Medicine and Dentistry
DeJerine-Sottas Disease
100%
Neuropathy
28%
Magnetic Resonance Imaging
26%
Echography
25%
Kawasaki Disease
20%
Sex Difference
20%
Linkage Analysis
14%
Pleura Effusion
14%
Coughing
13%
Fatty Liver
13%
Visual Stimulation
13%
Optic Nerve Atrophy
13%
Deep Vein Thrombosis
13%
Total Knee Arthroplasty
13%
Pulmonary Embolism
13%
Cataract
13%
Intima-Media Thickness
13%
Laminectomy
13%
Spondylolysis
13%
Spondylolisthesis
13%
Multidetector Computed Tomography
13%
K-Complex
13%
MYH7
13%
Distal Myopathy
13%
Mitofusin 2
13%
Neonate
13%
Electromyography
13%
Diffusion Tensor Imaging
13%
Thoracic Vertebra
13%
Trachea
13%
Choroid Plexus
13%
Angioleiomyoma
13%
Tissue Structure
13%
Heat Shock Protein 22
13%
Small Heat Shock Protein
13%
Disease
12%
Neck
12%
Sural Nerve
10%
Autosomal Recessive Inheritance
9%
Exome Sequencing
9%
Diagnosis
8%
Clinical Feature
7%
Patient with Kawasaki Disease
6%
Mycoplasma Pneumonia
6%
Alanine Aminotransferase
6%
Aspartate Aminotransferase
6%
Body Surface
6%
Necrosis
6%
Cooperation
6%
Tuberculous Lymphadenitis
6%
Neuroscience
Charcot-Marie-Tooth Disease
73%
Neuropathy
73%
Exome Sequencing
38%
Temporal Lobe Epilepsy
26%
Functional Magnetic Resonance Imaging
23%
Gray Matter
21%
Diffusion Tensor Imaging
20%
Cognitive Disorders
19%
Memory Disorder
15%
Missense Mutation
14%
Myoblast
13%
Adductor Magnus Muscle
13%
Brain Activation
13%
Heat Shock Protein 22
13%
Small Heat Shock Protein
13%
Mitofusin 2
13%
Functional Connectivity
13%
Amino Terminal Sequence
13%
Sural Nerve
10%
Peripheral Myelin Protein 22
10%
Magnetic Resonance Imaging
9%
Brain Lesion
8%
In Vitro
8%
In Vivo
6%
Creatine Kinase
6%
Enzyme Activity
6%
Parahippocampal Gyrus
6%
Necrosis
6%
Spinocerebellar Ataxia
6%
Chromosome 10
6%
Open Reading Frame
6%
Polyneuropathy
6%
Voxel-Based Morphometry
6%
Temporal Lobe
6%
Ataxia
5%
Brain Network
5%
Executive Function
5%
Wechsler Intelligence Scale for Children
5%
Magnetic Resonance Imaging
5%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Inheritance
27%
Exome Sequencing
25%
Wild Type
15%
Autosomal Dominant Inheritance
14%
Linkage Analysis
13%
Transgenic Mouse
13%
Optic Atrophy 1
13%
Synapsin I
13%
HADHB
13%
Ganglioside
13%
Adolescence
13%
Missense Mutation
13%
Heat Shock Protein
13%
Fibrinogen
13%
Peripheral Myelin Protein 22
8%
Myelin
7%
Gene Mutation
7%
Zebra Fish
6%
Gene Linkage Disequilibrium
6%
Candidate Gene
6%
Single Nucleotide Polymorphism
6%
Integral Membrane Protein
6%
Gene Linkage
6%
Crystallin
6%
Codon
6%
Nerve Conduction
5%
