Medicine and Dentistry
Patient
100%
Amyotrophic Lateral Sclerosis
58%
Neuropathy
28%
Gene
21%
Diseases
20%
Inpatient
19%
Diagnosis
17%
Phenotype
13%
Nerve Biopsy
12%
Polyneuropathy
11%
Transthyretin
9%
DeJerine-Sottas Disease
9%
Therapeutic Procedure
8%
Edoxaban
8%
Immunoglobulin M
7%
Combination Therapy
7%
Sural Nerve
7%
ATTR Amyloidosis
7%
Frontotemporal Lobar Degeneration
7%
Survival
6%
Induced Pluripotent Stem Cell
6%
Magnetic Resonance Imaging
6%
Follow up
5%
Polyradiculoneuropathy
5%
Peripheral Neuropathy
5%
Evaluation Study
5%
Association
5%
Atrial Fibrillation
5%
Neuroscience
Amyotrophic Lateral Sclerosis
88%
Gene
40%
Peripheral Neuropathy
30%
Phenotype
26%
Frontotemporal Dementia
11%
SOD1
10%
Polyneuropathy
9%
Immunoglobulin M
8%
Upper Motor Neuron
7%
Muscle Disorder
7%
Charcot-Marie-Tooth Disease
6%
Lower Motor Neuron
6%
Amyloidosis
6%
Intravenous Immunoglobulin
5%
Transthyretin
5%
Exon
5%
Fibroblast
5%
Edoxaban
5%
Botulinum Toxin
5%
Biochemistry, Genetics and Molecular Biology
Mutation
49%
Nested Gene
32%
Phenotype
15%
SOD1
11%
Survival
8%
FUS
8%
Genetics
7%
Age
6%
Fibroblast
6%
Upper Motor Neuron
6%
TARDBP
5%
