Published in J Pediatr on February 01, 1986
Pseudomonas cepacia infection in cystic fibrosis: an emerging problem. J Pediatr (1984) 9.61
Management of asthma: a consensus statement. Arch Dis Child (1989) 7.04
The Neutron Pile as a Tool in Quantitative Analysis; The Gallium and Palladium Content of Iron Meteorites. Science (1949) 6.35
Prediction of mortality in patients with cystic fibrosis. N Engl J Med (1992) 5.46
The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508). N Engl J Med (1990) 4.70
A comparison of survival, growth, and pulmonary function in patients with cystic fibrosis in Boston and Toronto. J Clin Epidemiol (1988) 4.41
The effect of full-time faculty hospitalists on the efficiency of care at a community teaching hospital. Ann Intern Med (1998) 4.03
Quantitative assessment of pulmonary hypertension in patients with tricuspid regurgitation using continuous wave Doppler ultrasound. J Am Coll Cardiol (1985) 3.50
Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis. J Pediatr (1997) 3.38
Classification of suicidal behaviors: I. Quantifying intent and medical lethality. Am J Psychiatry (1975) 2.89
Identification of a mutation at codon 65 in the IKKK motif of reverse transcriptase that encodes human immunodeficiency virus resistance to 2',3'-dideoxycytidine and 2',3'-dideoxy-3'-thiacytidine. Antimicrob Agents Chemother (1994) 2.81
Bronchial reactivity in cystic fibrosis. Pediatrics (1978) 2.70
Standards of pulmonary function in children. Am Rev Respir Dis (1969) 2.56
Sustained-release theophylline for childhood asthma: evidence for circadian variation of theophylline pharmacokinetics. J Pediatr (1981) 2.41
Modification of human cytomegalovirus tropism through propagation in vitro is associated with changes in the viral genome. J Gen Virol (1999) 2.33
Pulmonary function abnormalities in symptom-free children after bronchiolitis. Pediatrics (1977) 2.32
Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa. J Pediatr (1990) 2.28
Association of respiratory viral infections with pulmonary deterioration in patients with cystic fibrosis. N Engl J Med (1984) 2.22
Radiation-induced optic neuropathy: a magnetic resonance imaging study. J Neurosurg (1991) 2.07
High-dose versus low-dose intravenous immunoglobulin in hypogammaglobulinaemia and chronic lung disease. Lancet (1987) 2.05
Five- to seven-year course of pulmonary function in cystic fibrosis. Am Rev Respir Dis (1976) 2.03
Pulmonary function and bronchial hyperreactivity in long-term survivors of bronchopulmonary dysplasia. Pediatrics (1981) 2.00
Well-established nucleon resonances revisited by double-polarization measurements. Phys Rev Lett (2012) 1.99
Ultrastructure of airways in children with asthma. Histopathology (1978) 1.97
Lactic and Malic Dehydrogenases in Human Spermatozoa. Science (1963) 1.81
Hepatic abscess and cystic fibrosis. Postgrad Med J (1988) 1.77
Microvillus inclusion disease: an inherited defect of brush-border assembly and differentiation. N Engl J Med (1989) 1.77
Role of conventional physiotherapy in cystic fibrosis. J Pediatr (1988) 1.75
Tumour hypoxia imaging with [18F]FAZA PET in head and neck cancer patients: a pilot study. Eur J Nucl Med Mol Imaging (2007) 1.70
Removal of nasal foreign bodies in children. Clin Pediatr (Phila) (1993) 1.70
Correlation of sweat chloride concentration with classes of the cystic fibrosis transmembrane conductance regulator gene mutations. J Pediatr (1995) 1.70
Two-year results of a randomized controlled trial of a health promotion program in a retiree population: the Bank of America Study. Am J Med (1993) 1.67
Toronto street youth and HIV/AIDS: prevalence, demographics, and risks. J Adolesc Health (1999) 1.66
DNA marker haplotype association with pancreatic sufficiency in cystic fibrosis. Am J Hum Genet (1989) 1.66
