Published in Pediatrics on July 01, 1980
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Randomised controlled trial of an aggressive nutritional regimen in sick very low birthweight infants. Arch Dis Child Fetal Neonatal Ed (1997) 0.95
Pulmonary intravascular lipid in neonatal necropsy specimens. Arch Dis Child (1991) 0.87
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Intravenous lipids for preterm infants: a review. Clin Med Insights Pediatr (2015) 0.76
Transcutaneous application of oil and prevention of essential fatty acid deficiency in preterm infants. Arch Dis Child (1993) 0.75
Parenteral lipids and free radicals in preterm infants. Arch Dis Child (1992) 0.75
Genomic heterogeneity of AIDS retroviral isolates from North America and Zaire. Science (1985) 6.31
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Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkage. Am J Hum Genet (1988) 4.86
Selective trafficking of KNOTTED1 homeodomain protein and its mRNA through plasmodesmata. Science (1995) 4.40
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Glycogen storage disease in adults. Ann Intern Med (1994) 3.58
Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med (1998) 2.57
Failure of a human immunodeficiency virus (HIV) immune globulin to protect chimpanzees against experimental challenge with HIV. Proc Natl Acad Sci U S A (1988) 2.47
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A conceptual model of psychosomatic illness in children. Family organization and family therapy. Arch Gen Psychiatry (1975) 2.31
Gene dosage and suceptibility to insulin-dependent diabetes. Ann Hum Genet (1980) 2.29
A syndrome of congenital hyperinsulinism and hyperammonemia. J Pediatr (1997) 2.15
Cotherapy with recombinant human insulin-like growth factor I and insulin improves glycemic control in type 1 diabetes. RhIGF-I in IDDM Study Group. Diabetes Care (1999) 2.14
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Superoxide-mediated modification of low density lipoprotein by arterial smooth muscle cells. J Clin Invest (1986) 2.01
Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels. Pediatr Res (1983) 1.91
Fasting hypoglycaemia and metabolic acidosis associated with deficiency of hepatic fructose-1,6-diphosphatase activity. Lancet (1970) 1.87
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes (1997) 1.86
Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet (1996) 1.76
Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatr Res (1985) 1.75
The causes of neonatal hypoglycemia. N Engl J Med (1999) 1.68
Acute fatty liver of pregnancy, hemolysis, elevated liver enzymes, and low platelets syndrome, and long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Am J Gastroenterol (1996) 1.66
Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism. J Pediatr (1993) 1.65
Insulin-like growth factor binding protein-1 levels in the diagnosis of hypoglycemia caused by hyperinsulinism. J Pediatr (1997) 1.58
Long-chain acyl coenzyme A dehydrogenase deficiency: an inherited cause of nonketotic hypoglycemia. Pediatr Res (1985) 1.56
Oscillatory patterns in sympathetic neural discharge and cardiovascular variables during orthostatic stimulus. Circulation (2000) 1.55
Linkage-disequilibrium mapping without genotyping. Nat Genet (1998) 1.52
Improved oxygenation and lung compliance with prone positioning of neonates. J Pediatr (1979) 1.51
Genotype and phenotype correlations in 417 children with congenital hyperinsulinism. J Clin Endocrinol Metab (2012) 1.49
Medium-chain acyl-CoA dehydrogenase deficiency. Diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine. N Engl J Med (1988) 1.49
A mobile metabolic crib for infants. Am J Dis Child (1967) 1.48
Dual regulation of insulin-like growth factor binding protein-1 levels by insulin and cortisol during fasting. J Clin Endocrinol Metab (1998) 1.48
Differences in mucosal appearances and in relapse rates in duodenal ulceration treated with sucralfate or cimetidine. Am J Med (1989) 1.43
Sudden neonatal death in carnitine transporter deficiency. J Pediatr (1997) 1.43
Linear gastric emptying of hyperosmolar glucose solutions. J Nucl Med (1991) 1.43
Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome. J Pediatr (2001) 1.42
Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase. J Clin Endocrinol Metab (2001) 1.42
Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. Hepatology (1994) 1.41
Beta cell nesidioblastosis in idiopathic hypoglycemia of infancy. J Pediatr (1971) 1.40
Differentiating benign from malignant solid breast masses: value of shear wave elastography according to lesion stiffness combined with greyscale ultrasound according to BI-RADS classification. Br J Cancer (2012) 1.40
Massive hepatomegaly, steatosis, and secondary plasma carnitine deficiency in an infant with cystic fibrosis. Pediatrics (1989) 1.39
