Medicine & Life Sciences
Phenylketonurias
100%
caseinomacropeptide
73%
Phenylalanine
68%
Diet
57%
Galactosemias
44%
2-Methylbutyryl-CoA Dehydrogenase Deficiency
37%
Neonatal Screening
34%
Inborn Errors Metabolism
30%
VLCAD deficiency
30%
Propionic Acidemia
29%
Food
28%
Cheese
25%
Maple Syrup Urine Disease
24%
Amino Acids
23%
Galactose
20%
Whey
16%
Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase
16%
3-Hydroxyacyl-CoA Dehydrogenase
15%
Fetal Alcohol Spectrum Disorders
15%
Pregnancy
15%
Nutritional Status
14%
Newborn Infant
14%
Carnitine
13%
Nutritionists
13%
acylcarnitine
13%
Gastrostomy
12%
Child
12%
pegvaliase
12%
Long-chain acyl-CoA dehydrogenase deficiency
12%
Proteins
11%
Vitamin D
11%
Feeding Behavior
11%
Dietary Fiber
11%
Guidelines
10%
Trifunctional Protein Deficiency With Myopathy And Neuropathy
10%
Population
10%
Whey Proteins
10%
Food and Beverages
10%
Biotinidase
9%
Maternal Phenylketonuria
9%
Fabaceae
9%
Mothers
9%
Familial cyclic vomiting syndrome
9%
Medium chain acyl CoA dehydrogenase deficiency
9%
Amish
9%
Protein-Restricted Diet
9%
Methylmalonic acidemia
8%
Isoleucine
8%
Tandem Mass Spectrometry
8%
Enhanced Recovery After Surgery
8%
Chemical Compounds
Acyl-CoA
22%
Phenylalanine
19%
Metabolic
16%
Food
15%
Mutation
13%
Disorder
12%
Galactose
11%
3-Hydroxyacyl-CoA
10%
Beverage Can
9%
Ghrelin
9%
Pharmacological Metabolism
9%
Protein
8%
Plasma
8%