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Items: 1 to 20 of 82

1.

Relapse of chronic melioidosis in a paediatric cystic fibrosis patient: first case report from Malaysia.

Mariappan V, Thavagnanam S, Vellasamy KM, Teh CJS, Atiya N, Ponnampalavanar S, Vadivelu J.

BMC Infect Dis. 2018 Sep 5;18(1):455. doi: 10.1186/s12879-018-3371-7.

2.

Hospitalization costs of cystic fibrosis in the United States: a retrospective analysis.

Vadagam P, Kamal KM.

Hosp Pract (1995). 2018 Oct;46(4):203-213. doi: 10.1080/21548331.2018.1505407. Epub 2018 Aug 9.

PMID:
30067115
3.

V232D mutation in patients with cystic fibrosis: Not so rare, not so mild.

Fernández-Lorenzo AE, Moreno-Álvarez A, Colon-Mejeras C, Barros-Angueira F, Solar-Boga A, Sirvent-Gómez J, Couce ML, Leis R.

Medicine (Baltimore). 2018 Jul;97(28):e11397. doi: 10.1097/MD.0000000000011397.

4.

Respiratory muscle training for cystic fibrosis.

Hilton N, Solis-Moya A.

Cochrane Database Syst Rev. 2018 May 24;5:CD006112. doi: 10.1002/14651858.CD006112.pub4. Review.

PMID:
29797578
5.

Case Study: Cystic Fibrosis in the Newborn.

Saravia PA, Riley C.

Neonatal Netw. 2018 May 1;37(3):164-168. doi: 10.1891/0730-0832.37.3.164.

PMID:
29789057
6.

Coping with stress by mothers of children and adolescents with cystic fibrosis.

Zubrzycka R.

Adv Respir Med. 2018;86(2):86-91. doi: 10.5603/ARM.2018.0011.

7.

The Swiss Cystic Fibrosis Infant Lung Development (SCILD) cohort.

Korten I, Kieninger E, Yammine S, Regamey N, Nyilas S, Ramsey K, Casaulta C, Latzin P, For The Scild Study Group.

Swiss Med Wkly. 2018 Apr 26;148:w14618. doi: 10.4414/smw.2018.14618. eCollection 2018.

8.

Hemoglobin A1c Accurately Predicts Continuous Glucose Monitoring-Derived Average Glucose in Youth and Young Adults With Cystic Fibrosis.

Chan CL, Hope E, Thurston J, Vigers T, Pyle L, Zeitler PS, Nadeau KJ.

Diabetes Care. 2018 Jul;41(7):1406-1413. doi: 10.2337/dc17-2419. Epub 2018 Apr 19.

PMID:
29674323
9.

Use of an In-line Digestive Cartridge With Enteral Nutrition Improves the Weight Trajectory of 2 Children With Cystic Fibrosis Complicated by Another Medical Diagnosis.

Giguere-Rich C, Mathew A, Reid E, Autore K, Guill MF.

Nutr Clin Pract. 2018 Apr;33(2):286-294. doi: 10.1002/ncp.10080.

PMID:
29658186
10.

Evaluating Changes in Handgrip Strength in Children With Cystic Fibrosis: A Pilot Study.

Gibson HT, McDonald CM, Derrick JW, Eggett DL, Bellini SG.

Nutr Clin Pract. 2018 Apr;33(2):261-267. doi: 10.1002/ncp.10067.

PMID:
29658185
11.

ETHICS EVALUATION REVEALING DECISION-MAKER MOTIVES: A CASE OF NEONATAL SCREENING.

Raimond V, Sambuc C, Pibouleau L.

Int J Technol Assess Health Care. 2018 Jan;34(2):189-195. doi: 10.1017/S0266462318000181. Epub 2018 Apr 10.

PMID:
29633672
12.

Validation of automated lobe segmentation on paired inspiratory-expiratory chest CT in 8-14 year-old children with cystic fibrosis.

Konietzke P, Weinheimer O, Wielpütz MO, Savage D, Ziyeh T, Tu C, Newman B, Galbán CJ, Mall MA, Kauczor HU, Robinson TE.

PLoS One. 2018 Apr 9;13(4):e0194557. doi: 10.1371/journal.pone.0194557. eCollection 2018.

13.

Implementing carrier screening for cystic fibrosis outside the clinic: ethical analysis in the light of the personalist view.

Di Pietro ML, Teleman AA, Gonzalez-Melado FJ, Zace D, Di Raimo FR, Lucidi V, Refolo P.

Clin Ter. 2018 Mar-Apr;169(2):e71-e76. doi: 10.7417/T.2018.2057.

14.

Non-contrast enhanced magnetic resonance imaging detects mosaic signal intensity in early cystic fibrosis lung disease.

Leutz-Schmidt P, Stahl M, Sommerburg O, Eichinger M, Puderbach MU, Schenk JP, Alrajab A, Triphan SMF, Kauczor HU, Mall MA, Wielpütz MO.

Eur J Radiol. 2018 Apr;101:178-183. doi: 10.1016/j.ejrad.2018.02.023. Epub 2018 Feb 21.

PMID:
29571794
15.

Burkholderia cepacia, cystic fibrosis and outcomes following lung transplantation: experiences from a single center in Brazil.

de Souza Carraro D, Carraro RM, Campos SV, Iuamoto LR, Braga KAO, Oliveira LC, Sabino EC, Rossi F, Pêgo-Fernandes PM.

Clinics (Sao Paulo). 2018 Mar 12;73:e166. doi: 10.6061/clinics/2018/e166.

16.

Exploring the need for Transition Readiness Scales within cystic fibrosis services: A qualitative descriptive study.

Bourke M, Houghton C.

J Clin Nurs. 2018 Jul;27(13-14):2814-2824. doi: 10.1111/jocn.14344. Epub 2018 Apr 19.

PMID:
29516552
17.

Hyperthyrotropinemia in newly diagnosed cystic fibrosis patients with pancreatic insufficiency reversed by enzyme therapy.

Giannakopoulos A, Katelaris A, Noni M, Karakonstantakis T, Kanaka-Gantenbein C, Doudounakis S.

Eur J Pediatr. 2018 May;177(5):775-779. doi: 10.1007/s00431-018-3120-3. Epub 2018 Feb 27.

PMID:
29487998
18.

Islet Interleukin-1β Immunoreactivity Is an Early Feature of Cystic Fibrosis That May Contribute to β-Cell Failure.

Hull RL, Gibson RL, McNamara S, Deutsch GH, Fligner CL, Frevert CW, Ramsey BW, Sanda S.

Diabetes Care. 2018 Apr;41(4):823-830. doi: 10.2337/dc17-1387. Epub 2018 Feb 1.

PMID:
29437698
19.

Inhaled mannitol for cystic fibrosis.

Nevitt SJ, Thornton J, Murray CS, Dwyer T.

Cochrane Database Syst Rev. 2018 Feb 9;2:CD008649. doi: 10.1002/14651858.CD008649.pub3. Review.

PMID:
29424930
20.

Peripheral quantitative computed tomography detects differences at the radius in prepubertal children with cystic fibrosis compared to healthy controls.

O'Brien CE, Com G, Fowlkes J, Tang X, James LP.

PLoS One. 2018 Jan 11;13(1):e0191013. doi: 10.1371/journal.pone.0191013. eCollection 2018.

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