Associate Professor, Pediatrics, University of Pittsburgh School of Medicine

Pediatric Pulmonology

Daniel J. Weiner, MD works in the field of Pediatric Pulmonology. He went to medical school at University of Michigan Medical School. Daniel J. Weiner is also published. He has 40 publications published. The lastest publication: "The innate immune system in cystic fibrosis lung disease.'

Publications

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• Cystic fibrosis program directors' attitudes toward sexual and reproductive health in young women with CF.
• Dexmedetomidine for infant Pulmonary function testing.
• Lung function over the first 3 years of life in children with congenital diaphragmatic hernia.
• Overweight and obesity in patients with Cystic fibrosis: A center-based analysis.
• Respiratory muscle function in infants with spinal muscular atrophy type I.
• Changes in gastric pressure and volume during mechanical in-exsufflation.
• Elevated sweat chloride concentration in children without Cystic fibrosis who are receiving topiramate therapy.
• Resonant frequency does not predict high-frequency chest compression settings that maximize airflow or volume.
• Re: Lum S, Hoo AF, Hulskamp G, Wade A, Stocks J. Potential Misinterpretation of Infant Lung Function Unless Prospective Healthy Controls Are Studied. Pediatr Pulmonol ...
• Late presentation of congenital diaphragmatic hernia in patients with Cystic fibrosis.
• Pre-transplant Lung function is predictive of survival following pediatric bone marrow transplantation.
• Lung function, pulmonary complications, and mortality after allogeneic blood and marrow transplantation in children.
• Heated, humidified high-flow nasal cannula therapy.
• The p38 mitogen-activated protein kinase signaling pathway is coupled to Toll-like receptor 5 to mediate gene regulation in response to Pseudomonas aeruginosa infectio...
• Asthma as a barrier to children's physical activity.
• Pulmonary function abnormalities in children treated with whole Lung irradiation.
• Human airway epithelial cells sense Pseudomonas aeruginosa infection via recognition of flagellin by Toll-like receptor 5.
• Antibacterial activities of rhodamine B-conjugated gelsolin-derived peptides compared to those of the antimicrobial peptides cathelicidin LL37, magainin II, and melittin.
• Erythropoietin gene therapy leads to autoimmune anemia in macaques.
• Use of the mechanical in-exsufflator in pediatric patients with neuromuscular disease and impaired cough.
• Noninvasive measurement of the tension-time index in children with neuromuscular disease.
• Airway epithelia regulate expression of human beta-defensin 2 through Toll-like receptor 2.
• The antimicrobial activity of the cathelicidin LL37 is inhibited by F-actin bundles and restored by gelsolin.
• Human fetal trachea-SCID mouse xenografts: efficacy of vesicular stomatitis virus-G pseudotyped lentiviral-mediated gene transfer.
• Infant Pulmonary function testing.
• Development of novel antibacterial peptides that kill resistant isolates.
• beta-Defensin 1 contributes to Pulmonary innate immunity in mice.
• Respiratory tract infections in Cystic fibrosis.
• Toll-like receptor 4 mediates innate immune responses to Haemophilus influenzae infection in mouse Lung.
• Tracheal schwannoma presenting as status Asthmaticus in a sixteen-year-old boy: airway considerations and removal with the CO2 laser.
• Rhesus monkey (Macaca mulatta) mucosal antimicrobial peptides are close homologues of human molecules.
• Transduction of well-differentiated airway epithelium by recombinant adeno-associated virus is limited by vector entry.
• The innate immune system in cystic fibrosis Lung disease.
• Transfer of a cathelicidin peptide antibiotic gene restores bacterial killing in a Cystic fibrosis xenograft model.
• Filovirus-pseudotyped lentiviral vector can efficiently and stably transduce airway epithelia in vivo.
• Salt-independent abnormality of antimicrobial activity in Cystic fibrosis airway surface fluid.
• Augmentation of innate host defense by expression of a cathelicidin antimicrobial peptide.
• Mouse beta-defensin 3 is an inducible antimicrobial peptide expressed in the epithelia of multiple organs.
• Pseudomonas infection and mucociliary and absorptive clearance in the cystic fibrosis Lung.

Schools

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• University of Mi Med Sch

• St Christophers Hospital Chldn

• Thos Jefferson University Hospital

• University Of Mi Hosps and Health Ctrs

Conditions Treated

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• Asthma
• Bronchitis
• BronchoPulmonary Dysplasia
• Collapsed Lung (Pneumothorax)
• View All

Doctors Specialties

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• Pediatric Pulmonology

Accepted Insurances

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Education

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• Thomas Jefferson University
• University of Michigan Hospitals and Health Centers
• University of Michigan Medical School

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