End-of-life confusion in patients with cancer. Oncol Nurs Forum (1998) 1.39
Prevalence, clinical significance, and strain specificity of neutralizing antibody to the human immunodeficiency virus. J Infect Dis (1987) 1.38
Hyperinsulinism in infancy: diagnosis by demonstration of abnormal response to fasting hypoglycemia. Pediatrics (1976) 1.35
Human Curvularia infections. Report of five cases and review of the literature. Diagn Microbiol Infect Dis (1987) 1.34
Glycemic response to glucagon during fasting hypoglycemia: an aid in the diagnosis of hyperinsulinism. J Pediatr (1980) 1.34
Testosterone supplementation improves spatial and verbal memory in healthy older men. Neurology (2001) 1.34
Treatment of laryngotracheobronchitis (croup). Use of intermittent positive-pressure breathing and racemic epinephrine. Am J Dis Child (1975) 1.34
Mitochondrial carnitine-acylcarnitine translocase deficiency presenting as sudden neonatal death. J Pediatr (1997) 1.32
Nervous system in Pompe's disease. Ultrastructure and biochemistry. J Neuropathol Exp Neurol (1971) 1.31
Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder. J Pediatr (1991) 1.30
Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation. J Mol Biol (2001) 1.29
Insulin effects on glucose metabolism, memory, and plasma amyloid precursor protein in Alzheimer's disease differ according to apolipoprotein-E genotype. Ann N Y Acad Sci (2000) 1.27
Decreased synthesis of interleukin-2 (IL-2) in insulin-dependent diabetes mellitus. Diabetes (1984) 1.25
The practicality of chronic hepatic artery infusion therapy of primary and metastatic hepatic malignancies: ten-year results of 124 patients in a prospective protocol. Cancer (1981) 1.22
Major and minor depression in Alzheimer's disease: prevalence and impact. J Neuropsychiatry Clin Neurosci (1997) 1.21
The early partial remission of juvenile diabetes mellitus. The roles of insulin and growth hormone. J Pediatr (1967) 1.21
Difluorodeoxycytidine (dFdC)--gemcitabine: a phase I study. Invest New Drugs (1992) 1.21
Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts. N Engl J Med (1988) 1.19
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Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene. Nat Genet (1994) 1.18
New antimalarial treatment for KwaZulu-Natal. S Afr Med J (2001) 1.17
Awake apnea associated with gastroesophageal reflux: a specific clinical syndrome. J Pediatr (1984) 1.17
Relationship between unusual hepatic acyl coenzyme A profiles and the pathogenesis of Reye syndrome. J Clin Invest (1988) 1.16
Determination of the equilibrium constants of associating protein systems. 3. Evaluation of the weight fraction of monomer from the weight-average partition coefficient (application to bovine liver glutamate dehydrogenase). Biochemistry (1969) 1.15
Disorders of glutamate metabolism. Ment Retard Dev Disabil Res Rev (2001) 1.15
Meticulous control of diabetes during organogenesis prevents congenital lumbosacral defects in rats. Diabetes (1981) 1.14
'Competition' among employers offering health insurance. J Health Econ (2000) 1.14
Hyperinsulinism in infants and children: diagnosis and therapy. Adv Pediatr (1976) 1.14
Chronic severe constipation. Prospective motility studies in 25 consecutive patients. Gastroenterology (1987) 1.13
Association between attention deficit-hyperactivity disorder and learning disorders. J Learn Disabil (1991) 1.13
Hypertrichosis lanuginosa associated with diazoxide therapy in prepubertal children: a clinicopathologic study. Ann N Y Acad Sci (1968) 1.13
Congenital hyperinsulinism and the surgeon: lessons learned over 35 years. J Pediatr Surg (1999) 1.13
Genetic heterogeneity in familial hyperinsulinism. Hum Mol Genet (1998) 1.12
Medium-chain and long-chain acyl CoA dehydrogenase deficiency: clinical, pathologic and ultrastructural differentiation from Reye's syndrome. Hepatology (1987) 1.11
Persistent pulmonary hypertension in the neonate: diagnosis and management. J Pediatr (1983) 1.11
Prevalence and type of psychiatric disorder and developmental disorders in three speech and language groups. J Commun Disord (1987) 1.11
Physiologic implications of two different heat shields for infants under radiant warmers. J Pediatr (1982) 1.11
Rapid gastric emptying of an oral glucose solution in type 2 diabetic patients. J Nucl Med (1992) 1.09
Effect of tri-iodothyronine replacement on the metabolic and pituitary responses to starvation. N Engl J Med (1979) 1.08
Molecular classification of synovial sarcomas, leiomyosarcomas and malignant fibrous histiocytomas by gene expression profiling. Br J Cancer (2003) 1.08
Detection of HIV antigen and specific antibodies to HIV core and envelope proteins in sera of patients with HIV infection. Blood (1987) 1.07
Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. Diabetes (2001) 1.07
Pulmonary physiotherapy in neonates: physiologic changes and respiratory management. J Pediatr (1978) 1.07