Medicine and Dentistry
Myopathy
71%
Diseases
43%
Serum
32%
Myasthenia gravis
28%
Phenotype
24%
Muscle Weakness
19%
Lesion
18%
Clinical Feature
16%
Antibody
15%
Onset Age
14%
Dysferlinopathy
14%
Muscle Biopsy
14%
Exon
14%
Magnetic Resonance Imaging
13%
Limb Girdle Muscular Dystrophy
12%
Prognosis
12%
Neuron Specific Enolase
12%
Creatine Kinase
11%
Neuromuscular Disease
11%
Peripheral Neuropathy
11%
Distal Myopathy
11%
Duchenne Muscular Dystrophy
10%
Periodic Paralysis
10%
Muscular Dystrophy
10%
Muscle Disease
10%
Gene Mutation
9%
Autosomal Recessive Inheritance
9%
Dysferlin
9%
White Matter
9%
Dermatomyositis
8%
Follow up
8%
Facioscapulohumeral Muscular Dystrophy
8%
Dystonia
8%
Transthyretin
8%
Glycogen Storage Disease Type II
8%
B-Cell Activating Factor
8%
Thymectomy
8%
Focal Dystonia
8%
Dystrophinopathy
8%
Sequela
8%
Neuropathy
8%
Pathogenesis
8%
Multiplex Ligation Dependent Probe Amplification
7%
Thomsen Disease
7%
Phosphotransferase
7%
Protein
7%
Seizure
7%
Prevalence
7%
Miyoshi Myopathy
7%
Nystagmus
7%
Agricultural and Biological Sciences
Mutation
100%
Phenotype
37%
Antibodies
21%
Muscle Fiber
16%
Creatine Kinase
16%
Laboratories
14%
Proteins
14%
Magnetic Resonance Imaging
11%
Prevalence
10%
Genotype
9%
Amyloid
9%
Dysferlin
9%
Inclusion Bodies
8%
Insulin Resistance
8%
Gender Differences
8%
Spinal Cord
8%
Immunohistochemistry
7%
Motor Neuron
6%
Palate
6%
Observational Studies
6%
Vacuole
6%
Shotgun Sequencing
6%
Exome Sequencing
5%
Action Potential
5%
Allele
5%
Polymorphism
5%
Risk Factors
5%
CAPN3
5%
Histology
5%
Headache
5%
Dystrophin
5%
Neuroscience
Muscular Dystrophy
39%
Myasthenia gravis
32%
Phenotype
25%
Creatine Kinase
16%
Peripheral Neuropathy
14%
Antibodies
14%
Neuromuscular
14%
Amyotrophic Lateral Sclerosis
12%
Neuron Specific Enolase
12%
White Matter
12%
Skeletal Muscle
12%
Magnetic Resonance Imaging
11%
Kinase
10%
Proteome
9%
Gene Mutation
9%
Hyperkalemic Periodic Paralysis
9%
Exon
8%
Dystonia
8%
Multiplex Ligation-Dependent Probe Amplification
7%
Nystagmus
7%
Myotonia congenita
6%
Palate
6%
Hyporeflexia
6%
Motor Neuron
6%
Immunohistochemistry
5%
CLCN1
5%
Exome Sequencing
5%
Amyloid
5%
Alzheimer's Disease
5%
Dysferlin
5%
Action Potential
5%
Histology
5%
Carbon Monoxide
5%
Nerve Conduction Study
5%
Somatosensory Evoked Potential
5%
Spinal Muscular Atrophy
5%
Hypotonia
5%
Nerve Conduction
5%