Keyphrases
Indonesia
82%
Iduronate 2-sulfatase Gene
56%
Photosystem II
56%
Indonesian
51%
Indonesian Patients
38%
Jakarta
25%
Novel mutation
25%
Obese Adolescents
25%
Indonesian Population
25%
Obesity
22%
Exon 9
21%
Exon
20%
Diacylglycerol Kinase
18%
Pyruvate Kinase Deficiency
18%
Mucopolysaccharidosis IVA
18%
Toddlers
18%
Modul
18%
Pada
18%
6-pyruvoyltetrahydropterin Synthase
18%
Iduronate-2-sulfatase
18%
Obese children
17%
Milk
17%
Novel Variation
15%
Amino Acids
14%
Long-chain Polyunsaturated Fatty Acids (LC-PUFA)
14%
Exon 4
13%
Exon 2
13%
Intellectual Disability
13%
Genotype
13%
Exon 8
13%
Atopic Dermatitis
13%
Randomized Controlled Trial
13%
Galactosamine
12%
Sulfatase
12%
Gene Polymorphism
12%
Indonesian children
12%
Gaucher Disease
12%
N-acetylation
12%
Exon 1
12%
Growing up
12%
Daily Consumption
12%
Exon 5
12%
Dengue Fever
12%
Healthy Individuals
12%
Silent mutation
12%
Single nucleotide Polymorphism
10%
Polymerase Chain Reaction
10%
Shock
10%
Lipid Profile
10%
Normal children
9%
Biochemistry, Genetics and Molecular Biology
Exon
100%
Mucopolysaccharidosis
70%
Iduronate-2-Sulfatase
56%
Enzyme
21%
Synthase
18%
Glycerol Kinase
18%
Glycerol Kinase Deficiency
18%
Intron
17%
Genetics
14%
Single-Nucleotide Polymorphism
13%
Galactosamine
12%
Sulfatase
12%
Gene Polymorphism
12%
Silent Mutation
12%
Amino Acids
12%
Genotyping
12%
Polyunsaturated Fatty Acid
10%
Polymerase Chain Reaction
9%
Polymerase Chain Reaction
9%
PTS (Gene)
8%
Adiponectin
8%
Glycerophospholipid
7%
Lipid Profile
7%
Sanger Sequencing
7%
Protein Characterization
7%
Intellectual Disability
7%
Prospective Study
6%
Missense Mutation
6%
Fatty Acid Desaturase
6%
Lipid Composition
6%
Dyslipidemia
6%
ALDH7A1
6%
Apolipoprotein
6%
Exercise
6%
UCP3
6%
Motor Performance
6%
Energy Expenditure
6%
Uncoupling Protein
6%
Neuronal Ceroid Lipofuscinosis
6%
Batten Disease
6%
Tripeptidyl Peptidase I
6%
Enzyme Conformation
6%
FUT2
6%
N-Acetylgalactosamine
6%
Morquio Syndrome
6%
Vitamin E
6%
Platelet Count
6%
Hematocrit
6%
Adipokine
6%
Transaminase
6%
Medicine and Dentistry
Exon
31%
Hunter Syndrome
18%
Iduronate 2 Sulfatase
18%
Gaucher's Disease
12%
Leptin
12%
Cross Sectional Study
10%
Prevalence
10%
Silent Mutation
10%
Pediatrics
9%
Symptom
8%
Clinical Feature
7%
Mucopolysaccharidosis
7%
Complementary Feeding
7%
Polyunsaturated Fatty Acid
7%
Allele
7%
Anthropometry
6%
Human Milk
6%
Buccal Swab
6%
Neonate
6%
Acetic Acid Derivative
6%
Galactosamine
6%
Sulfatase
6%
Pyridoxine-Dependent Epilepsy
6%
Persistent Truncus Arteriosus
6%
N Acetylgalactosamine
6%
Morquio Syndrome
6%
Lysine
6%
Apolipoprotein
6%
Exercise
6%
Posttransfusion Hepatitis
6%
Nucleic Acid
6%
Bleeding Disorder
6%
Medical Student
6%
Infancy
6%
Lactation
6%
Systematic Review
6%
Malnutrition
6%
Arachidonic Acid
6%
Shock (Circulatory)
6%
Child Behavior Checklist
6%
Six Minute Walk Test
6%
Dengue Hemorrhagic Fever
6%
Patella Dislocation
6%
Systolic Function
6%
Prospective Study
6%
Checklist
6%
Leptin Receptor
6%
Hepatitis C
6%
Atopic Dermatitis
6%
Gastroesophageal Reflux
6%
