Keyphrases
Mitochondrial Dysfunction
100%
Mitochondria
90%
SCN1A
57%
Cerebral Venous Sinus Thrombosis
57%
Metabolic Syndrome
40%
Type 2 Diabetes Mellitus (T2DM)
38%
Heart Failure
38%
Compound Heterozygous mutation
34%
Non-alcoholic Fatty Liver Disease (NAFLD)
31%
Biallelic
31%
Clinical Spectrum
31%
Genotype
31%
Viral Infection
28%
15q13.3
28%
MSI2
28%
Alcoholic Liver Disease
28%
Hypotonia
28%
EEF2
28%
Disease-related
28%
Neurodevelopmental Disorders
28%
Encephalopathy
28%
Metabolic Acidosis
28%
Gain-of-function mutation
28%
Musashi-2
28%
COVID-19
28%
Kcnj16
28%
Global Developmental Delay
28%
Acute Encephalopathy
28%
Facial Dysmorphism
28%
Impaired Vision
28%
Promoter Variants
28%
Microdeletion
28%
Cardiac Hypertrophy
28%
MPV17
28%
Mitochondrial DNA Maintenance
28%
Hypokalemic
28%
Multiple acyl-CoA Dehydrogenase Deficiency
28%
Smyd1
28%
Extremely Preterm Infants
28%
L-2-hydroxyglutaric Aciduria
28%
Mitochondrial Citrate Carrier
28%
Molecular Aspects
28%
Germ Cells
28%
Biochemical Features
28%
Neurological Development
28%
RNA Interference
28%
Epileptic Encephalopathy
28%
Intraventricular Hemorrhage
28%
SLC25A4
28%
Ornithine Transcarbamylase Deficiency
28%
Biochemistry, Genetics and Molecular Biology
Mitochondrial Disorder
90%
Mitochondrion
84%
Mitochondrial DNA
61%
Genotyping
60%
Methylenetetrahydrofolate Reductase
57%
Homocysteine
57%
Mitochondrial Genome
47%
Messenger RNA
47%
Missense
38%
Mitochondrial Disease
38%
Exome Sequencing
32%
EEF2
28%
Isoform
28%
RNA-induced Silencing Complex
28%
Metabolic Disorder
28%
CHRNA7
28%
Basolateral Membrane
28%
ETFA
28%
Protein Subunit
28%
Oxidoreductase
28%
Dehydrogenase
28%
MPV17
28%
Acyl-CoA
28%
Promoter Region
28%
Germline
28%
Germ Cell
28%
Vascular Endothelial Growth Factor
28%
RNAI
28%
Genome Sequencing
19%
TRPM1
19%
Membrane Potential
19%
Genetics
17%
Dyslipidemia
14%
Aminoacyl tRNA Synthetase
14%
Protein Complexes
14%
Oxidative Phosphorylation
14%
Potassium Channel
14%
Triglyceride
14%
Oxidative Stress
14%
KCNJ10
14%
Insulin Resistance
14%
Cardiac Muscle Cell
14%
ATPase
14%
Adenosine Triphosphate
14%
Cell Energy
14%
HDL-Cholesterol
14%
Alpha Chain
14%
Transfer RNA
14%
Kir5.1 Channel
14%
Voltage-Gated Channel
14%
Medicine and Dentistry
Mitochondrial Disorder
61%
Brain Disease
57%
Cerebral Venous Sinus Thrombosis
57%
Cerebral Sinus Thrombosis
57%
Maturity Onset Diabetes of the Young
42%
Mitochondrion
42%
Metabolic Syndrome
40%
Methylenetetrahydrofolate Reductase
32%
Homocysteine
32%
Nonalcoholic Fatty Liver
31%
Virus Infection
28%
Aciduria
28%
Alcohol-Related Liver Disease
28%
Metabolic Acidosis
28%
Vasculotropin
28%
Acute Brain Disease
28%
Cerebral Blindness
28%
Ornithine Transcarbamylase Deficiency
28%
Promoter Region
28%
COVID-19
28%
Glutaric Acidemia Type 2
28%
Cerebral Hemorrhage
28%
Prematurity
28%
Oxidative Stress
27%
Infection
23%
Steatosis
21%
Fatty Liver
21%
Disease
20%
Clinical Feature
19%
Basolateral Membrane
19%
Exome Sequencing
17%
Neonatal Infant
14%
Genetic Susceptibility
14%
Disease Predisposition
14%
Identified Patient
14%
Respiratory Failure
14%
Water-Electrolyte Imbalance
14%
Respiratory Tract Infection
14%
Diagnosis
14%
Chronic Liver Disease
14%
Virus Etiology
14%
Lactic Acidosis
14%
Genetic Background
14%
Central Nervous System
14%
Influenza
14%
Hyperammonemia
11%
Magnetic Resonance Imaging
11%
Apoplexy
11%
Pregnancy
10%
Public Health
10%
