Johns Hopkins Hospital
Pediatric Pulmonology
Dr. Peter J. Mogayzel, MD
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Doctor Peter J. Mogayzel, MD works in the field of Pediatric Pulmonology. He researched medicine at Boston University School of Medicine. Boston University School of Medicine is ranked 30 in research and 52 in primary care medicine He over the years received 2 awards: "Fellow (FAAP)" and "Fellow (FACP)". Dr. Peter J. Mogayzel is also published. He has 74 publications published. The lastest publication: "Sleep-disordered breathing in children with achondroplasia.'
Publications
- ESCF Care Guidelines beyond Europe.
- Rationale and design of a randomized trial of home electronic symptom and lung function monitoring to detect Cystic fibrosis pulmonary exacerbations: The early interve...
- Environmental allergies and respiratory morbidities in Cystic fibrosis.
- A pilot study to examine the effect of chronic treatment with immunosuppressive drugs on mucociliary clearance in a vagotomized murine model.
- Pain is a common problem affecting clinical outcomes in adults with Cystic fibrosis.
- Exercise improves lung function and habitual activity in children with Cystic fibrosis.
- Update in Cystic fibrosis 2010.
- Implementation of the first worldwide quality assurance program for Cystic fibrosis multiple mutation detection in population-based screening.
- Treatment of Plastic Bronchitis by Orthotopic Heart Transplantation.
- Longitudinal association between medication adherence and lung health in people with Cystic fibrosis.
- Multicenter evaluation of infant lung function tests as Cystic fibrosis clinical trial endpoints.
- Location and duration of treatment of Cystic fibrosis respiratory exacerbations do not affect outcomes.
- False negative Cystic fibrosis newborn screen.
- Update in Cystic fibrosis 2009.
- 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.
- Cytomegalovirus immunoglobulin decreases the risk of cytomegalovirus infection but not disease after pediatric lung transplantation.
- The risk, prevention, and outcome of cytomegalovirus after pediatric lung transplantation.
- Accuracy of tobramycin levels obtained from central venous access devices in patients with Cystic fibrosis is technique dependent.
- Increased mortality after pulmonary fungal infection within the first year after pediatric lung transplantation.
- Spontaneous resolution of diffuse persistent pulmonary interstitial emphysema.
- Dietary supplement use in pediatric patients with Cystic fibrosis.
- Pulmonary dysfunction in pediatric hematopoietic stem cell transplant patients: non-infectious and long-term complications.
- Pulmonary dysfunction in pediatric hematopoietic stem cell transplant patients: overview, diagnostic considerations, and infectious complications.
- Albuterol improves impaired mucociliary clearance after lung transplantation.
- De novo biosynthetic profiling of high abundance proteins in Cystic fibrosis lung epithelial cells.
- Pharmacoproteomics of 4-phenylbutyrate-treated IB3-1 Cystic fibrosis bronchial epithelial cells.
- Modulation of Sp1 and Sp3 in lung epithelial cells regulates ClC-2 chloride channel expression.
- Extracorporeal photopheresis in the treatment of persistent rejection in a pediatric lung transplant recipient.
- Effect of adeno-associated virus-specific immunoglobulin G in human amniotic fluid on gene transfer.
- Bilateral cadaveric lobar transplantation from a marginal adult donor to a pediatric recipient.
- Bilateral diaphragm paralysis following lung transplantation and cardiac surgery in a 17-year-old.
- Effect of the reducing environment on the accumulation of elastin and collagen in cultured smooth-muscle cells.
- Glycosaminoglycan content in neonatal rat aortic smooth muscle cell cultures.
- Congo red binding of elastin in aortic smooth muscle cell cultures.
- Elastase effect on the extracellular matrix of rat aortic smooth muscle cells in culture.
- A micromethod for the purification of lysyl oxidase.
- Mammalian cell growth on collagen-hydrogels.
- Effect of protein-hydroxyethylmethacrylate hydrogels on cultured endothelial cells.
- Rapid quantitation of desmosine content in tissue hydrolysates by high-performance liquid chromatography.
- Functional human CFTR produced by stable Chinese hamster ovary cell lines derived using yeast artificial chromosomes.
- Sleep-disordered breathing in children with achondroplasia.
- CFTR intron 1 increases luciferase expression driven by CFTR 5'-flanking DNA in a yeast artificial chromosome.
- An unusual case of fatal pulmonary allograft rejection.
- Eosinophilic infiltrates in a pulmonary allograft: a case and review of the literature.
- Variability in immunization guidelines in children before and after lung transplantation.
- American Society of Transplantation executive summary on pediatric lung transplantation.
- Minimal acute rejection in pediatric lung transplantation--does it matter?
- Familial neuroendocrine cell hyperplasia of infancy.
- Transient effectiveness of vitamin D2 therapy in pediatric Cystic fibrosis patients.
- Acute inhalation of hypertonic saline does not improve mucociliary clearance in all children with Cystic fibrosis.
- Lung function and late pulmonary complications among survivors of hematopoietic stem cell transplantation during childhood.
- Cystic fibrosis pulmonary guidelines: pulmonary complications: hemoptysis and pneumothorax.
- Early eradication of Pseudomonas aeruginosa in patients with Cystic fibrosis.
- CFTR transcription defects in pancreatic sufficient Cystic fibrosis patients with only one mutation in the coding region of CFTR.
- [Use of flexible fiberoptic bronchoscopy in pediatric clinical practice].
- Vagal control of mucociliary clearance in murine lungs: a study in a chronic preparation.
- Cystic fibrosis pulmonary guidelines: treatment of pulmonary exacerbations.
- Respiratory viral infections within one year after pediatric lung transplant.
- A previously healthy adolescent with evolving infiltrates and progressive respiratory distress.
- Skeletal dysplasias and their effect on the respiratory system.
- Variants in mannose-binding lectin and tumour necrosis factor alpha affect survival in Cystic fibrosis.
- Current treatment recommendations for correcting vitamin D deficiency in pediatric patients with Cystic fibrosis are inadequate.
- Chronic inhalation of nebulized levalbuterol does not increase mucociliary clearance in healthy subjects.
- Diagnostic sweat testing: the Cystic Fibrosis Foundation guidelines.
- Cystic fibrosis pulmonary guidelines: chronic medications for maintenance of lung health.
- Membrane-associated heparan sulfate is not required for rAAV-2 infection of human respiratory epithelia.
- cis-Acting elements within CFTR 5''-flanking DNA are not sufficient to decrease gene expression in response to phorbol ester.
- Cyclosporin and tacrolimus do not potentiate oxidative damage in pulmonary epithelial cells.
- Variability in standard care for cytomegalovirus prevention and detection in pediatric lung transplantation: survey of eight pediatric lung transplant programs.
- Ciprofloxacin-induced renal insufficiency in Cystic fibrosis.
- Role of tropoelastin fragmentation in elastogenesis in rat smooth muscle cells.
- A comparison of cultured aortic smooth muscle cells from different sources: are they all the same?
Schools
Boston University School Of Medicine
University Of Washington Med Center
University of Washington
Johns Hopkins Hospital
Conditions Treated
- Asthma
- Bronchiolitis
- Cystic Fibrosis
Doctors Specialties
- Pediatric Critical Care Medicine
- Pediatric Pulmonology
Accepted Insurances
Awards
- Fellow (FAAP)
- Fellow (FACP)
Education
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University of Washington -
Boston University School of Medicine
Hospital
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Anne Arundel Medical Center -
Johns Hopkins Hospital
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