Daigle K - Search Results

1

The BIT:S (Bronchopulmonary Dysplasia Interdisciplinary Team: Severe) Initiative at Women and Infants Hospital of Rhode Island.

McKinney RL, Shukla K, Daigle K, Zeigler J, Muller M, Keszler M. McKinney RL, et al. Among authors: daigle k. R I Med J (2013). 2019 Apr 1;102(3):22-25. R I Med J (2013). 2019. PMID: 30943667

2

Office management of bronchopulmonary dysplasia.

Daigle KL, Cloutier MM. Daigle KL, et al. Compr Ther. 1997 Oct;23(10):656-62. Compr Ther. 1997. PMID: 9327181 Review. No abstract available.

3

Pulmonary function abnormalities in Prader-Willi syndrome.

Hákonarson H, Moskovitz J, Daigle KL, Cassidy SB, Cloutier MM. Hákonarson H, et al. Among authors: daigle kl. J Pediatr. 1995 Apr;126(4):565-70. doi: 10.1016/s0022-3476(95)70350-0. J Pediatr. 1995. PMID: 7699534

4

The influence of pulmonary function testing on the management of asthma in children.

Nair SJ, Daigle KL, DeCuir P, Lapin CD, Schramm CM. Nair SJ, et al. J Pediatr. 2005 Dec;147(6):797-801. doi: 10.1016/j.jpeds.2005.07.023. J Pediatr. 2005. PMID: 16356434 Clinical Trial.

5

Diuretics for very low birth weight infants in the first 28 days: a survey of the U.S. neonatologists.

Hagadorn JI, Sanders MR, Staves C, Herson VC, Daigle K. Hagadorn JI, et al. Among authors: daigle k. J Perinatol. 2011 Oct;31(10):677-81. doi: 10.1038/jp.2011.11. Epub 2011 Mar 10. J Perinatol. 2011. PMID: 21394079

6

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.

7

Socioeconomic status and the likelihood of antibiotic treatment for signs and symptoms of pulmonary exacerbation in children with cystic fibrosis.

Schechter MS, McColley SA, Regelmann W, Millar SJ, Pasta DJ, Wagener JS, Konstan MW, Morgan WJ; Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis. Schechter MS, et al. J Pediatr. 2011 Nov;159(5):819-824.e1. doi: 10.1016/j.jpeds.2011.05.005. Epub 2011 Jun 25. J Pediatr. 2011. PMID: 21705017 Free PMC article.

8

Risk factors for age at initial Pseudomonas acquisition in the cystic fibrosis epic observational cohort.

Rosenfeld M, Emerson J, McNamara S, Thompson V, Ramsey BW, Morgan W, Gibson RL; EPIC Study Group. Rosenfeld M, et al. J Cyst Fibros. 2012 Sep;11(5):446-53. doi: 10.1016/j.jcf.2012.04.003. Epub 2012 May 1. J Cyst Fibros. 2012. PMID: 22554417 Free PMC article. Clinical Trial.

9

Risk factors for lung function decline in a large cohort of young cystic fibrosis patients.

Cogen J, Emerson J, Sanders DB, Ren C, Schechter MS, Gibson RL, Morgan W, Rosenfeld M; EPIC Study Group. Cogen J, et al. Pediatr Pulmonol. 2015 Aug;50(8):763-70. doi: 10.1002/ppul.23217. Epub 2015 Jun 9. Pediatr Pulmonol. 2015. PMID: 26061914 Free PMC article.

10

Probability of treatment following acute decline in lung function in children with cystic fibrosis is related to baseline pulmonary function.

Morgan WJ, Wagener JS, Yegin A, Pasta DJ, Millar SJ, Konstan MW; Scientific Advisory Group, investigators; coordinators of the Epidemiologic Study of Cystic Fibrosis. Morgan WJ, et al. J Pediatr. 2013 Oct;163(4):1152-7.e2. doi: 10.1016/j.jpeds.2013.05.013. Epub 2013 Jun 27. J Pediatr. 2013. PMID: 23810128 Free PMC article.

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