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Items: 1 to 20 of 57

1.

Novel Inhalable Ciprofloxacin Dry Powders for Bronchiectasis Therapy: Mannitol-Silk Fibroin Binary Microparticles with High-Payload and Improved Aerosolized Properties.

Liu C, Lin L, Huang Z, Wu Q, Jiang J, Lv L, Yu X, Quan G, Li G, Wu C.

AAPS PharmSciTech. 2019 Jan 23;20(2):85. doi: 10.1208/s12249-019-1291-5.

PMID:
30673901
2.

A safety lancet for neonatal blood spot tests: a design that facilitates pain-free, atraumatic samples.

Goodwin S, Supachana N.

Br J Nurs. 2019 Jan 24;28(2):S24-S28. doi: 10.12968/bjon.2019.28.2.S24.

PMID:
30673311
3.

Arthropathy and Cutaneous Eruption in a Patient With Cystic Fibrosis.

Luu LA, Guffey DJ, Zlotoff BJ.

JAMA Dermatol. 2019 Jan 23. doi: 10.1001/jamadermatol.2018.5018. [Epub ahead of print] No abstract available.

PMID:
30673074
4.

Nocturnal oximetry in children with obstructive lung disease or sleep-disordered breathing.

Katsouli G, Polytarchou A, Tsaoussoglou M, Loukou I, Chrousos G, Kaditis AG.

Pediatr Pulmonol. 2019 Jan 22. doi: 10.1002/ppul.24259. [Epub ahead of print]

PMID:
30672145
5.

Pulmonary findings in infants with cystic fibrosis during the first year of life: Results from the Baby Observational and Nutrition Study (BONUS) cohort study.

Goetz D, Kopp BT, Salvator A, Moore-Clingenpeel M, McCoy K, Leung DH, Kloster M, Ramsey BR, Heltshe SH, Borowitz D.

Pediatr Pulmonol. 2019 Jan 22. doi: 10.1002/ppul.24261. [Epub ahead of print]

PMID:
30672141
6.

Reframing health and illness: a collaborative autoethnography on the experience of health and illness transformations in the life course.

Nowakowski ACH, Sumerau JE.

Sociol Health Illn. 2019 Jan 22. doi: 10.1111/1467-9566.12849. [Epub ahead of print]

PMID:
30671982
7.

Histone Acetylation Promotes Neutrophil Extracellular Trap Formation.

Hamam HJ, Khan MA, Palaniyar N.

Biomolecules. 2019 Jan 18;9(1). pii: E32. doi: 10.3390/biom9010032.

PMID:
30669408
8.

A defective flexible loop contributes to the processing and gating defects of the predominant cystic fibrosis-causing mutation.

Chen X, Zhu S, Zhenin M, Xu W, Bose SJ, Wong MP, Leung GPH, Senderowitz H, Chen JH.

FASEB J. 2019 Jan 22:fj201801218RR. doi: 10.1096/fj.201801218RR. [Epub ahead of print]

PMID:
30668920
9.

Cost Effectiveness of Inhaled Mannitol (Bronchitol®) in Patients with Cystic Fibrosis.

Warren E, Morgan K, Toward TJ, Schwenkglenks M, Leadbetter J.

Pharmacoeconomics. 2019 Jan 22. doi: 10.1007/s40273-019-00767-8. [Epub ahead of print]

PMID:
30666534
10.

Molecular characterization of the pilS2 gene and its association with the frequency of Pseudomonas aeruginosa plasmid pKLC102 and PAPI-1 pathogenicity island.

Bahramian A, Khoshnood S, Shariati A, Doustdar F, Chirani AS, Heidary M.

Infect Drug Resist. 2019 Jan 11;12:221-227. doi: 10.2147/IDR.S188527. eCollection 2019.

PMID:
30666137
11.

Visceral adipose tissue is associated with poor diet quality and higher fasting glucose in adults with cystic fibrosis.

Bellissimo MP, Zhang I, Ivie EA, Tran PH, Tangpricha V, Hunt WR, Stecenko AA, Ziegler TR, Alvarez JA.

J Cyst Fibros. 2019 Jan 18. pii: S1569-1993(18)30812-9. doi: 10.1016/j.jcf.2019.01.002. [Epub ahead of print]

PMID:
30665857
12.

