Medicine and Dentistry
DeJerine-Sottas Disease
100%
Peripheral Nervous System
70%
Spinal Muscular Atrophy
58%
Genetic Disorder
58%
Polyneuropathy
52%
Molecular Diagnosis
47%
Neurofilament
47%
Light Chain
47%
Disease Exacerbation
47%
Biological Marker
47%
Alanine Transfer RNA Ligase
47%
Prevalence
47%
Gene Mutation
47%
Myokymia
47%
Awareness
47%
Disease Severity
34%
Exon
27%
Achilles Reflex
23%
Pes cavus
23%
Thomsen Disease
23%
Foot Malformation
23%
Early Diagnosis
15%
Kennedy Disease
11%
Dystrophinopathy
11%
Limb Girdle Muscular Dystrophy
11%
Facioscapulohumeral Muscular Dystrophy
11%
Genetic Analysis
11%
Myotonic Dystrophy
11%
CLCN1
11%
Retrospective Study
11%
Next Generation Sequencing
11%
Gene Frequency
11%
DNA Isolation
7%
Real-Time Polymerase Chain Reaction
7%
Multiplex Ligation Dependent Probe Amplification
7%
Organ Systems
5%
Clinical Feature
5%
Segregation Analysis
5%
Lower Limb
5%
Weakness
5%
Biochemistry, Genetics and Molecular Biology
Blood Plasma
94%
Exon
58%
SMN1
58%
Prevalence
47%
Transfer RNA
47%
Light Chain
47%
Neurofilament Light
47%
Genotyping
47%
Visual Evoked Potential
47%
Metabolite
41%
Real-Time Polymerase Chain Reaction
23%
Multiplex Ligation-Dependent Probe Amplification
23%
Locked Nucleic Acid
23%
DNA Isolation
23%
CAPN3
11%
Next Generation Sequencing
11%
CLCN1
11%
Retrospective Study
11%
SPG11
11%
Gene Frequency
11%
Valine
11%
Blood Level
5%
Liquid Chromatography-Mass Spectrometry
5%
Genetic Screening
5%
Small Molecule
5%
Metabolome Analysis
5%
Pharmacology, Toxicology and Pharmaceutical Science
Anakinra
94%
Syndrome
94%
Spinal Muscular Atrophy
58%
Prevalence
47%
Thomsen Disease
23%
Genetic Disorder
11%
Kennedy Disease
11%
Facioscapulohumeral Muscular Dystrophy
11%
Myotonic Dystrophy
11%
Limb Girdle Muscular Dystrophy
11%
Dystrophinopathy
11%
Retrospective Study
11%
Clonic Seizure
9%
Disease Course
9%
Locked Nucleic Acid
7%
Intractable Epilepsy
5%
Epileptic State
5%
