Biochemistry, Genetics and Molecular Biology
Genetics
44%
Congenital Hyperinsulinism
43%
Genetic Screening
32%
Proband
29%
Prevalence
28%
Genotyping
28%
Insulin Release
26%
Germ Cell
25%
Germline
25%
ACVRL1
22%
ABCC8
18%
Gene Expression
17%
Germline Mutation
16%
Mosaicism
16%
Diazoxide
16%
Phosphotransferase
15%
Kinase
15%
Gene Mutation
14%
Molecular Genetics
13%
Insulin Resistance
13%
Infancy
12%
Single-Nucleotide Polymorphism
11%
Cohort Study
11%
Rickets
11%
Haplotype
11%
Glucokinase
11%
Next Generation Sequencing
11%
Exon
10%
Genetic Disorder
10%
Microarrays
9%
Genetic Heterogeneity
9%
Skeletal Muscle
9%
Adenosine Triphosphate
9%
Exome Sequencing
9%
Missense
9%
Whole Genome Sequencing
9%
Serine Protease Inhibitor
9%
Arginine
9%
Autosomal Recessive Inheritance
9%
Secretory Pathway
8%
Blood Level
8%
Dideoxynucleotide Sequencing
8%
Genetic Divergence
8%
Potassium Channel
7%
Autosomal Dominant Inheritance
7%
Missense Mutation
7%
Endoglin
7%
Protein Sequencing
7%
Trypsinogen
6%
Body Height
6%
Medicine and Dentistry
Congenital Hyperinsulinism
100%
Hyperinsulinemic Hypoglycemia
43%
Disease
41%
Hereditary Hemorrhagic Telangiectasia
22%
Surgery
21%
Hypoglycemia
19%
Cohort Analysis
16%
Polycystic Ovary Syndrome
16%
Diabetes
16%
Gene Expression
13%
Octreotide
13%
Beta Cell
12%
Mosaicism
12%
Diazoxide
12%
Adenosine Triphosphate
12%
Blood Glucose
12%
Hyperinsulinism
11%
DOPA
11%
Patient Referral
11%
Peroperative Echography
11%
Hydroxybutyric Acid
11%
Potassium Channel
11%
Hypophosphatemic Rickets
11%
Ketoacidosis
11%
Genetic Analysis
11%
Genetic Screening
10%
Positron Emission Tomography-Computed Tomography
9%
Vitamin D
9%
Insulin Release
9%
Beckwith Wiedemann Syndrome
9%
Nesidioblastosis
9%
Maturity Onset Diabetes of the Young
9%
Insulin Resistance
8%
Hearing Impairment
8%
Adenosine Triphosphate Sensitive Potassium Channel
8%
Diagnosis
7%
In Vitro
7%
Pancreatic Islet
7%
Skeletal Muscle
7%
Prevalence
6%
Pulmonary Arteriovenous Fistula
6%
Single Nucleotide Polymorphism
6%
X Linked Hypophosphatemic Rickets
6%
Multiple Endocrine Neoplasia Type I
6%
Uniparental Disomy
6%
Peutz Jeghers Syndrome
6%
Pediatrics
6%
Autosomal Dominant Inheritance
6%
Fluorine-18
5%
Epileptic Absence
5%
