Medicine and Dentistry
Patient
75%
DeJerine-Sottas Disease
54%
Gene
45%
Family
32%
Muscle
27%
Peripheral Neuropathy
20%
Brain
20%
Inpatient
19%
Phenotype
19%
Tooth
18%
Disease
18%
Analysis
17%
Child
16%
Autosomal Dominant Inheritance
14%
Myopathy
13%
Lesion
13%
Sex Difference
12%
Neuropathy
12%
Echography
12%
Kawasaki Disease
11%
Sural Nerve
11%
Experience
11%
Woman
10%
Man
10%
Cognitive Defect
10%
Epileptic Seizure
10%
Linkage Analysis
10%
Association
9%
Soft Tissue
9%
Hearing Impairment
9%
Diagnosis
9%
Pleura Effusion
9%
Evaluation Study
9%
Clinical Feature
9%
Fibrinogen
9%
Transgenic Mouse
9%
Mediastinum
9%
Functional Connectivity
9%
Memory Disorder
9%
Angioleiomyoma
9%
Language
9%
Stimulation
9%
Neonate
9%
Coughing
9%
Water
9%
Temporal Lobe Epilepsy
9%
Fatty Liver
9%
Girl
9%
Hoarseness
9%
Visual Stimulation
9%
Neuroscience
Charcot-Marie-Tooth Disease
70%
Gene
58%
Peripheral Neuropathy
30%
White Matter
21%
Brain
20%
Phenotype
20%
Seizure
19%
Temporal Lobe Epilepsy
18%
Magnetic Resonance Imaging
15%
Exome Sequencing
15%
Missense Mutation
12%
Gray Matter
12%
Cognitive Disorders
11%
Memory Disorder
9%
Hearing Loss
9%
Sural Nerve
9%
Amino Terminal Sequence
9%
Functional Connectivity
9%
Diffusion Tensor Imaging
9%
Epilepsy
9%
Synapsin I
9%
Adductor Magnus Muscle
9%
Ganglioside
9%
Small Heat Shock Protein
9%
Heat Shock Protein 22
9%
Peripheral Myelin Protein 22
6%
Brain Lesion
6%
Biochemistry, Genetics and Molecular Biology
Mutation
100%
Nested Gene
55%
Phenotype
28%
Autosomal Recessive Inheritance
20%
Autosomal Dominant Inheritance
15%
Exome Sequencing
11%
Ganglioside
9%
Transgenic Mouse
9%
HADHB
9%
Optics
9%
Linkage Analysis
9%
Hearing
9%
Heat Shock Protein
9%
Development
8%
Wild Type
8%
Spectrum
7%
Age
7%
Myelin
7%
Missense Mutation
7%
Length
6%
Mutant
6%
Gene Mutation
5%
