Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 74

1.

Plasma metabolomics in adults with cystic fibrosis during a pulmonary exacerbation: A pilot randomized study of high-dose vitamin D3 administration.

Alvarez JA, Chong EY, Walker DI, Chandler JD, Michalski ES, Grossmann RE, Uppal K, Li S, Frediani JK, Tirouvanziam R, Tran VT, Tangpricha V, Jones DP, Ziegler TR.

Metabolism. 2017 May;70:31-41. doi: 10.1016/j.metabol.2017.02.006. Epub 2017 Feb 11.

PMID:
28403943
2.

Growth deficits in cystic fibrosis mice begin in utero prior to IGF-1 reduction.

Darrah R, Bederman I, Vitko M, Valerio DM, Drumm ML, Hodges CA.

PLoS One. 2017 Apr 6;12(4):e0175467. doi: 10.1371/journal.pone.0175467. eCollection 2017.

3.

Impact of CFTR Modulation on Intestinal pH, Motility, and Clinical Outcomes in Patients With Cystic Fibrosis and the G551D Mutation.

Gelfond D, Heltshe S, Ma C, Rowe SM, Frederick C, Uluer A, Sicilian L, Konstan M, Tullis E, Roach RN, Griffin K, Joseloff E, Borowitz D.

Clin Transl Gastroenterol. 2017 Mar 16;8(3):e81. doi: 10.1038/ctg.2017.10.

5.

Macronutrient intake in preschoolers with cystic fibrosis and the relationship between macronutrients and growth.

Filigno SS, Robson SM, Szczesniak RD, Chamberlin LA, Baker MA, Sullivan SM, Kroner J, Powers SW.

J Cyst Fibros. 2017 Jul;16(4):519-524. doi: 10.1016/j.jcf.2017.01.010. Epub 2017 Feb 6.

PMID:
28185886
6.

Growth in Prepubertal Children With Cystic Fibrosis Treated With Ivacaftor.

Stalvey MS, Pace J, Niknian M, Higgins MN, Tarn V, Davis J, Heltshe SL, Rowe SM.

Pediatrics. 2017 Feb;139(2). pii: e20162522. doi: 10.1542/peds.2016-2522.

7.

Lumacaftor/Ivacaftor in Patients Aged 6-11 Years with Cystic Fibrosis and Homozygous for F508del-CFTR.

Milla CE, Ratjen F, Marigowda G, Liu F, Waltz D, Rosenfeld M; VX13-809-011 Part B Investigator Group * .

Am J Respir Crit Care Med. 2017 Apr 1;195(7):912-920. doi: 10.1164/rccm.201608-1754OC.

PMID:
27805836
8.

Exercise capacity following a percutaneous endoscopic gastrostomy in a young female with cystic fibrosis: a case report.

Tomlinson OW, Barker AR, Oades PJ, Williams CA.

Physiol Rep. 2016 Aug;4(16). pii: e12904. Epub 2016 Aug 22.

9.

Background and Epidemiology.

Sanders DB, Fink AK.

Pediatr Clin North Am. 2016 Aug;63(4):567-84. doi: 10.1016/j.pcl.2016.04.001. Review.

PMID:
27469176
10.

Gastrointestinal Manifestations of Cystic Fibrosis.

Sabharwal S.

Gastroenterol Hepatol (N Y). 2016 Jan;12(1):43-7.

11.

Young adults with cystic fibrosis have altered trabecular microstructure by ITS-based morphological analysis.

Putman MS, Greenblatt LB, Sicilian L, Uluer A, Lapey A, Sawicki G, Gordon CM, Bouxsein ML, Finkelstein JS.

Osteoporos Int. 2016 Aug;27(8):2497-505. doi: 10.1007/s00198-016-3557-z. Epub 2016 Mar 7.

PMID:
26952010
12.

Digestive Enzyme Supplementation in Gastrointestinal Diseases.

Ianiro G, Pecere S, Giorgio V, Gasbarrini A, Cammarota G.

Curr Drug Metab. 2016;17(2):187-93. Review.

13.

Body composition and lung function in cystic fibrosis and their association with adiposity and normal-weight obesity.

Alvarez JA, Ziegler TR, Millson EC, Stecenko AA.

Nutrition. 2016 Apr;32(4):447-52. doi: 10.1016/j.nut.2015.10.012. Epub 2015 Oct 30.

14.

Parental Depression and Pancreatic Enzymes Adherence in Children With Cystic Fibrosis.

Barker DH, Quittner AL.

Pediatrics. 2016 Feb;137(2):e20152296. doi: 10.1542/peds.2015-2296. Epub 2016 Jan 5.

15.

Web-Based Intervention for Nutritional Management in Cystic Fibrosis: Development, Usability, and Pilot Trial.

Stark LJ, Opipari-Arrigan L, Filigno SS, Simon SL, Leonard A, Mogayzel PJ, Rausch J, Zion C, Powers SW.

J Pediatr Psychol. 2016 Jun;41(5):510-21. doi: 10.1093/jpepsy/jsv108. Epub 2015 Nov 18.

16.

Adherence to airway clearance therapy in pediatric cystic fibrosis: Socioeconomic factors and respiratory outcomes.

Oates GR, Stepanikova I, Gamble S, Gutierrez HH, Harris WT.

Pediatr Pulmonol. 2015 Dec;50(12):1244-52. doi: 10.1002/ppul.23317. Epub 2015 Oct 5.

17.

Sleep-disordered breathing in patients with cystic fibrosis.

Veronezi J, Carvalho AP, Ricachinewsky C, Hoffmann A, Kobayashi DY, Piltcher OB, Abreu e Silva FA, Martinez D.

J Bras Pneumol. 2015 Jul-Aug;41(4):351-7. doi: 10.1590/S1806-37132015000004468. English, Portuguese.

18.

Early Life Growth Trajectories in Cystic Fibrosis are Associated with Pulmonary Function at Age 6 Years.

Sanders DB, Fink A, Mayer-Hamblett N, Schechter MS, Sawicki GS, Rosenfeld M, Flume PA, Morgan WJ.

J Pediatr. 2015 Nov;167(5):1081-8.e1. doi: 10.1016/j.jpeds.2015.07.044. Epub 2015 Sep 2.

19.
20.

Nutritional status of adolescents with cystic fibrosis treated at a reference center in the southeast region of Brazil.

Del Ciampo IR, Del Ciampo LA, Sawamura R, de Oliveira LR, Fernandes MI.

Ital J Pediatr. 2015 Jul 30;41:51. doi: 10.1186/s13052-015-0159-x.

Supplemental Content

Support Center