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