Regelmann WE - Search Results

1

Longitudinal assessment of lung function from infancy to childhood in patients with cystic fibrosis.

Harrison AN, Regelmann WE, Zirbes JM, Milla CE. Harrison AN, et al. Among authors: regelmann we. Pediatr Pulmonol. 2009 Apr;44(4):330-9. doi: 10.1002/ppul.20994. Pediatr Pulmonol. 2009. PMID: 19274621

2

Clinical significance of the recovery of Aspergillus species from the respiratory secretions of cystic fibrosis patients.

Milla CE, Wielinski CL, Regelmann WE. Milla CE, et al. Among authors: regelmann we. Pediatr Pulmonol. 1996 Jan;21(1):6-10. doi: 10.1002/(SICI)1099-0496(199601)21:1<6::AID-PPUL1>3.0.CO;2-R. Pediatr Pulmonol. 1996. PMID: 8776259

3

Peroxidase activity within circulating neutrophils correlates with pulmonary phenotype in cystic fibrosis.

Garner HP, Phillips JR, Herron JG, Severson SJ, Milla CE, Regelmann WE. Garner HP, et al. Among authors: regelmann we. J Lab Clin Med. 2004 Sep;144(3):127-33. doi: 10.1016/j.lab.2004.04.010. J Lab Clin Med. 2004. PMID: 15454881

4

Risk factors for onset of persistent respiratory symptoms in children with cystic fibrosis.

McColley SA, Ren CL, Schechter MS, Regelmann WE, Pasta DJ, Konstan MW; Epidemiologic Study of Cystic Fibrosis. McColley SA, et al. Among authors: regelmann we. Pediatr Pulmonol. 2012 Oct;47(10):966-72. doi: 10.1002/ppul.22519. Epub 2012 Feb 22. Pediatr Pulmonol. 2012. PMID: 22359344 Free PMC article.

5

The impact of incident methicillin resistant Staphylococcus aureus detection on pulmonary function in cystic fibrosis.

Sawicki GS, Rasouliyan L, Pasta DJ, Regelmann WE, Wagener JS, Waltz DA, Ren CL. Sawicki GS, et al. Among authors: regelmann we. Pediatr Pulmonol. 2008 Nov;43(11):1117-1123. doi: 10.1002/ppul.20914. Pediatr Pulmonol. 2008. PMID: 18846559

6

PCR ribotyping and endonuclease subtyping in the epidemiology of Burkholderia cepacia infection.

Shreve MR, Johnson SJ, Milla CE, Wielinski CL, Regelmann WE. Shreve MR, et al. Among authors: regelmann we. Am J Respir Crit Care Med. 1997 Mar;155(3):984-9. doi: 10.1164/ajrccm.155.3.9117036. Am J Respir Crit Care Med. 1997. PMID: 9117036

7

Comparison of quantitative sweat chloride methods after positive newborn screen for cystic fibrosis.

Laguna TA, Lin N, Wang Q, Holme B, McNamara J, Regelmann WE. Laguna TA, et al. Among authors: regelmann we. Pediatr Pulmonol. 2012 Aug;47(8):736-42. doi: 10.1002/ppul.21608. Epub 2012 Jan 3. Pediatr Pulmonol. 2012. PMID: 22786625 Free PMC article.

8

Standard care versus protocol based therapy for new onset Pseudomonas aeruginosa in cystic fibrosis.

Mayer-Hamblett N, Rosenfeld M, Treggiari MM, Konstan MW, Retsch-Bogart G, Morgan W, Wagener J, Gibson RL, Khan U, Emerson J, Thompson V, Elkin EP, Ramsey BW; EPIC; ESCF Investigators. Mayer-Hamblett N, et al. Pediatr Pulmonol. 2013 Oct;48(10):943-53. doi: 10.1002/ppul.22693. Epub 2013 Jul 2. Pediatr Pulmonol. 2013. PMID: 23818295 Free PMC article. Clinical Trial.

9

Presence of methicillin resistant Staphylococcus aureus in respiratory cultures from cystic fibrosis patients is associated with lower lung function.

Ren CL, Morgan WJ, Konstan MW, Schechter MS, Wagener JS, Fisher KA, Regelmann WE; Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Ren CL, et al. Among authors: regelmann we. Pediatr Pulmonol. 2007 Jun;42(6):513-8. doi: 10.1002/ppul.20604. Pediatr Pulmonol. 2007. PMID: 17469151

10

Glycemic response to dietary supplements in cystic fibrosis is dependent on the carbohydrate content of the formula.

Milla C, Doherty L, Raatz S, Schwarzenberg SJ, Regelmann W, Moran A. Milla C, et al. JPEN J Parenter Enteral Nutr. 1996 May-Jun;20(3):182-6. doi: 10.1177/0148607196020003182. JPEN J Parenter Enteral Nutr. 1996. PMID: 8776690 Clinical Trial.

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