Published in J Pediatr on February 01, 1977
Management of patients with congenital hypothyroidism. Br Med J (Clin Res Ed) (1985) 1.14
Serum thyroxine and thyroid stimulating hormone concentrations after treatment of congenital hypothyroidism. Arch Dis Child (1988) 1.09
Maintenance requirements of L-thyroxine in the treatment of hypothyroidism. West J Med (1984) 1.09
Increased plasma thyroid stimulating hormone in treated congenital hypothyroidism: relation to severity of hypothyroidism, plasma thyroid hormone status, and daily dose of thyroxine. Arch Dis Child (1993) 1.02
Monitoring TSH concentrations during treatment for congenital hypothyroidism. Arch Dis Child (1991) 0.93
Reappraisal of thyroxine treatment in primary hypothyroidism. Arch Dis Child (1990) 0.88
Partial end organ resistance to thyroid hormone in congenital hypothyroidism. Postgrad Med J (1981) 0.75
Phenylalaninemia. Pediatr Clin North Am (1968) 1.53
Severe insulin-induced hypoglycemia associated with deficiencies in the release of counterregulatory hormones. N Engl J Med (1981) 1.30
Observations on the coexistence of methylmalonic acidemia and glycinemia. J Pediatr (1969) 1.20
Congenital familial sensory neuropathy with anhidrosis. J Pediatr (1966) 1.18
Hereditary multicentric osteolysis with recessive transmission: a new syndrome. J Pediatr (1969) 1.17
Role of the thymus in humoral immunity. Lancet (1969) 1.15
Prospective study of maple-syrup-urine disease for the first four days of life. N Engl J Med (1982) 1.04
Cerebral edema causing death in children with maple syrup urine disease. J Pediatr (1991) 1.04
Factors predicting cerebral edema in young children with diabetic ketoacidosis and new onset type I diabetes. Acta Paediatr (1997) 1.01
Fanconi's anemia with growth hormone deficiency. J Pediatr (1971) 1.01
A novel mutation of the adrenocorticotropin receptor (ACTH-R) gene in a family with the syndrome of isolated glucocorticoid deficiency, but no ACTH-R abnormalities in two families with the triple A syndrome. J Clin Endocrinol Metab (1995) 0.93
Cloning and expression of mutations demonstrating intragenic complementation in mut0 methylmalonic aciduria. J Clin Invest (1994) 0.90
Normal lymphocyte transfer (NLT) test: negative response in a patient with congenital absence of the thymus. Transplantation (1967) 0.89
Human T-lymphotropic virus type 1 peptides in chimeric and multivalent constructs with promiscuous T-cell epitopes enhance immunogenicity and overcome genetic restriction. J Virol (1995) 0.88
Effects of glucagon on plasma amino acids. J Clin Invest (1984) 0.88
Substitution of arginine-839 by cysteine or histidine in the androgen receptor causes different receptor phenotypes in cultured cells and coordinate degrees of clinical androgen resistance. J Clin Invest (1994) 0.85
Assessment of stature in children with orofacial clefting. MCN Am J Matern Child Nurs (1999) 0.84
Congenital absence of the thymus. Am J Roentgenol Radium Ther Nucl Med (1968) 0.84
Use of tissue-specific promoters in the regulation of aromatase cytochrome P450 gene expression in human testicular and ovarian sex cord tumors, as well as in normal fetal and adult gonads. J Clin Endocrinol Metab (1993) 0.83
Glucagon deficiency and hyperaminoacidemia after total pancreatectomy. J Clin Invest (1980) 0.83
Use of tissue-specific promoters in the regulation of aromatase cytochrome P450 gene expression in human testicular and ovarian sex cord tumors, as well as in normal fetal and adult gonads. J Clin Endocrinol Metab (1994) 0.83
Effects of growth hormone administration in pediatric renal allograft recipients. Pediatr Nephrol (1992) 0.82
The encephalomyocarditis virus 3C protease is a substrate for the ubiquitin-mediated proteolytic system. J Biol Chem (1994) 0.82
Picture of the month. Dyschondrosteosis (Leri-Weil syndrome, Leri's pleonostenosis). Am J Dis Child (1971) 0.82