Diabetes mellitus in patients with cystic fibrosis: effect on survival. Pediatrics (1990) 1.65
Improved respiratory prognosis in patients with cystic fibrosis with normal fat absorption. J Pediatr (1982) 1.64
Studies on breath methane: the effect of ethnic origins and lactulose. Gut (1980) 1.63
The right to effective education. Behav Anal (1991) 1.62
Increased incidence of bronchial reactivity in children with a history of bronchiolitis. J Pediatr (1981) 1.62
Ceftazidime alone and in combination in patients with cystic fibrosis: lack of efficacy in treatment of severe respiratory infections caused by Pseudomonas cepacia. J Antimicrob Chemother (1983) 1.60
Quantitative protein analysis from formalin-fixed tissues: implications for translational clinical research and nanoscale molecular diagnosis. J Pathol (2007) 1.60
Clinical and physiological assessment of asthmatic children treated with beclomethasone dipropionate. J Allergy Clin Immunol (1976) 1.59
Multilocus genotyping of Giardia duodenalis reveals striking differences between assemblages A and B. Int J Parasitol (2008) 1.59
Transit time analysis of the forced expiratory vital capacity in cystic fibrosis. Am Rev Respir Dis (1976) 1.58
Infertility in female rabbits immunized with lactate dehydrogenase X. Science (1973) 1.57
Efficacy of frequent nebulized ipratropium bromide added to frequent high-dose albuterol therapy in severe childhood asthma. J Pediatr (1995) 1.56
Severe acute asthma in a pediatric intensive care unit: six years' experience. Pediatrics (1989) 1.54
Volume of isoflow. A new test in detection of mild abnormalities of lung mechanics. Am Rev Respir Dis (1974) 1.53
Benefit of intravenous IgG replacement in hypogammaglobulinemic patients with chronic sinopulmonary disease. Am J Med (1985) 1.52
Pulmonary function in children with asthma at acute attack and symptom-free status. Am Rev Respir Dis (1969) 1.52
The approach to chronic cough in childhood. Ann Allergy (1988) 1.51
High-dose pancreatic-enzyme supplements and fibrosing colonopathy in children with cystic fibrosis. N Engl J Med (1997) 1.51
Mucociliary tracheal transport rates in man. J Appl Physiol (1975) 1.50
Effect of cimetidine and sodium bicarbonate on pancreatic replacement therapy in cystic fibrosis. Gut (1980) 1.50
Acute pancreatitis in childhood. J Pediatr (1988) 1.49
Shwachman syndrome: phenotypic manifestations of sibling sets and isolated cases in a large patient cohort are similar. J Pediatr (1999) 1.47
Lung function in children following repair of tracheoesophageal fistula. J Pediatr (1979) 1.46
Airway closure in children. J Appl Physiol (1972) 1.45
Hypoalbuminemia at initial examination in patients with cystic fibrosis. J Pediatr (1989) 1.45
A position paper of the North American Society for Pediatric Gastroenterology and Nutrition. Pediatric gastroenterology Workforce Survey and future supply and demand. J Pediatr Gastroenterol Nutr (1998) 1.45
Bile acid secretion in cystic fibrosis: evidence for a defect unrelated to fat malabsorption. Gut (1986) 1.44
Childhood asthma: a rational approach to treatment. Ann Allergy (1990) 1.44
Spacers in childhood asthma--is there one for all occasions? Ann Allergy (1990) 1.43
Maximal expiratory flows generated by rapid chest compression following end-inspiratory occlusion or expiratory clamping in young children. Eur Respir J (1995) 1.41
Serological detection of a cell-surface antigen specified by the T (brachyury) mutant gene in the house mouse. Proc Natl Acad Sci U S A (1972) 1.41
Amino acid composition and properties of crystalline lactate dehydrogenase X from mouse testes. J Biol Chem (1972) 1.41
Photoproduction of eta-mesic 3He. Phys Rev Lett (2004) 1.39
Effect of albumin on results for the free-thyroxin index as estimated by the total T4/T3 uptake ratio. Clin Chem (1989) 1.39
Biomedical support options for today and tomorrow. Interview by Bill Betts. Biomed Instrum Technol (1998) 1.39
