Keyphrases
Limb-girdle muscular Dystrophy
100%
Muscular Dystrophy
87%
Duchenne muscular Dystrophy
75%
Pediatric
65%
Electromyography
61%
Skeletal muscle
56%
Spinal muscular Atrophy
53%
Myasthenia Gravis
49%
MEGF10
48%
Myopathy
43%
Nerve Conduction Studies
41%
Neuromuscular Disease
41%
Pathogenic Variants
36%
Myopathic
35%
Electrophysiologic
34%
Muscle Disease
31%
Cockayne Syndrome
29%
Congenital Myopathy
29%
Muscle Biopsy
28%
Chronic Inflammatory Demyelinating Polyradiculoneuropathy
28%
Child Neurology
28%
Electrodiagnosis
28%
Clinical Trials
28%
Seizure
27%
JAG2
24%
Diagnostic Approach
24%
Motor Neuron Disease
24%
Spinal muscular Atrophy Type III
23%
Novel mutation
23%
Motor Function
23%
Adenovirus
22%
Glycogen Storage Disease Type IV
21%
United States
20%
Genetic Testing
20%
Dystrophin
20%
Myoblast
20%
Motor Neuron
20%
Intravenous Immunoglobulin (IVIg)
20%
Neuropathy
19%
Pompe Disease
19%
Human Skeletal muscle
19%
Exome Sequencing
19%
Developmental Delay
18%
Clinical Features
18%
Autosomal Recessive
18%
Becker muscular Dystrophy
17%
Muscle Type
17%
Barth Syndrome
17%
Pediatric Neurologist
17%
Axonal Loss
17%
Medicine and Dentistry
Pediatrics
82%
Diseases
71%
Electromyography
52%
Disease
42%
Clinical Trial
41%
Neuropathy
38%
Muscular Dystrophy
33%
Nerve Conduction Study
31%
Skeletal Muscle
29%
Spinal Muscular Atrophy
28%
Neuromuscular Disorder
28%
Pediatric Neurology
28%
Myasthenia gravis
28%
Polyradiculoneuropathy
28%
Polyneuropathy
27%
Electrodiagnosis
24%
Kugelberg Welander Disease
23%
Spinal Muscular Atrophy Type 2
23%
Limb Girdle Muscular Dystrophy
22%
Cockayne Syndrome
22%
Adeno-Associated Virus
22%
Motor Performance
22%
Observational Study
21%
Weakness
20%
Myopathy
20%
Magnetic Resonance Imaging
19%
Duchenne Muscular Dystrophy
19%
Dystrophin
17%
Immunoglobulin
17%
Health Care Cost
17%
Epileptic Seizure
17%
Muscle Disease
15%
Myotonic Dystrophy
15%
Axon
15%
Afferent Nerve Fiber
14%
Peroneal Neuropathy
14%
Extraocular Muscle
14%
Fibrosis
14%
Glycogen Storage Disease Type IV
14%
Heterogeneous Nuclear Ribonucleoprotein L
14%
Targeted Therapy
14%
Clinical Feature
14%
Genetic Screening
14%
Action Potential
13%
Neuromuscular Disease
12%
Gene Therapy
12%
Patient Referral
11%
Muscle Biopsy
11%
Kallmann Syndrome
10%
Tubulin
10%
Biochemistry, Genetics and Molecular Biology
Skeletal Muscle
98%
Genetics
98%
Exome Sequencing
33%
Allele
32%
Myogenesis
30%
MicroRNA
28%
Genetic Screening
28%
Dystrophin
24%
Fibroblast
23%
Adeno Associated Virus
22%
Zebra Fish
22%
Creatine Kinase Blood Level
22%
Missense Mutation
21%
JAG2
21%
Linkage Analysis
18%
Electrodiagnosis
17%
Genotype Phenotype Correlation
17%
Genomics
17%
Missense
16%
Motor Performance
15%
Autosomal Recessive Inheritance
15%
Amino Acids
15%
Clinical Trial
15%
Sarcoglycan
15%
Cell Proliferation
14%
TUBB3
14%
Glycosylation
14%
Subcellular Localization
14%
Gene Linkage
14%
Proband
14%
Next Generation Sequencing
13%
Cell Migration
13%
Autosomal Dominant Inheritance
12%
Enzyme Activity
12%
Dystroglycan
12%
Mitochondrial DNA
12%
Protein Kinase B
12%
C2C12
12%
Gene Expression
10%
Growth Factor-Like Domain
10%
Dynamin
10%
Epidermal Growth Factor
10%
Exon
10%
Splice Site Mutation
10%
Cysteine
10%
Mitochondrial Disorder
10%
RNA Sequence
10%
Magnetic Resonance Imaging
10%
Muscle Regeneration
9%
CAPN3
9%
