2009 Subject Index

21-hydroxylase, congenital, 11622q11.2 deletion syndrome, 15125OHD, 266Adiponectin, 233Adiponectin, 262Adolescence, 205Adolescent morbidity, 188Adolescents, 181Adrenal hyperplasia, 116Alström syndrome, 278Androgen, 256Aromatase, 256ATPase activity, 157Child, 278Children and adolescents, 136Children, 181Children, 233Chorionic gonadotropin, 281Clinical findings, 209Congenital, 244Cord, 266Curve, 129CYP21A2 gene, 116Detemir, 181Diabetic ketoacidosis, 144Diagnosis, 270EEC syndrome, 252Erythrocyte Na+,K+-, 157Estrogen, 256Femur involvement, 194Genotype, 116Glargine, 181Glucagon-like peptide 1, 144Glucagon-like peptide 2, 144Gonadotropin-releasing, 256Hormone agonists, 256Growth hormone deficiency, 248Growth hormone, 205Growth hormone, 205Growth, 105Growth retardation, 157Hemoglobin A1c, 227Hepatoblastoma, 281Hypertension, 175Hypocalcemia, 151Hypoparathyroidism, 151Hypothalamo-pituitary insufficiency, 252Hypothyroidism, 197Hypothyroidism, 244Hypothyroidism, 275Idiopathic short stature, 105Inhibitors, 256Insulin-like growth factor, 105Investigation, 209Iodine overload, 275Leptin, 175Melnick-Needles syndrome, 248Metabolic rates, 157Metabolic syndrome, 233, 278Metabolic, 205Microalbuminuria, 136Mother, 266Mutation, 116Neonate, 197Neonate, 275New onset, 227Newborn, 266Norepinephrine, 175NPH, 181Nutrient intake, 157Nutritional growth retardation (NGR), 157Obesity, 175Obesity, 233Osteoma cutis, 244PCOS, 188Percentile, 129Phenotype, 116Polycystic ovary syndrome, 188Precocious puberty, 164Premature pubarche, 164Premature thelarche, 164Pseudohypoparathyroidism, 244Puberty, 281Radiography, 194Reproductive age women, 266Rickets, 262Short stature, 157Skeletal dysplasia, 270Skeletal survey, 270Sludge, 197Steroid, 209Sympathetic nervous system, 175Transition, 205Treatment, 262Type 1 diabetes mellitus, 144Type 1 diabetes, 136Type 1 diabetes, 227Type 2 diabetes, 227Vitamin D, 262Weight, height, 129Weismann-Netter-Stuhl syndrome, 194