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Items: 1 to 20 of 95

1.

Subclinical Left Ventricular Dysfunction is Influenced by Genotype Severity in Patients with Cystic Fibrosis.

Pallin M, Keating D, Kaye DM, Kotsimbos T, Wilson JW.

Clin Med Insights Circ Respir Pulm Med. 2018 Aug 19;12:1179548418794154. doi: 10.1177/1179548418794154. eCollection 2018.

2.

CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.

Bonadia LC, de Lima Marson FA, Ribeiro JD, Paschoal IA, Pereira MC, Ribeiro AF, Bertuzzo CS.

Gene. 2014 May 1;540(2):183-90. doi: 10.1016/j.gene.2014.02.040. Epub 2014 Feb 26.

PMID:
24583165
3.

[Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].

Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.

Srp Arh Celok Lek. 2001 May-Jun;129 Suppl 1:6-9. Serbian.

PMID:
15637983
4.

Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.

De Boeck K, Weren M, Proesmans M, Kerem E.

Pediatrics. 2005 Apr;115(4):e463-9. Epub 2005 Mar 16.

PMID:
15772171
5.

CFTR Cl- channel function in native human colon correlates with the genotype and phenotype in cystic fibrosis.

Hirtz S, Gonska T, Seydewitz HH, Thomas J, Greiner P, Kuehr J, Brandis M, Eichler I, Rocha H, Lopes AI, Barreto C, Ramalho A, Amaral MD, Kunzelmann K, Mall M.

Gastroenterology. 2004 Oct;127(4):1085-95.

PMID:
15480987
6.

Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in pancreatitis.

Ooi CY, Durie PR.

J Cyst Fibros. 2012 Sep;11(5):355-62. doi: 10.1016/j.jcf.2012.05.001. Epub 2012 Jun 2. Review.

7.

Applying Cystic Fibrosis Transmembrane Conductance Regulator Genetics and CFTR2 Data to Facilitate Diagnoses.

Sosnay PR, Salinas DB, White TB, Ren CL, Farrell PM, Raraigh KS, Girodon E, Castellani C.

J Pediatr. 2017 Feb;181S:S27-S32.e1. doi: 10.1016/j.jpeds.2016.09.063.

PMID:
28129809
8.

Technological advances shed light on left ventricular cardiac disturbances in cystic fibrosis.

Sayyid ZN, Sellers ZM.

J Cyst Fibros. 2017 Jul;16(4):454-464. doi: 10.1016/j.jcf.2017.02.013. Epub 2017 Mar 14. Review.

PMID:
28314540
9.

Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data.

Derichs N, Sanz J, Von Kanel T, Stolpe C, Zapf A, Tümmler B, Gallati S, Ballmann M.

Thorax. 2010 Jul;65(7):594-9. doi: 10.1136/thx.2009.125088.

PMID:
20627915
10.

ENaCbeta and gamma genes as modifier genes in cystic fibrosis.

Viel M, Leroy C, Hubert D, Fajac I, Bienvenu T.

J Cyst Fibros. 2008 Jan;7(1):23-9. Epub 2007 Jun 7.

11.

Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

Bienvenu T, Sermet-Gaudelus I, Burgel PR, Hubert D, Crestani B, Bassinet L, Dusser D, Fajac I.

Am J Respir Crit Care Med. 2010 May 15;181(10):1078-84. doi: 10.1164/rccm.200909-1434OC. Epub 2010 Feb 18.

PMID:
20167849
12.

Strain rate echocardiography uncovers subclinical left ventricular dysfunction in cystic fibrosis.

Sellers ZM, McGlocklin L, Brasch A.

J Cyst Fibros. 2015 Sep;14(5):654-60. doi: 10.1016/j.jcf.2015.03.010. Epub 2015 Apr 9.

13.
14.

Variants in the glutamate-cysteine-ligase gene are associated with cystic fibrosis lung disease.

McKone EF, Shao J, Frangolias DD, Keener CL, Shephard CA, Farin FM, Tonelli MR, Pare PD, Sandford AJ, Aitken ML, Kavanagh TJ.

Am J Respir Crit Care Med. 2006 Aug 15;174(4):415-9. Epub 2006 May 11.

15.

Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.

Ferril GR, Nick JA, Getz AE, Barham HP, Saavedra MT, Taylor-Cousar JL, Nichols DP, Curran-Everett D, Kingdom TT, Ramakrishnan VR.

Int Forum Allergy Rhinol. 2014 Nov;4(11):915-20. doi: 10.1002/alr.21412. Epub 2014 Sep 15.

PMID:
25224556
16.

IL1B polymorphisms modulate cystic fibrosis lung disease.

Levy H, Murphy A, Zou F, Gerard C, Klanderman B, Schuemann B, Lazarus R, García KC, Celedón JC, Drumm M, Dahmer M, Quasney M, Schneck K, Reske M, Knowles MR, Pier GB, Lange C, Weiss ST.

Pediatr Pulmonol. 2009 Jun;44(6):580-93. doi: 10.1002/ppul.21026.

17.

Genotype and phenotype in cystic fibrosis.

Zielenski J.

Respiration. 2000;67(2):117-33. Review.

PMID:
10773783
18.

Genotype-phenotype relationships in a cohort of adult cystic fibrosis patients.

Hubert D, Bienvenu T, Desmazes-Dufeu N, Fajac I, Lacronique J, Matran R, Kaplan JC, Dusser DJ.

Eur Respir J. 1996 Nov;9(11):2207-14.

19.

Genotype-phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles.

Terlizzi V, Castaldo G, Salvatore D, Lucarelli M, Raia V, Angioni A, Carnovale V, Cirilli N, Casciaro R, Colombo C, Di Lullo AM, Elce A, Iacotucci P, Comegna M, Scorza M, Lucidi V, Perfetti A, Cimino R, Quattrucci S, Seia M, Sofia VM, Zarrilli F, Amato F.

J Med Genet. 2017 Apr;54(4):224-235. doi: 10.1136/jmedgenet-2016-103985. Epub 2016 Oct 13.

20.

Analysis of exocrine pancreatic function in cystic fibrosis: one mild CFTR mutation does not exclude pancreatic insufficiency.

Walkowiak J, Herzig KH, Witt M, Pogorzelski A, Piotrowski R, Barra E, Sobczynska-Tomaszewska A, Trawinska-Bartnicka M, Strzykala K, Cichy W, Sands D, Rutkiewicz E, Krawczynski M.

Eur J Clin Invest. 2001 Sep;31(9):796-801.

PMID:
11589722

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