Biochemistry, Genetics and Molecular Biology
Fibroblast
75%
Mitochondrial DNA
66%
Newborn Screening
66%
Exome Sequencing
60%
Mitochondrial Disorder
44%
Mitochondrial Disease
41%
Genetics
37%
Isomerase
33%
Hemodialysis
33%
Heteroplasmy
33%
Inorganic Pyrophosphatase
33%
CUL3
33%
Pyrophosphatase
33%
Galactose
33%
Leber Hereditary Optic Neuropathy
33%
Synthase
33%
Metabolic Pathway
33%
Neurexin
33%
Gamma-Aminobutyric Acid
33%
Adipocyte
33%
Quinidine
33%
Artificial Neural Network
33%
Osteoblast
33%
Adenosine Triphosphate
33%
RNA Processing
33%
Peptidase
33%
Calcium Signaling
33%
Uridine
25%
Enzyme
20%
Bone Mass
16%
Mineralization
16%
Bone Development
16%
Electron Transport Chain
16%
Stromal Cell
16%
Swallow (Bird)
16%
Bone Remodeling
16%
RUNX2
16%
SMAD
16%
RNA Sequence
16%
Transfer RNA
16%
RNA
16%
Glutamic Acid
16%
Proteomics
16%
Real-Time Polymerase Chain Reaction
16%
down Regulation
16%
Lipid Droplet
16%
Mitochondrial Genome
16%
Metabolic Disorder
15%
Newborn Period
12%
Uniporter
12%
Medicine and Dentistry
Glycogen Storage Disease
100%
Empagliflozin
100%
Neutrophil
77%
Neutropenia
72%
Disorders of Mitochondrial Functions
72%
Newborn Screening
66%
Synthetase
66%
Phenylalanine
36%
Hypertrophic Cardiomyopathy
33%
Mitochondrial DNA
33%
Kidney Tubule Disorder
33%
Isomerase
33%
Hyperammonemia
33%
Cyanocobalamin
33%
Hemodialysis
33%
Supplementation
33%
Adenosine Triphosphate
33%
Modified Atkins Diet
33%
Glycogen Storage Disease Type I
33%
Diseases
26%
Health Care Cost
23%
Renal Tubular Acidosis
22%
Disease Course
21%
Succinylacetone
18%
Type I Tyrosinemia
18%
Bone Remodeling
16%
Granulocyte Colony Stimulating Factor
16%
Neonatal Infant
14%
Psychomotor Development
14%
Genetic Screening
13%
Amino Acid
13%
Differential Diagnosis
12%
Quality of Life
12%
Hypotonia
11%
Health Care
11%
Creatine Kinase
11%
Dilated Cardiomyopathy
11%
Lactic Acidosis
11%
MELAS Syndrome
11%
Newborn Period
11%
Infancy
11%
Rare Disease
11%
Physical Disease by Body Function
9%
Diagnosis
8%
Emotion
8%
Supportive Care
8%
Social Support
8%
Personal Experience
8%
Social Participation
8%
Awareness
8%
Pharmacology, Toxicology and Pharmaceutical Science
Glycogen Storage Disease
66%
Empagliflozin
66%
Neutropenia
38%
Mitochondrial DNA
33%
Hypertrophic Cardiomyopathy
33%
Disorders of Mitochondrial Functions
33%
Kidney Tubule Disorder
33%
Repurposing
33%
Vaccine
33%
Kidney Tubule Acidosis
22%
Granulocyte Colony Stimulating Factor
11%
Disease
11%
Creatine Kinase
11%
MELAS Syndrome
11%
Lactic Acidosis
11%
Congestive Cardiomyopathy
11%
Syndrome
11%
Muscle Hypotonia
11%
Disease Course
11%
Rare Disease
11%
Physical Disease by Body Function
9%
Muscle Fatigue
8%
Rhabdomyolysis
8%
Muscle Weakness
8%
Microalbuminuria
6%
International Classification of Diseases
5%
ICD-10
5%
Pharmacoeconomics
5%
