Medicine and Dentistry
Glycogen Storage Disease
100%
Empagliflozin
100%
Neutropenia
79%
Neutrophil
58%
Disorders of Mitochondrial Functions
50%
Newborn Screening
50%
Quality of Life
29%
Symptom
26%
Hypertrophic Cardiomyopathy
25%
Mitochondrial DNA
25%
Kidney Tubule Disorder
25%
Bone Fragility
25%
Patient-Reported Outcome
25%
Isomerase
25%
Spinal Muscular Atrophy
25%
Osteoblast
25%
Fracture
25%
Hyperammonemia
25%
Adipocyte
25%
Cyanocobalamin
25%
Hypotonia
20%
Granulocyte Colony Stimulating Factor
18%
Renal Tubular Acidosis
16%
Exome Sequencing
16%
Sodium Glucose Cotransporter 2 Inhibitor
16%
Diseases
14%
Succinylacetone
13%
Type I Tyrosinemia
13%
Health Care Cost
12%
Osteoplasty
12%
Femur Fracture
12%
Mineralization
12%
Cerebral Atrophy
12%
Fat Droplet
12%
down Regulation
12%
Bone Defect
12%
Osteoblastogenesis
12%
Bone Development
12%
Disease
12%
Obesity
12%
Bone Mass
12%
Cancellous Bone
12%
Real-Time Polymerase Chain Reaction
12%
Skin Fibroblast
12%
Respiratory Failure
12%
Mesenchymal Stem Cell
12%
Absence
12%
Proteomics
12%
RNA Sequence
12%
Disease Course
11%
Biochemistry, Genetics and Molecular Biology
Exome Sequencing
40%
Genetics
25%
Neurexin
25%
Isoform
25%
Plexin
25%
Amelogenesis
25%
Leigh's Disease
25%
Leber's Hereditary Optic Neuropathy
25%
HK1
25%
Isomerase
25%
GABAergic Transmission
25%
Fluoxetine
25%
Newborn Period
25%
Loxapine
25%
MELAS Syndrome
25%
Hemodialysis
25%
Electrophysiology
25%
Whole Cell
25%
Riluzole
25%
Heteroplasmy
25%
Inorganic Pyrophosphatase
25%
Mental Retardation
25%
1,5-Anhydroglucitol
25%
Dihydroorotase
18%
Intracellular Signaling
12%
Cell Surface Protein
12%
Penetrance
12%
Promoter Region
12%
Bone Mass
12%
Glucose Blood Level
10%
Genome Sequencing
9%
Semaphorin
8%
Genetic Evaluation
6%
Exome
6%
Aminoacyl tRNA Synthetase
6%
MPV17
6%
DGUOK
6%
Brain Development
6%
Synaptic Transmission
6%
Infancy
6%
Observational Study
6%
Psychomotor Development
6%
Cell pH
6%
Cognitive Development
6%
Codon
6%
Polyacrylamide Gel Electrophoresis
6%
Mitochondrial Disease
6%
Steady State
6%
Mitochondrial DNA
5%
Proband
5%
Neuroscience
Leigh's Disease
25%
Optic Neuropathy
25%
Glucose Transporter 1
25%
GABAergic Transmission
25%
Synthetase
25%
Mitochondrial Disease
25%
In Vitro
25%
Phenylalanine
25%
Status Epilepticus
25%
Encephalopathy
12%
Exome Sequencing
11%
Corpus Callosum
8%
Cell Membrane
8%
Choroid Plexus
8%
Amino Acid Transfer RNA Ligase
8%
Ketogenic Diet
7%
Fluoxetine
6%
Riluzole
6%
Quinidine
6%
Loxapine
6%
Artificial Neural Network
6%
Electrophysiology
6%
Amino Acid
6%
Focal Epilepsy
5%
Mitochondrial DNA
5%
ICD-10
5%
Whole Genome Sequencing
5%
