Professor of Pediatrics, Johns Hopkins University School of Medicine

Pediatric Pulmonology

Beryl J. Rosenstein practices Pediatric Pulmonology. He attended Tufts University School of Medicine. Tufts University School of Medicine has a rank of 49 in research and a 52 in primary care He received awards:"Regional Top Doctor". Dr. Beryl J. Rosenstein is also published. He has 100 publications published. The lastest publication: "What is a cystic fibrosis diagnosis?'

Publications

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• Description of a standardized nutrition classification plan and its relation to nutritional outcomes in children with cystic fibrosis.
• Primary snoring and growth failure in a patient with cystic fibrosis.
• Paying the piper: investing in infrastructure for patient safety.
• Dietary supplement use in pediatric patients with cystic fibrosis.
• Calcium kinetics are altered in clinically stable girls with cystic fibrosis.
• Gastric function in children with cystic fibrosis: effect of diet on gastric lipase levels and fat digestion.
• Senior executive adopt-a-work unit: a model for safety improvement.
• Endogenous fecal losses of calcium compromise calcium balance in pancreatic-insufficient girls with cystic fibrosis.
• Nonclassic cystic fibrosis: a clinical conundrum.
• Efficiency of calcium absorption is not compromised in clinically stable prepubertal and pubertal girls with cystic fibrosis.
• Cystic fibrosis diagnosis: new dilemmas for an old disorder.
• Screening for cystic fibrosis.
• 4-methylumbelliferylguanidinobenzoate reactive plasma "protease" in cystic fibrosis is albumin.
• Metastatic calcification in cystic fibrosis. A report of two cases.
• Unexpected diagnosis of cystic fibrosis at autopsy.
• Complications of smallpox vaccination United States 1963. II. Results obtained by four statewide surveys.
• A phase I study of an adeno-associated virus-CFTR gene vector in adult CF patients with mild lung disease.
• Nifedipine inhibits hypoxic pulmonary vasoconstriction during rest and exercise in patients with cystic fibrosis and cor pulmonale.
• Moxalactam-tobramycin-resistant Pseudomonas aeruginosa isolates in patients with cystic fibrosis.
• Pediatric outpatient intravenous rehydration.
• Mucoid Pseudomonas aeruginosa from a patient without cystic fibrosis: implications and review of the literature.
• Misclassification problems in diagnosis-related groups. Cystic fibrosis as an example.
• Use of oral contraceptives in women with cystic fibrosis.
• Television and cystic fibrosis case detection.
• Pneumonia and septicemia due to Pseudomonas cepacia in a patient with cystic fibrosis.
• GLYCOGEN STORAGE DISEASE OF THE HEART IN A NEWBORN INFANT.
• DIARRHEA IN A CHILD WITH A CATECHOLAMINE-SECRETING GANGLIONEUROMA. CASE REPORT AND REVIEW OF THE LITERATUTE.
• Salmonellosis in infants and children.
• Accuracy of throat cultures processed in physicians'' offices.
• Incidence of distal intestinal obstruction syndrome in cystic fibrosis.
• Cystic fibrosis: diagnostic considerations.
• Patient safety: a team effort at Johns Hopkins Hospital.
• Congenital renal abnormalities in infants with in utero cocaine exposure.
• Outcomes of emergency room treatment of children with asthma.
• Cystic fibrosis presenting with the meconium plug syndrome.
• Diagnostic delay in Duchenne s muscular dystrophy and cystic fibrosis.
• Differential pathology of nasal polyps in cystic fibrosis and atopy.
• Misdiagnosis of cystic fibrosis. Need for continuing follow-up and reevaluation.
• ABH secretor status in cystic fibrosis--a negative report.
• Cystic fibrosis. Problems encountered with sweat testing.
• Factors involved in treatment failures following oral penicillin therapy of streptococcal pharyngitis.
• Incidence of meconium abnormalities in newborn infants with cystic fibrosis.
• Prolonged obstructive jaundice and giant cell hepatitis in an infant with cystic fibrosis.
• Iodide-induced hypothyroidism without a goiter in an infant with cystic fibrosis.
• Dermatitis as a presenting sign of cystic fibrosis.
• Cystic fibrosis in adults: delayed diagnosis in three siblings.
• A double-blind controlled trial of anti-Pseudomonas chemotherapy of acute respiratory exacerbations in patients with cystic fibrosis.
• Bilateral maxillary sinus mucoceles in an infant with cystic fibrosis.
• Diagnosis of cystic fibrosis during adolescence.
• Lysozyme activity in cystic fibrosis.
• A controlled trial of long-term bronchodilator therapy in cystic fibrosis.
• Newborn identification. Compliance with AAP guidelines for perinatal care.
• Risks of alternate-day prednisone in patients with cystic fibrosis.
• Sweat sodium and chloride values.
• Peptic ulcer disease in cystic fibrosis: an unusual occurrence in black adolescents.
• Prenatal care and drug use in pregnant women.
• The cause of rectal prolapse in children.
