sequencing
8%
Immunoglobulin G
7%
Inclusion Body Myositis
21%
Kinetics
11%
Limb-Girdle Muscular Dystrophies
8%
Minicore Myopathy with External Ophthalmoplegia
8%
Missense Mutation
9%
Mitochondrial Diseases
16%
Mitochondrial DNA
13%
Mitochondrial Myopathies
7%
Muscle Weakness
27%
Muscles
45%
Muscular Diseases
100%
Muscular Dystrophies
19%
Mutation
63%
Myalgia
9%
Myasthenia Gravis
13%
Myotonia
10%
Myotonia Congenita
14%
Myotonic Dystrophy
18%
Nemaline Myopathies
16%
Nonaka type Distal myopathy
6%
Optic Atrophy
6%
peripheral membrane protein 43K
11%
Phenotype
16%
Rhabdomyolysis
14%
Skeletal Muscle
6%
Tremor
7%
Vacuolar myopathy
11%
Vacuoles
9%
Valosin Containing Protein
17%