Lack of GAS2L2 Causes PCD by Impairing Cilia Orientation and Mucociliary Clearance.

Bustamante-Marin XM, Yin WN, Sears PR, Werner ME, Brotslaw EJ, Mitchell BJ, Jania CM, Zeman KL, Rogers TD, Herring LE, Refabért L, Thomas L, Amselem S, Escudier E, Legendre M, Grubb BR, Knowles MR, Zariwala MA, Ostrowski LE.

Am J Hum Genet. 2019 Jan 18. pii: S0002-9297(18)30460-9. doi: 10.1016/j.ajhg.2018.12.009. [Epub ahead of print]

PMID:
30665704
13.

An evaluation of methods for the isolation of nontuberculous mycobacteria from patients with cystic fibrosis, bronchiectasis and patients assessed for lung transplantation.

Stephenson D, Perry A, Appleby MR, Lee D, Davison J, Johnston A, Jones AL, Nelson A, Bourke SJ, Thomas MF, De Soyza A, Lordan JL, Lumb J, Robb AE, Samuel JR, Walton KE, Perry JD.

BMC Pulm Med. 2019 Jan 21;19(1):19. doi: 10.1186/s12890-019-0781-2.

PMID:
30665395
14.

Penicillin binding protein 3 is a common adaptive target among Pseudomonas aeruginosa isolates from adult cystic fibrosis patients treated with β-lactams.

Clark ST, Sinha U, Zhang Y, Wang PW, Donaldson SL, Coburn B, Waters VJ, Yau YCW, Tullis DE, Guttman DS, Hwang DM.

Int J Antimicrob Agents. 2019 Jan 18. pii: S0924-8579(19)30009-3. doi: 10.1016/j.ijantimicag.2019.01.009. [Epub ahead of print]

PMID:
30664925
15.

Lung Allocation Score Thresholds Prioritize Survival after Lung Transplantation.

Li SS, Miller R, Tumin D, Stewart WCL, Tobias JD, Hayes D Jr.

Chest. 2019 Jan 18. pii: S0012-3692(19)30023-6. doi: 10.1016/j.chest.2019.01.008. [Epub ahead of print]

PMID:
30664859
16.

Anaerobes in cystic fibrosis patients' airways.

Lamoureux C, Guilloux CA, Beauruelle C, Jolivet-Gougeon A, Héry-Arnaud G.

Crit Rev Microbiol. 2019 Jan 21:1-15. doi: 10.1080/1040841X.2018.1549019. [Epub ahead of print]

PMID:
30663924
17.

CF derived scoring systems do not fully describe the range of structural changes seen on CT scans in PCD.

Tadd K, Morgan L, Rosenow T, Schultz A, Susanto C, Murray C, Robinson P.

Pediatr Pulmonol. 2019 Jan 21. doi: 10.1002/ppul.24249. [Epub ahead of print]

PMID:
30663844
18.

Lung disease and vitamin D levels in cystic fibrosis infants and preschoolers.

Oliveira MS, Matsunaga NY, Rodrigues MLE, Morcillo AM, de Oliveira Ribeiro MAG, Ribeiro AF, de Fátima C P Servidoni M, Nogueira RJN, Pereira MC, Ribeiro JD, Toro AADC.

Pediatr Pulmonol. 2019 Jan 20. doi: 10.1002/ppul.24260. [Epub ahead of print]

PMID:
30663283
19.

Secondhand smoke alters arachidonic acid metabolism and inflammation in infants and children with cystic fibrosis.

Kopp BT, Thompson R, Kim J, Konstan R, Diaz A, Smith B, Shrestha C, Rogers LK, Hayes D Jr, Tumin D, Woodley FW, Ramilo O, Sanders DB, Groner JA, Mejias A.

Thorax. 2019 Jan 19. pii: thoraxjnl-2018-211845. doi: 10.1136/thoraxjnl-2018-211845. [Epub ahead of print]

PMID:
30661024
20.

Cystic fibrosis: a call for papers for ECFS 2019.

Grainger E.

Lancet Respir Med. 2019 Jan 16. pii: S2213-2600(19)30007-4. doi: 10.1016/S2213-2600(19)30007-4. [Epub ahead of print] No abstract available.

PMID:
30660510

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