Dean and VP of Health Affairs, Univerity of Cincinnati College of Medicine
Pediatric Pulmonology
Dr. Thomas F. Boat, MD
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Thomas F. Boat, MD works in the field of Pediatric Pulmonology. He studied medicine at University of Iowa Carver College of Medicine. University of Iowa Carver College of Medicine is ranked 29/16 in Research/PrimaryCare. He received 2 awards: "Elected Member" and "Whos Who in Medicine and Healthcare". Thomas Boat is also published. He has 100 publications published. The lastest publication: "Human respiratory tract secretion. Mucous glycoproteins of nonpurulent tracheobronchial secretions, and sputum of patients with bronchitis and cystic fibrosis.'
Publications
- Children With Mental Disorders Who Receive Disability Benefits: A Report From the IOM.
- Stemming Early Progression of Airways Disease in Cystic Fibrosis.
- IOM Review of FDA--approved biologics labeled or studied for pediatric use.
- Insights from trends in biomedical research funding.
- Implications of parental bereavement and other family adversities for preventive and health promotion pediatric services.
- From waste to value in health care.
- The future of pediatric research.
- Promoting translational research in academic health centers: navigating the "roadmap".
- Pediatric faculty members' attitudes about part-time faculty positions and policies to support part-time faculty: a study at one medical center.
- Pediatric Subspecialty Training Fellowships at Cincinnati Children's Hospital Medical Center (CCHMC).
- Pseudomonas aeruginosa endogenous endophthalmitis with choroidal abscess in a patient with cystic fibrosis.
- Listening to families: first steps toward improved hospital care.
- Improving health outcomes for children.
- Opportunity and response.
- Evolution of subspecialty care in pediatrics.
- Proteoglycan secretory components of surface epithelial cells in postnatal ferret trachea.
- Final report of the FOPE II Financing of Pediatric Education Workgroup.
- Federation of Pediatric Organizations Task Force on Women in Pediatrics: considerations for part-time training and employment for research-intensive fellows and faculty.
- Care of high-risk infants.
- Sulfate concentrations and transport in human bronchial epithelial cells.
- Increased adherence of Staphylococcus aureus from cystic fibrosis lungs to airway epithelial cells.
- Outcome measures for clinical trials in cystic fibrosis. Summary of a Cystic Fibrosis Foundation consensus conference.
- Pseudomembranous colitis in a patient with cystic fibrosis.
- Differential effects of ozone on lung epithelial lining fluid volume and protein content.
- Alteration of sulfation of glycoconjugates, but not sulfate transport and intracellular inorganic sulfate content in cystic fibrosis airway epithelial cells.
- Biochemistry of airway mucus secretions.
- Heart failure in cystic fibrosis. Treatment and prognosis of cor pulmonale with failure of the right side of the heart.
- Quantitation of radiolabeled mucous glycoproteins secreted by tracheal explants.
- Psychosocial functioning of children with cystic fibrosis.
- Treatment and prognosis of nasal polyps in cystic fibrosis.
- Mucin release from rabbit tracheal epithelium in response to sera from normal and cystic fibrosis subjects.
- A comparative study of lysozyme and its secretion by tracheal epithelium.
- Identification of a major heparin-precipitable protein in human serum and its relationship to cystic fibrosis.
- Treatment and prognosis of rectal prolapse in cystic fibrosis.
- Solution properties of porcine submaxillary mucin.
- Mucous glycoproteins from cat tracheal goblet cells and mucous glands separated with EDTA.
- EDTA-mediated separation of cat tracheal lining epithelium.
- Are measurements of urine enzymes useful during aminoglycoside therapy?
- The obesity hypoventilation syndrome in children with the Prader-Willi syndrome: a possible role for familial decreased response to carbon dioxide.
- The carbohydrate content of IgG from patients with cystic fibrosis.
- Surface architecture of the mucosal epithelium of the cat trachea: II. Structure and dynamics of the membranous portion.
- Surface architecture of the mucosal epithelium of the cat trachea: I. Cartilaginous portion.
- Proteinases of Pseudomonas aeruginosa evoke mucin release by tracheal epithelium.
- Stridor due to radiotransparent esophageal foreign body.
- Time course of hemosiderin production and clearance by human pulmonary macrophages.
- Proteinases release mucin from airways goblet cells.
- Beta adrenergic receptors in lymphocytes and granulocytes from patients with cystic fibrosis.
- Carcinoma of extrahepatic biliary system in an adult with cystic fibrosis.
- Concentrations of alpha 1-proteinase inhibitor and alpha 2-macroglobulin in serum and lung secretions of intubated infants.
- Beta-adrenergic modulation of mucin secretion in cat trachea.
- Neurohormonal receptors and cyclic AMP-binding proteins in rabbit tracheal mucosa-submucosa.
