Medicine and Dentistry
Water-Electrolyte Imbalance
100%
Inborn Error of Metabolism
100%
Molecular Diagnosis
100%
Diseases
78%
Patient
34%
Incidence
17%
Carbohydrate
17%
Phenylketonuria
17%
Propionic Acidemia
17%
Isovaleric Acidemia
17%
Hospital
17%
Lysosomal Storage Disease
17%
Vermiform Appendix
17%
Fatty Acid Oxidation
8%
Newborn Death
8%
Biological Marker
8%
Mass Spectrum
8%
Age
8%
Prevalence
8%
Population
8%
Genetic Screening
8%
Analysis
8%
Neonates
8%
Maple Syrup Urine Disease
8%
Neonatal Infant
8%
Amino Acid
8%
Storage Disease
8%
Child
8%
Autosomal Recessive Disorder
8%
Family
8%
Lactic Acidosis
8%
Child Death
8%
Homocystinuria
8%
Consanguinity
8%
Newborn Screening
8%
Acid
8%
Screening
8%
Female
8%
Job
8%
Male
8%
Phenotype
8%
Metabolism
8%
Disorders of Mitochondrial Functions
8%
Gene
8%
Fatty Acid
8%
Biochemistry, Genetics and Molecular Biology
Inborn Error of Metabolism
100%
Mutation
57%
Incidence
19%
Carbohydrate
19%
Phenylketonuria
19%
Metabolic Disorder
19%
Newborn Screening
9%
Population
9%
Propionic Acidemia
9%
Consanguinity
9%
Genetic Screening
9%
Nested Gene
9%
Amino Acids
9%
Spectroscopy
9%
Mental Retardation
9%
Beta Oxidation
9%
Screening
9%
Urea Cycle Disorder
9%
Metabolic Pathway
9%
Age
9%
Lysosomal Storage Disease
9%
Phenotype
9%
Homocystinuria
9%
Urea Cycle
9%
Sample
9%
Krabbe Disease
9%
Medical Genetics
9%
Prevalence
9%
Mitochondrial Disorder
9%
Fatty Acid
9%
Retrospective Study
9%