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Items: 1 to 20 of 762

1.

Mucosal Autoimmunity to Cell-Bound GP2 Isoforms Is a Sensitive Marker in PSC and Associated With the Clinical Phenotype.

Sowa M, Kolenda R, Baumgart DC, Pratschke J, Papp M, Tornai T, Suchanski J, Bogdanos DP, Mytilinaiou MG, Hammermann J, Laass MW, Conrad K, Schramm C, Franke A, Roggenbuck D, Schierack P.

Front Immunol. 2018 Aug 28;9:1959. doi: 10.3389/fimmu.2018.01959. eCollection 2018.

2.

Feasibility and diagnostic accuracy of an electronic nose in children with asthma and cystic fibrosis.

Bannier MAGE, van de Kant KDG, Jöbsis Q, Dompeling E.

J Breath Res. 2018 Sep 14. doi: 10.1088/1752-7163/aae158. [Epub ahead of print]

PMID:
30213921
3.

Quantitative Assessment of Cyanide in Cystic Fibrosis Sputum and its Oxidative Catabolism by Hypochlorous Acid.

Eiserich JP, Ott SP, Kadir T, Morrissey BM, Hayakawa KA, La Merrill MA, Cross CE.

Free Radic Biol Med. 2018 Sep 10. pii: S0891-5849(18)31406-0. doi: 10.1016/j.freeradbiomed.2018.09.007. [Epub ahead of print]

PMID:
30213640
4.

Cystic Fibrosis-Related Diabetes Screening in Adults: A Gap Analysis and Evaluation of Accuracy of Glycated Hemoglobin Levels.

Gilmour JA, Sykes J, Etchells E, Tullis E.

Can J Diabetes. 2018 May 2. pii: S1499-2671(18)30114-X. doi: 10.1016/j.jcjd.2018.04.008. [Epub ahead of print]

PMID:
30173928
5.

Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands.

Dankert-Roelse JE, Bouva MJ, Jakobs BS, Janssens HM, de Winter-de Groot KM, Schönbeck Y, Gille JJP, Gulmans VAM, Verschoof-Puite RK, Schielen PCJI, Verkerk PH.

J Cyst Fibros. 2018 Aug 23. pii: S1569-1993(18)30705-7. doi: 10.1016/j.jcf.2018.07.008. [Epub ahead of print]

PMID:
30146269
6.

Profiling of Bacterial and Fungal Microbial Communities in Cystic Fibrosis Sputum Using RNA.

Grahl N, Dolben EL, Filkins LM, Crocker AW, Willger SD, Morrison HG, Sogin ML, Ashare A, Gifford AH, Jacobs NJ, Schwartzman JD, Hogan DA.

mSphere. 2018 Aug 8;3(4). pii: e00292-18. doi: 10.1128/mSphere.00292-18.

7.

Virtual Screening Against Carbohydrate-Binding Proteins: Evaluation and Application to Bacterial Burkholderia ambifaria Lectin.

Dingjan T, Gillon É, Imberty A, Pérez S, Titz A, Ramsland PA, Yuriev E.

J Chem Inf Model. 2018 Sep 4. doi: 10.1021/acs.jcim.8b00185. [Epub ahead of print]

PMID:
30075071
8.

The Efficacy of MRI in the diagnostic workup of cystic fibrosis-associated liver disease: A clinical observational cohort study.

Poetter-Lang S, Staufer K, Baltzer P, Tamandl D, Muin D, Bastati N, Halilbasic E, Hodge JC, Trauner M, Kazemi-Shirazi L, Ba-Ssalamah A.

Eur Radiol. 2018 Jul 27. doi: 10.1007/s00330-018-5650-5. [Epub ahead of print]

PMID:
30054796
9.

miRNA-Seq identifies a serum miRNA panel, which combined with APRI can detect and monitor liver disease in paediatric Cystic Fibrosis.

Calvopina DA, Chatfield MD, Weis A, Coleman MA, Fernandez-Rojo MA, Noble C, Ramm LE, Leung DH, Lewindon PJ, Ramm GA.