Role of glucagon in disposal of an amino acid load. Am J Physiol (1990) 0.82
Engineered topographic determinants with alpha beta, beta alpha beta, and beta alpha beta alpha topologies show high affinity binding to native protein antigen (lactate dehydrogenase-C4). J Biol Chem (1993) 0.81
[The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases]. Ann Genet (1967) 0.81
Clinical evaluation of the anorexic activity and safety of 42-548 in children. Report of a clinical trial. Clin Pediatr (Phila) (1973) 0.81
Inhibition of thyrotropin releasing hormone-mediated secretion of thyrotropin by human growth hormone. J Clin Endocrinol Metab (1973) 0.81
Action of human growth hormone (hGH) on extrathyroidal conversion of thyroxine (T4) to triiodothyronine (T3) in children with hypopituitarism. Pediatr Res (1981) 0.81
Focal dermal hypoplasia symdrome in a male. Clin Genet (1975) 0.80
An islet cell carcinoma containing glucagon and insulin. Chronic glucagon excess and glucose homeostasis. Diabetes (1977) 0.80
Prenatal treatment of thyrotoxicosis to prevent intrauterine growth retardation. Obstet Gynecol (1982) 0.79
Immunogenicity and conformational properties of an N-linked glycosylated peptide epitope of human T-lymphotropic virus type 1 (HTLV-I). Biomed Pept Proteins Nucleic Acids (1995) 0.78
Disproportionate suppression of dehydroepiandrosterone sulfate (DHEAS) in treated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Pediatr Res (1983) 0.78
The association of aniridia, Wilms's tumor, and genital abnormalities. Trans Am Ophthalmol Soc (1965) 0.78
Cryptorchidism: a pediatrician's view. Pediatr Clin North Am (1987) 0.78
Effect of growth hormone on mitochondrial protein synthesis. J Biol Chem (1973) 0.77
Maldescent of the thymus. Pediatr Pathol (1994) 0.77
Distribution of 3 H-acetyl human growth hormone in subcellular fractions of rat liver. Biochem Med (1970) 0.76
The association of aniridia, Wilms' tumor, and genital abnormalities. Arch Ophthalmol (1966) 0.76
Kinetics of uptake and subcellular distribution of human growth hormone in liver slices. Biochem Med (1973) 0.76
Childhood obesity--to treat or not to treat. Med Times (1971) 0.76
Nonbinding inhibitory antiinsulin receptor antibodies. A new type of autoantibodies in human diabetes. J Clin Invest (1988) 0.75
Idiopathic hypercalcemia of infancy: optic atrophy and other ocular changes. Trans Am Acad Ophthalmol Otolaryngol (1966) 0.75
The association of congenital malformations and malignant tumors in infants and children. Ann Clin Lab Sci (1974) 0.75
Glycosylation-dependent peptide antigenic determinants of env gp46 HTLV-1. Leukemia (1995) 0.75
Primary hypothyroidism in cystinosis. J Pediatr (1977) 0.75
Sporadic aniridia and Wilms' tumor. Am J Ophthalmol (1969) 0.75
Evaluation of screening tests for urinary mucopolysaccharides. Pediatrics (1973) 0.75
Human growth hormone reaction with tetranitromethane. Res Commun Chem Pathol Pharmacol (1972) 0.75
Inactivation of microsomal glucose-6-phosphatase by pyridoxal-5'-phosphate. Biochem Biophys Res Commun (1971) 0.75
46,XY monozygotic twins with discordant sex phenotype. Fertil Steril (2000) 0.75
A complication of phototherapy in the newborn: the "bronze baby". Clin Pediatr (Phila) (1973) 0.75
Activation of microsomal glucose-6-phosphatase and associated pyrophosphatase and pyrophosphate-glucose phosphotransferase activities of human liver by aluminum oxide. Biochem Med (1971) 0.75
Allergic rhinitis and constitutional growth delay. Ann Allergy (1972) 0.75
Inheritance of cryptorchidism. Pediatrics (1976) 0.75
The molecular weights of twelve apolipoprotein(a) variants, determined using haptoglobin 2-2 polymer molecular weight standards. Appl Theor Electrophor (1993) 0.75
A potential danger of oral chlorpropamide therapy: impaired excretion of a water load. J Clin Endocrinol Metab (1972) 0.75
Presentation of Howland award to Waldo E. Nelsen. Pediatr Res (1972) 0.75