Medicine & Life Sciences
Muscular Diseases
100%
Congenital Myasthenic Syndromes
87%
Mutation
82%
Cholinergic Receptors
68%
Muscles
55%
Distal Myopathies
36%
Muscle Weakness
35%
Inclusion Body Myositis
28%
Genes
25%
Muscular Dystrophies
24%
Myotonic Dystrophy
22%
Mitochondrial Diseases
22%
Biopsy
21%
Phenotype
20%
Myotonia Congenita
18%
Mitochondrial DNA
18%
Myasthenia Gravis
17%
peripheral membrane protein 43K
16%
Rhabdomyolysis
15%
Kinetics
15%
Anoctamins
14%
Valosin Containing Protein
13%
Nemaline Myopathies
13%
Creatine Kinase
13%
Vacuolar myopathy
13%
Missense Mutation
13%
Vacuoles
12%
Atrophy
12%
Myalgia
12%
Amyloid
12%
1 Rippling muscle disease
12%
Congenital Structural Myopathies
12%
Chronic Progressive External Ophthalmoplegia
11%
Amyloidosis
11%
Minicore Myopathy with External Ophthalmoplegia
11%
Electromyography
10%
Facioscapulohumeral Muscular Dystrophy
10%
Tremor
10%
Acetylcholine
9%
Camptocormia
9%
Extremities
9%
Myotonia
9%
High-Throughput Nucleotide Sequencing
9%
Limb-Girdle Muscular Dystrophies
9%
Optic Atrophy
9%
Mitochondrial Myopathies
9%
Fathers
9%
Skeletal Muscle
8%
Nonaka type Distal myopathy
8%
Psychologic Desensitization
8%