Molecular pathogenesis of Epstein-Barr virus associated posttransplant lymphomas: new insights through latent membrane protein 1 fingerprinting. Transplantation (2001) 1.39
The patient with asymptomatic advanced renal failure--obstructive uropathy caused by inflammatory abdominal aortic aneurysm. Nephrol Dial Transplant (1998) 1.38
Transcutaneous monitoring of oxygenation: what is normal? J Pediatr (1986) 1.37
Monitoring of mixed venous oxygen saturation and pressure from biosensors in the right ventricle. A 24 hour study in patients with heart failure. Eur Heart J (1995) 1.37
Clinical and genetic comparisons of patients with cystic fibrosis, with or without meconium ileus. J Pediatr (1989) 1.37
Changes in ventilation and chest wall mechanics during sleep in normal adolescents. J Appl Physiol Respir Environ Exerc Physiol (1981) 1.36
Spacing devices and metered-dose inhalers in childhood asthma. J Pediatr (1985) 1.35
Sodium cromoglycate-induced changes in the dose-response curve of inhaled methacholine and histamine in asthmatic children. Am Rev Respir Dis (1979) 1.35
Age-related alterations of immunoreactive pancreatic cationic trypsinogen in sera from cystic fibrosis patients with and without pancreatic insufficiency. Pediatr Res (1986) 1.34
Intermittent positive pressure respiration as a treatment in severe respiratory distress syndrome. Arch Dis Child (1965) 1.34
Pregnancy and cystic fibrosis. Obstet Gynecol (1991) 1.33
The response to exercise in normal and asthmatic children. J Pediatr (1978) 1.32
Long-term effects of inhaled tobramycin in patients with cystic fibrosis colonized with Pseudomonas aeruginosa. Pediatr Pulmonol (1989) 1.31
High-versus low-dose, frequently administered, nebulized albuterol in children with severe, acute asthma. Pediatrics (1989) 1.30
Pulmonary function in infants and children following the acute neonatal respiratory distress syndrome. Bull Physiopathol Respir (Nancy) (1974) 1.30
Effects of long-term nutritional rehabilitation on body composition and clinical status in malnourished children and adolescents with cystic fibrosis. J Pediatr (1985) 1.30
Selective active site inhibitors of human lactate dehydrogenases A4, B4, and C4. Biochem Pharmacol (2001) 1.30
Efficacy of albuterol administered by nebulizer versus spacer device in children with acute asthma. J Pediatr (1993) 1.30
Satisfaction with continuous glucose monitoring in adults and youths with Type 1 diabetes. Diabet Med (2011) 1.29
Early detection of pulmonary function abnormalities in cystic fibrosis. Pediatrics (1972) 1.29
Recommendations for management of liver and biliary tract disease in cystic fibrosis. Cystic Fibrosis Foundation Hepatobiliary Disease Consensus Group. J Pediatr Gastroenterol Nutr (1999) 1.28
Treatment of distal intestinal obstruction syndrome in cystic fibrosis with a balanced intestinal lavage solution. Lancet (1986) 1.28
Pathology of pancreatic and intestinal disorders in cystic fibrosis. J R Soc Med (1998) 1.28
Skeletal phenotype in patients with Shwachman-Diamond syndrome and mutations in SBDS. Clin Genet (2004) 1.27
Acute asthma: observations regarding the management of a pediatric emergency room. Pediatrics (1989) 1.27
Ventilatory muscle endurance training in normal subjects and patients with cystic fibrosis. Am Rev Respir Dis (1977) 1.26
Evidence for a primary defect of pancreatic HCO3-secretion in cystic fibrosis. Pediatr Res (1982) 1.26
Alpha 1 antitrypsin deficiency in association with both cirrhosis and chronic obstructive lung disease in two sibs. Am J Med (1973) 1.26
Spinal subdural hematoma: a rare cause of recurrent postoperative radiculopathy. J Spinal Disord (1993) 1.26
Uncertainty in the diagnosis of cystic fibrosis: possible role of in vivo nasal potential difference measurements. J Pediatr (1998) 1.26