Medicine & Life Sciences
Muscular Diseases
100%
Congenital Myasthenic Syndromes
65%
Mutation
64%
Cholinergic Receptors
51%
Muscles
45%
Muscle Weakness
27%
Distal Myopathies
27%
Inclusion Body Myositis
21%
Genes
20%
Muscular Dystrophies
19%
Myotonic Dystrophy
18%
Biopsy
18%
Valosin Containing Protein
17%
Nemaline Myopathies
16%
Phenotype
16%
Mitochondrial Diseases
16%
Myotonia Congenita
14%
Mitochondrial DNA
13%
Myasthenia Gravis
13%
Rhabdomyolysis
12%
Creatine Kinase
12%
peripheral membrane protein 43K
12%
Kinetics
12%
Vacuolar myopathy
11%
Anoctamins
11%
Myotonia
10%
Missense Mutation
9%
Vacuoles
9%
Atrophy
9%
Myalgia
9%
Amyloid
9%
1 Rippling muscle disease
9%
Congenital Structural Myopathies
8%
Chronic Progressive External Ophthalmoplegia
8%
Facioscapulohumeral Muscular Dystrophy
8%
Amyloidosis
8%
Electromyography
8%
Minicore Myopathy with External Ophthalmoplegia
8%
Limb-Girdle Muscular Dystrophies
8%
Mitochondrial Myopathies
7%
Extremities
7%
Immunoglobulin G
7%
Tremor
7%
Acetylcholine
7%
Camptocormia
7%
High-Throughput Nucleotide Sequencing
7%
Skeletal Muscle
7%
Optic Atrophy
6%
Nonaka type Distal myopathy
6%
Fathers
6%