- Obstructive azoospermia as a diagnostic criterion for the cystic fibrosis syndrome.
- The alpha 2-adrenergic system of the platelet in cystic fibrosis.
- Effects of alpha-tocopherol on platelet membrane function in cystic fibrosis.
- Pneumothorax in cystic fibrosis.
- Sodium concentration in unstimulated parotid saliva and on oral mucosa in normal subjects and in patients with cystic fibrosis.
- Mucus, calcium, sweat, water, and permeability in cystic fibrosis.
- Serum alkaline phosphatase in cystic fibrosis. Interpretation of elevated values based on electrophoretic isoenzyme analyses.
- Toxic effects of oxygen on cultured human neonatal respiratory epithelium.
- Cystic fibrosis care-further considerations.
- Purification and properties of the calcium-precipitable protein in submaxillary saliva of normal and cystic fibrosis subjects.
- Standardized assay for the sodium reabsorption inhibitory effect and studies of its salivary gland distribution in patients with cystic fibrosis.
- Human respiratory tract secretions. 1. Mucous glycoproteins secreted by cultured nasal polyp epithelium from subjects with allergic rhinitis and with cystic fibrosis.
- Studies of particulate iodoproteins in the rat thyroid.
- Flow-rates and electrolytes in minor-salivary-gland saliva in normal subjects and patients with cystic fibrosis.
- Altered urinary excretion of elastin cross-links in premature infants who develop bronchopulmonary dysplasia.
- Immune complexes and complement abnormalities in patients with cystic fibrosis. Increased mortality associated with circulating immune complexes and decreased function...
- Features of developing ferret tracheal epithelium: ultrastructural observations of in vivo and in vitro differentiation of ciliated cells.
- Developmental changes in glycoconjugate secretion by ferret tracheas.
- Cystic fibrosis: overview.
- Development, organization, and function of tight junctional complexes in the tracheal epithelium of infant ferrets.
- Increased sulfation of glycoconjugates by cultured nasal epithelial cells from patients with cystic fibrosis.
- Epithelial cell dysfunction in cystic fibrosis: implications for airways disease.
- Developmental changes of ferret tracheal mucin composition and biosynthesis.
- Postnatal development of tracheal surface epithelium and submucosal glands in the ferret.
- Ciliary dysmorphology and dysfunction--primary or acquired?
- Lithium, clinical research, and cystic fibrosis.
- Cystic fibrosis: a current review.
- Loss of cilia and altered phenotypic expression of ciliated cells after acute sulfur dioxide exposure.
- Development of mucociliary transport in the postnatal ferret trachea.
- Hyperreactivity to cow milk in young children with pulmonary hemosiderosis and cor pulmonale secondary to nasopharyngeal obstruction.
- Open thoracotomy for pneumothorax in cystic fibrosis.
- Human respiratory tract secretions. 2. Effect of cholinergic and adrenergic agents on in vitro release of protein and mucous glycoprotein.
- Symptomatic hepatic disease in cystic fibrosis: incidence, course, and outcome of portal systemic hunting.
- Tracheobronchial mucus secretion in vivo and in vitro by epithelial tissues from cystic fibrosis and control subjects.
- Human respiratory tract secretion. Mucous glycoproteins of nonpurulent tracheobronchial secretions, and sputum of patients with bronchitis and cystic fibrosis.
- Course of cystic fibrosis in black patients.
- Course of cystic fibrosis in 95 patients.
- Human tracheobronchial secretions: development of mucous glycoprotein and lysozyme-secreting systems.
- The effect of early diagnosis and treatment in cystic fibrosis: a seven-year study of 16 sibling pairs.
- Cystic fibrosis diagnosed after age 13. Twenty-five teenage and adult patients including three asymptomatic men.
- Immunologic studies in cow''s milk-induced pulmonary hemosiderosis.
- Chronic bronchitis and cystic fibrosis: two chronic obstructive lung diseases of adults.
- Progesterone treatment of the obesity hypoventilation syndrome in a child.
- Treatment and prognosis of lobar and segmental atelectasis in cystic fibrosis.
- Echocardiographic changes in children with pulmonary hypertension secondary to upper airway obstruction.
- Cystic fibrosis: the prognosis for five-year survival.
- Treatment and prognosis of massive hemoptysis in cystic fibrosis.
- Intermediate-range sweat chloride concentration and Pseudomonas bronchitis. A cystic fibrosis variant with preservation of exocrine pancreatic function.
Schools
University of Ia Roy J amp L Carver Com
Minn Hosps
Case West Res
Doctors Specialties
- Pediatric Pulmonology
Accepted Insurances
Awards
- Elected Member
- Whos Who in Medicine and Healthcare
Education
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University of Minnesota at Fairview -
University of Iowa Carver College of Medicine
Hospital
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Cincinnati Children's Hospital Medical Center
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