Keyphrases
Urea Cycle Disorders
100%
Newborn Screening
92%
Growth Hormone
56%
Inborn Errors of Metabolism
44%
Glycerol Monostearate
42%
Serine Protease Inhibitor
30%
Growth Hormone-releasing Hormone
27%
Pediatric Patients
22%
Messenger RNA (mRNA)
21%
Phenylbutyrate
21%
Ornithine Transcarbamylase Deficiency
19%
Ammonia Control
18%
Phenylacetic Acid
16%
Insulin-like
16%
Growth Factors
16%
Glutamine
15%
Phenylacetylglutamine
15%
Liver Transplantation
14%
Ammonia
13%
Nuclear Factor
13%
Psychosocial Outcomes
13%
Releasing Hormone
12%
Genomic Research
12%
Homocystinuria
12%
Hormone-responsive
12%
Testicular Development
11%
Rat Liver
11%
Minnesota
11%
Neurofibromatosis Type I
11%
Neurofibromatosis Type 1 (NF-1)
11%
Dehydrogenase Deficiency
11%
Hyperammonemic Crisis
11%
Neonate
11%
Liver
11%
Phenylbutyric Acid
11%
Health Care Services
10%
Metabolic
10%
Growth Hormone Treatment
10%
Adult Patients
10%
Genetic Counseling
10%
Developmental Delay
10%
Inflammation
9%
Insulin-like Growth factor-1
9%
Disease Severity
9%
Medical Management
9%
Homocysteine
9%
Duplication
9%
Pituitary
9%
Intellectual Disability
9%
Growth Failure
9%
Biochemistry, Genetics and Molecular Biology
Newborn Screening
65%
Urea Cycle Disorder
63%
Bovine Somatotropin
38%
Growth Hormone
38%
Serine Protease Inhibitor
24%
Blood Plasma
24%
Inborn Error of Metabolism
21%
Messenger RNA
20%
Ornithine Transcarbamylase Deficiency
20%
Genetics
19%
Glycerol
17%
Genotyping
15%
Information System
14%
Medical Genetics
13%
Glutamine
12%
Exome Sequencing
12%
Pyruvate Dehydrogenase Complex
11%
Pyruvate Dehydrogenase
11%
Acyl-CoA
10%
Genetic Counseling
9%
Clinical Research
9%
Response Element
9%
Gene Expression
9%
Amino Acids
9%
Argininosuccinate Lyase
9%
Autosomal Dominant Inheritance
8%
Genomics
8%
Insulin-Like Growth Factor 1
8%
Hepatocyte
7%
Growth-Hormone-Releasing Hormone
7%
Tandem Mass Spectrometry
7%
Enzyme
7%
Beta Oxidation
7%
Fibroblast
6%
Tyrosine Phosphorylation
6%
Genetic Screening
6%
Transcription
6%
Prevalence
5%
Homocysteine
5%
Inheritance
5%
Acute Phase Response
5%
Arginine
5%
Exon
5%
Allele
5%
Medical Genomics
5%
Lifespan
5%
Missense
5%
Autosomal Recessive Inheritance
5%
Screening
5%
Genetic Disorder
5%
Medicine and Dentistry
Newborn Screening
79%
Disease
42%
Inborn Error of Metabolism
39%
Urea Cycle Disorder
36%
Neonatal Infant
35%
Messenger RNA
12%
Neurofibromatosis Type I
11%
Ornithine Transcarbamylase Deficiency
11%
Clinician
11%
Liver Transplantation
10%
Congenital Malformation
10%
Hypoplasia
10%
Health Outcomes
10%
Genetic Counseling
9%
Diagnosis
9%
Primary Health Care
9%
Phenylketonuria
9%
Screening
8%
Homocysteine
8%
Somatomedin C
8%
Genetic Disorder
8%
Growth Disorder
8%
Pregnancy
7%
Growth Hormone
7%
Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency
7%
Noonan Syndrome
7%
Serine Proteinase Inhibitor
7%
Phenylacetic Acid
7%
Skeleton Malformation
7%
Disease
7%
Diseases
7%
Hypotonia
7%
Early Diagnosis
6%
Genetic Screening
6%
Placenta
6%
Liver Graft
6%
Fatty Acid Oxidation
6%
Developmental Delay
6%
Gene Expression
6%
Neonates
6%
Autosomal Dominant Inheritance
6%
Clinical Feature
6%
Pyruvate Dehydrogenase Complex
5%
Receptor
5%
Fibroblast
5%
Child Health
5%
Methionine
5%
Medicine
5%
Transplantation
5%
Translational Research
5%
