McCoy K - Search Results

1

Impact of Elexacaftor-Tezacaftor-Ivacaftor on lung disease in cystic fibrosis.

Gushue C, Eisner M, Bai S, Johnson T, Holtzlander M, McCoy K, Sheikh S. Gushue C, et al. Among authors: mccoy k. Pediatr Pulmonol. 2023 Aug;58(8):2308-2316. doi: 10.1002/ppul.26485. Epub 2023 May 24. Pediatr Pulmonol. 2023. PMID: 37222417

2

Presentation of bronchial mucoepidermoid carcinoma as unilateral hyperlucent lung.

Allen ED, McCoy KS. Allen ED, et al. Among authors: mccoy ks. Pediatr Pulmonol. 1990;8(4):294-7. doi: 10.1002/ppul.1950080415. Pediatr Pulmonol. 1990. PMID: 2371078 No abstract available.

3

Adult-type pulmonary function tests in infants without respiratory disease.

Castile R, Filbrun D, Flucke R, Franklin W, McCoy K. Castile R, et al. Among authors: mccoy k. Pediatr Pulmonol. 2000 Sep;30(3):215-27. doi: 10.1002/1099-0496(200009)30:3<215::aid-ppul6>3.0.co;2-v. Pediatr Pulmonol. 2000. PMID: 10973040 Clinical Trial.

4

Compression of the trachea by the innominate artery in a 2-month-old child.

Shell R, Allen E, Mutabagani K, Long F, Davis JT, McCoy K, Castile R. Shell R, et al. Among authors: mccoy k. Pediatr Pulmonol. 2001 Jan;31(1):80-5. doi: 10.1002/1099-0496(200101)31:1<80::aid-ppul1011>3.0.co;2-o. Pediatr Pulmonol. 2001. PMID: 11180679

5

Urinary leukotriene E(4) excretion during the first month of life and subsequent bronchopulmonary dysplasia in premature infants.

Sheikh S, Null D, Gentile D, Bimle C, Skoner D, McCoy K, Guthrie R. Sheikh S, et al. Among authors: mccoy k. Chest. 2001 Jun;119(6):1749-54. doi: 10.1378/chest.119.6.1749. Chest. 2001. PMID: 11399701 Clinical Trial.

6

Chronic aspiration without gastroesophageal reflux as a cause of chronic respiratory symptoms in neurologically normal infants.

Sheikh S, Allen E, Shell R, Hruschak J, Iram D, Castile R, McCoy K. Sheikh S, et al. Among authors: mccoy k. Chest. 2001 Oct;120(4):1190-5. doi: 10.1378/chest.120.4.1190. Chest. 2001. PMID: 11591559

7

Gas trapping in normal infants and in infants with cystic fibrosis.

Castile RG, Iram D, McCoy KS. Castile RG, et al. Pediatr Pulmonol. 2004 May;37(5):461-9. doi: 10.1002/ppul.10446. Pediatr Pulmonol. 2004. PMID: 15095331

8

The role of computerized order sets in pediatric inpatient asthma treatment.

Chisolm DJ, McAlearney AS, Veneris S, Fisher D, Holtzlander M, McCoy KS. Chisolm DJ, et al. Pediatr Allergy Immunol. 2006 May;17(3):199-206. doi: 10.1111/j.1399-3038.2005.00362.x. Pediatr Allergy Immunol. 2006. PMID: 16672007

9

Barriers to adherence to cystic fibrosis infection control guidelines.

Garber E, Desai M, Zhou J, Alba L, Angst D, Cabana M, Saiman L; CF Infection Control Study Consortium. Garber E, et al. Pediatr Pulmonol. 2008 Sep;43(9):900-7. doi: 10.1002/ppul.20876. Pediatr Pulmonol. 2008. PMID: 18671274

10

Initial Pseudomonas aeruginosa treatment failure is associated with exacerbations in cystic fibrosis.

Mayer-Hamblett N, Kronmal RA, Gibson RL, Rosenfeld M, Retsch-Bogart G, Treggiari MM, Burns JL, Khan U, Ramsey BW; EPIC Investigators. Mayer-Hamblett N, et al. Pediatr Pulmonol. 2012 Feb;47(2):125-34. doi: 10.1002/ppul.21525. Epub 2011 Aug 9. Pediatr Pulmonol. 2012. PMID: 21830317 Free PMC article. Clinical Trial.

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