University of Minnesota Amplatz Children’s Hospital Position(s)
Pediatric Pulmonologist

Other Related Positions Currently Held
Associate Professor, Divisons of Pediatric Pulmonary and Critical Care Medicine and Pediatric Infectious Diseases, Department of Pediatrics, University of Minnesota

Specialties
Cystic Fibrosis
Pulmonology

Board Certifications
General Pediatrics
Pediatric Pulmonology
Pediatric Infectious Disease

Sees Patients At
University of Minnesota Amplatz Children’s Hospital (Cystic Fibrosis, Infectious Diseases, Pulmonology, Organ Transplant)
Pediatric Specialty Clinic (Minneapolis)
The Minnesota Cystic Fibrosis Center (Minneapolis)
Specialty Clinic for Children (Burnsville)

Clinical Interests
Asthma
Bronchiectasis
Bronchiolitis
Chest Pain
Chronic Obstructive Pulmonary Disease (COPD)
Congenital Malformation of the Chest and Lungs
Cystic Fibrosis
Emphysema
Hemoptysis
Pleurisy
Pneumonia
Pulmonary Dysplasia
Pulmonary Embolism
Recurrent and Persistent Cough
SARS
Smoking Cessation
Tuberculosis

Education
Medical School
State University of New York, Downstate Medical Center, Brooklyn, N. Y.

Site of Residency
University of Minnesota (Pediatrics)

Site of Fellowship
University of Minnesota (Infectious Disease)

Awards and Honors
Best Doctors in America®, 2009-2010
Mpls. St. Paul Magazine Top Doctors 2009
Best Doctors in America®, 2007-2008

Selected Recent Publications
Regelmann, W.E., Siefferman, C.M., Herron, J.M., Elliott, G.R., Clawson, C.C., and Gray, B.H. 1995. Sputum peroxidase activity correlates with the severity of lung disease in cystic fibrosis. Pediatr Pulmonol 19:1-9.

Brottman, G.M., Regelmann, W.E., Slungaard, A., and Wangensteen, O.D. 1996. Effect of eosinophil peroxidase on airway epithelial permeability in the guinea pig. Pediatr Pulmonol 21:159-166.

Milla, C., Doherty, L., Raatz, S., Schwarzenberg, S.J., Regelmann, W., and Moran, A. 1996. Glycemic response to dietary supplements in cystic fibrosis is dependent on the carbohydrate content of the formula. JPEN J Parenter Enteral Nutr 20:182-186.

Milla, C.E., Wielinski, C.L., and Regelmann, W.E. 1996. Clinical significance of the recovery of Aspergillus species from the respiratory secretions of cystic fibrosis patients. Pediatr Pulmonol 21:6-10.

Wilmott, R.W., Amin, R.S., Colin, A.A., DeVault, A., Dozor, A.J., Eigen, H., Johnson, C., Lester, L.A., McCoy, K., McKean, L.P., et al. 1996. Aerosolized recombinant human DNase in hospitalized cystic fibrosis patients with acute pulmonary exacerbations. Am J Respir Crit Care Med 153:1914-1917.

Regelmann, W.E., Schneider, L.A., Fahrenkrug, S.C., Gray, B.H., Johnson, S., Herron, J.M., Clawson, C.C., Clawson, D.J., and Wangensteen, O.D. 1997. Proteinase-free myeloperoxidase increases airway epithelial permeability in a whole trachea model. Pediatr Pulmonol 24:29-34.

Shreve, M.R., Johnson, S.J., Milla, C.E., Wielinski, C.L., and Regelmann, W.E. 1997. PCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacia infection. Am J Respir Crit Care Med 155:984-989.

Morgan, W.J., Butler, S.M., Johnson, C.A., Colin, A.A., FitzSimmons, S.C., Geller, D.E., Konstan, M.W., Light, M.J., Rabin, H.R., Regelmann, W.E., et al. 1999. Epidemiologic study of cystic fibrosis: design and implementation of a prospective, multicenter, observational study of patients with cystic fibrosis in the U.S. and Canada. Pediatr Pulmonol 28:231-241.

Shreve, M.R., Butler, S., Kaplowitz, H.J., Rabin, H.R., Stokes, D., Light, M., and Regelmann, W.E. 1999. Impact of microbiology practice on cumulative prevalence of respiratory tract bacteria in patients with cystic fibrosis. J Clin Microbiol 37:753-757.

McCarty, N.A., Standaert, T.A., Teresi, M., Tuthill, C., Launspach, J., Kelley, T.J., Milgram, L.J., Hilliard, K.A., Regelmann, W.E., Weatherly, M.R., et al. 2002. A phase I randomized, multicenter trial of CPX in adult subjects with mild cystic fibrosis. Pediatr Pulmonol 33:90-98.

Garner, H.P., Phillips, J.R., Herron, J.G., Severson, S.J., Milla, C.E., and Regelmann, W.E. 2004. Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis. J Lab Clin Med 144:127-133.

Rabin, H.R., Butler, S.M., Wohl, M.E., Geller, D.E., Colin, A.A., Schidlow, D.V., Johnson, C.A., Konstan, M.W., and Regelmann, W.E. 2004. Pulmonary exacerbations in cystic fibrosis. Pediatr Pulmonol 37:400-406.