Medicine and Dentistry
Patient
100%
Age
62%
Spinal Muscular Atrophy
38%
Infant
37%
Duchenne Muscular Dystrophy
36%
Assessment
30%
Child
26%
Upper Limb
25%
Nusinersen
21%
Muscle
20%
Therapeutic Procedure
19%
Diseases
16%
Vision
13%
Spinal Muscular Atrophy Type 2
12%
Prematurity
12%
Kugelberg Welander Disease
11%
Inpatient
11%
Magnetic Resonance Imaging
11%
Deterioration
11%
Follow up
11%
Gene
10%
Motor Performance
9%
Development
9%
Werdnig Hoffmann Disease
9%
Phenotype
9%
Exon
8%
Myopathy
8%
Neuromuscular Disease
8%
Diagnosis
8%
Brain
8%
Combination Therapy
7%
Muscular Dystrophy
7%
Severe Myoclonic Epilepsy of Infancy
7%
Aptitude
7%
Adult
7%
Analysis
6%
Lesion
6%
Neurologic Examination
6%
Attention
6%
Sleep Disorder
6%
Six Minute Walk Test
5%
Clinical Trial
5%
Comprehension
5%
Experience
5%
Psychology
Children
31%
Duchenne Muscular Dystrophy
25%
Infant
21%
Groups
16%
Assessment
15%
Spinal Muscular Atrophy
12%
Treatment
11%
Abilities
11%
Cerebral Palsy
7%
Tools
6%
Attention
6%
Preschool
5%
Sleep
5%
Biochemistry, Genetics and Molecular Biology
Nested Gene
21%
Mutation
18%
Age
17%
Genetics
12%
Phenotype
11%
SMN2
7%
Development
6%
Spectrum
5%
Time
5%
