Doershuk CF - Search Results

1

Pseudomonas aeruginosa isolates: comparisons of isolates from campers and from sibling pairs with cystic fibrosis.

Thomassen MJ, Demko CA, Doershuk CF, Root JM. Thomassen MJ, et al. Among authors: doershuk cf. Pediatr Pulmonol. 1985 Jan-Feb;1(1):40-5. doi: 10.1002/ppul.1950010110. Pediatr Pulmonol. 1985. PMID: 3932947

2

Monocytes in cystic fibrosis: responsiveness to microbial stimuli.

Thomassen MJ, Barna BP, Farmer MO, Doershuk CF, Stern RC. Thomassen MJ, et al. Among authors: doershuk cf. Pediatr Pulmonol. 1990;8(3):178-81. doi: 10.1002/ppul.1950080309. Pediatr Pulmonol. 1990. PMID: 2161509

3

Cystic fibrosis: a review of pulmonary infections and interventions.

Thomassen MJ, Demko CA, Doershuk CF. Thomassen MJ, et al. Among authors: doershuk cf. Pediatr Pulmonol. 1987 Sep-Oct;3(5):334-51. doi: 10.1002/ppul.1950030510. Pediatr Pulmonol. 1987. PMID: 3313220 Review. No abstract available.

4

Stenotrophomonas maltophilia in cystic fibrosis: incidence and prevalence.

Demko CA, Stern RC, Doershuk CF. Demko CA, et al. Among authors: doershuk cf. Pediatr Pulmonol. 1998 May;25(5):304-8. doi: 10.1002/(sici)1099-0496(199805)25:5<304::aid-ppul3>3.0.co;2-i. Pediatr Pulmonol. 1998. PMID: 9635931

5

Pseudomonas cepacia: decrease in colonization in patients with cystic fibrosis.

Thomassen MJ, Demko CA, Doershuk CF, Stern RC, Klinger JD. Thomassen MJ, et al. Among authors: doershuk cf. Am Rev Respir Dis. 1986 Oct;134(4):669-71. doi: 10.1164/arrd.1986.134.4.669. Am Rev Respir Dis. 1986. PMID: 3767122

6

Colonization of the respiratory tract with Pseudomonas cepacia in cystic fibrosis. Risk factors and outcomes.

Tablan OC, Martone WJ, Doershuk CF, Stern RC, Thomassen MJ, Klinger JD, White JW, Carson LA, Jarvis WR. Tablan OC, et al. Among authors: doershuk cf. Chest. 1987 Apr;91(4):527-32. doi: 10.1378/chest.91.4.527. Chest. 1987. PMID: 3829745

7

Nontuberculous mycobacteria in cystic fibrosis. An autopsy study.

Tomashefski JF Jr, Stern RC, Demko CA, Doershuk CF. Tomashefski JF Jr, et al. Among authors: doershuk cf. Am J Respir Crit Care Med. 1996 Aug;154(2 Pt 1):523-8. doi: 10.1164/ajrccm.154.2.8756832. Am J Respir Crit Care Med. 1996. PMID: 8756832

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

An expanded scoring system including an index of nutritional status for patients with cystic fibrosis.

Cabrera ME, Lough MD, Doershuk CF, Salvator AE. Cabrera ME, et al. Among authors: doershuk cf. Pediatr Pulmonol. 1994 Oct;18(4):199-205. doi: 10.1002/ppul.1950180402. Pediatr Pulmonol. 1994. PMID: 7838617 Clinical Trial.

10

Cystic fibrosis: the prognosis for five-year survival.

Knoke JD, Stern RC, Doershuk CF, Boat TF, Matthews LW. Knoke JD, et al. Among authors: doershuk cf. Pediatr Res. 1978 May;12(5):676-9. doi: 10.1203/00006450-197805000-00012. Pediatr Res. 1978. PMID: 662472

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