Medicine & Life Sciences
Myofibrillar Myopathy
100%
Congenital Myasthenic Syndromes
85%
Mutation
60%
Muscle Weakness
39%
Muscles
38%
Cholinergic Receptors
35%
Muscular Dystrophies
34%
Crystallins
24%
Muscular Diseases
23%
Desmin
21%
Distal Myopathies
21%
Phenotype
19%
Myositis
17%
Congenital Structural Myopathies
15%
Dermatomyositis
15%
Cardiomyopathies
14%
Biopsy
14%
Proteins
14%
Nemaline Myopathies
13%
peripheral membrane protein 43K
13%
Natural History
13%
Extremities
13%
Myasthenia Gravis
13%
Whole Exome Sequencing
13%
Genes
12%
Electron Microscopy
10%
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
9%
Genetic Testing
9%
Filamins
9%
dolichyl-phosphate alpha-N-acetylglucosaminyltransferase
9%
Agrin
8%
Exome
8%
Therapeutics
8%
Myotonia Congenita
8%
Hypotonia-Cystinuria Syndrome
8%
Endplate Acetylcholinesterase Deficiency
8%
Neurology
8%
Actin-Accumulation Myopathy
8%
Mitochondrial Complex III Deficiency
8%
Vesicle-Associated Membrane Protein 1
7%
Limb-Girdle Muscular Dystrophies
7%
Pediatrics
7%
Myopathy, Myofibrillar, Desmin-Related
7%
Plectin
7%
nusinersen
7%
Limb-girdle muscular dystrophy autosomal recessive
7%
Glucocorticoids
7%
Multiple pterygium syndrome
7%
Giant Axonal Neuropathy
7%