Medicine and Dentistry
Patient
77%
Myopathy
51%
Disease
32%
Diagnosis
29%
Syndrome
28%
Gene
27%
Rhabdomyolysis
26%
Centronuclear Myopathy
21%
Child
20%
Family
19%
Therapeutic Procedure
17%
Magnetic Resonance Imaging
16%
Muscle Biopsy
15%
Neuromuscular Disease
15%
Symptom
14%
Clinical Feature
14%
Malignant Hyperthermia
13%
Multiminicore Disease
13%
Central Core Disease
11%
Myalgia
10%
Cataract
10%
Weakness
8%
Differential Diagnosis
8%
Girl
8%
Duchenne Muscular Dystrophy
8%
Genetic Disorder
8%
Therapeutics
7%
Protein
7%
Exercise
7%
Male
7%
DeJerine-Sottas Disease
6%
Myasthenia gravis
6%
Hypotonia
6%
Infant
6%
Ryanodine Receptor 1
6%
Anesthetic
5%
Muscle Disease
5%
Corpus Callosum Agenesis
5%
Hypopigmentation
5%
Follow up
5%
Anesthesia
5%
Congenital Myasthenic Syndrome
5%
Respiratory Failure
5%
Metabolism
5%
Dynamin II
5%
Scoliosis
5%
Nemaline Myopathy
5%
Exercise Intolerance
5%
Biochemistry, Genetics and Molecular Biology
Gene
87%
Genetics
43%
Spectrum
38%
Protein
29%
Skeletal Muscle
16%
Magnetism
11%
Exon
9%
Clinical Trial
9%
BIN1
7%
DNM2
6%
MYH7
6%
Ultrasound
5%
Next Generation Sequencing
5%
Missense
5%
Genotype
5%
Neuroscience
Muscle Disorder
100%
Neuromuscular Disorder
15%
Neuromuscular
13%
Magnetic Resonance Imaging
12%
Magnetic Resonance Imaging
11%
RYR1
9%
Differential Diagnosis
7%
Hypotonia
7%