• Effect of pancreatic enzyme supplements on iron absorption.
• Passive smoking among children with chronic respiratory disease.
• Mycobacterium avium complex in a patient with cystic fibrosis: disease vs. colonization.
• Effect of aerosolized recombinant human DNase on exacerbations of respiratory symptoms and on pulmonary function in patients with cystic fibrosis. The Pulmozyme Study ...
• Infection prevention promotion program based on the PRECEDE model: improving hand hygiene behaviors among healthcare personnel.
• Prognosis in cystic fibrosis.
• Genotype-phenotype correlations in cystic fibrosis.
• Infant health care utilization predicted by pattern of prenatal care.
• Age-related abnormalities of circulating polyamines and diamine oxidase activity in cystic fibrosis heterozygotes and homozygotes.
• Identification of the major 4-methylumbelliferyl p-guanidinobenzoate-hydrolyzing plasma protein in cystic fibrosis: implication for intrauterine and heterozygote detec...
• Radioaerosol assessment of lung improvement in cystic fibrosis patients treated for acute pulmonary exacerbations.
• Flexible prescription assistance program for patients with cystic fibrosis.
• Airway hyperreactivity in cystic fibrosis. Clinical correlates and possible effects on the course of the disease.
• Homogeneity of bronchopulmonary distribution of 99mTc aerosol in normal subjects and in cystic fibrosis patients.
• What is a cystic fibrosis diagnosis?
• Noninvasive evaluation of ventricular function in cystic fibrosis.
• Effect of rhDNase on airflow obstruction and mucociliary clearance in cystic fibrosis.
• False-positive results of genetic testing in cystic fibrosis.
• Correlation of intestinal lactulose permeability with exocrine pancreatic dysfunction.
• CFTR nonsense mutations G542X and W1282X associated with severe reduction of CFTR mRNA in nasal epithelial cells.
• The Johns Hopkins Hospital: identifying and addressing risks and safety issues.
• A multicenter study of alternate-day prednisone therapy in patients with cystic fibrosis. Cystic Fibrosis Foundation Prednisone Trial Group.
• Analysis of DNA polymorphism haplotypes linked to the cystic fibrosis locus in North American black and Caucasian families supports the existence of multiple mutations...
• Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease.
• Analysis of four diverse population groups indicates that a subset of cystic fibrosis mutations occur in common among Caucasians.
• A cluster of cystic fibrosis mutations in the first nucleotide-binding fold of the cystic fibrosis conductance regulator protein.
• Identification of common cystic fibrosis mutations in African-Americans with cystic fibrosis increases the detection rate to 75%.
• Identification of a novel nonsense mutation (L88X) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene in a native Korean cystic fibrosis chromos...
• Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508...
• Differences in expression of cystic fibrosis in blacks and whites.
• Risk of persistent growth impairment after alternate-day prednisone treatment in children with cystic fibrosis.
• Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of ...
• Calcium acquisition rates do not support age-appropriate gains in total body bone mineral content in prepuberty and late puberty in girls with cystic fibrosis.
• Comparison of the clinical manifestations of cystic fibrosis in black and white patients.
• The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel.
• Current treatment recommendations for correcting vitamin D deficiency in pediatric patients with cystic fibrosis are inadequate.
• Evaluation of the culture of safety: survey of clinicians and managers in an academic medical center.
• Variants in mannose-binding lectin and tumour necrosis factor alpha affect survival in cystic fibrosis.
• Ciprofloxacin-induced renal insufficiency in cystic fibrosis.
• Guidelines for diagnosis of cystic fibrosis in newborns through older adults: Cystic Fibrosis Foundation consensus report.
• Republished paper: assessing and improving safety culture throughout an academic medical centre: a prospective cohort study.
• Assessing and improving safety culture throughout an academic medical centre: a prospective cohort study.

Schools

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• Tufts University

• Johns Hopkins Hospital

Doctors Specialties

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• Pediatrics
• Pediatric Pulmonology

Accepted Insurances

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Awards

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• Regional Top Doctor

Education

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• Johns Hopkins University
• Tufts University School of Medicine

Hospital

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• Johns Hopkins Hospital

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