Hepatology. 2018 Jul 16. doi: 10.1002/hep.30156. [Epub ahead of print]

PMID:
30014495
10.

Results of the Andalusian Cystic Fibrosis Neonatal Screening Program, 5 Years After Implementation.

Delgado Pecellín I, Pérez Ruiz E, Álvarez Ríos AI, Delgado Pecellín C, Yahyaoui Macías R, Carrasco Hernández L, Marcos Luque I, Caro Aguilera P, Moreno Valera MJ, Quintana Gallego ME.

Arch Bronconeumol. 2018 Jul 5. pii: S0300-2896(18)30162-5. doi: 10.1016/j.arbres.2018.03.013. [Epub ahead of print] English, Spanish.

11.

The anti-adhesive effect of glycoclusters on Pseudomonas aeruginosa bacteria adhesion to epithelial cells studied by AFM single cell force spectroscopy.

Zuttion F, Ligeour C, Vidal O, Wälte M, Morvan F, Vidal S, Vasseur JJ, Chevolot Y, Phaner-Goutorbe M, Schillers H.

Nanoscale. 2018 Jul 9;10(26):12771-12778. doi: 10.1039/c8nr03285h.

PMID:
29946584
12.

Ciliated conical epithelial cell protrusions point towards a diagnosis of primary ciliary dyskinesia.

O'Callaghan C, Rutman A, Williams G, Kulkarni N, Hayes J, Hirst RA.

Respir Res. 2018 Jun 25;19(1):125. doi: 10.1186/s12931-018-0782-3.

13.

Utility of recombinant Aspergillus fumigatus antigens in the diagnosis of allergic bronchopulmonary aspergillosis: A systematic review and diagnostic test accuracy meta-analysis.

Muthu V, Sehgal IS, Dhooria S, Aggarwal AN, Agarwal R.

Clin Exp Allergy. 2018 Sep;48(9):1107-1136. doi: 10.1111/cea.13216. Epub 2018 Jul 24. Review.

PMID:
29927507
14.

Performance Evaluation of a New Coulometric Endpoint Method in Sweat Testing and Its Comparison With Classic Gibson&Cooke and Chloridometer Methods in Cystic Fibrosis.

Gokdemir Y, Vatansever P, Karadag B, Seyrekel T, Baykan O, Bas Ikızoglu N, Ersu R, Karakoc F, Haklar G.

Front Pediatr. 2018 May 22;6:133. doi: 10.3389/fped.2018.00133. eCollection 2018.

15.
16.

An Enzyme Immunoassay for Determining Immunoreactive Trypsinogen (IRT) in Dried Blood Spots on Filter Paper Using an Ultra-Microanalytical System.

Castells Martínez EM, González EC, Tejeda Y, Frómeta A, Martín O, Espinosa M, Del Río L, Pérez PL, Morejón G, Perea Y, Melchor A.

Appl Biochem Biotechnol. 2018 May 29. doi: 10.1007/s12010-018-2785-4. [Epub ahead of print]

PMID:
29808455
17.

Analysis of Phylogenetic Variation of Stenotrophomonas maltophilia Reveals Human-Specific Branches.

Steinmann J, Mamat U, Abda EM, Kirchhoff L, Streit WR, Schaible UE, Niemann S, Kohl TA.

Front Microbiol. 2018 Apr 26;9:806. doi: 10.3389/fmicb.2018.00806. eCollection 2018.

18.

Comparison of folate-conjugated rapamycin versus unconjugated rapamycin in an orthologous mouse model of polycystic kidney disease.

Kipp KR, Kruger SL, Schimmel MF, Parker N, Shillingford JM, Leamon CP, Weimbs T.

Am J Physiol Renal Physiol. 2018 Aug 1;315(2):F395-F405. doi: 10.1152/ajprenal.00057.2018. Epub 2018 May 2.

PMID:
29717938
19.

The clinical significance of oropharyngeal cultures in young children with cystic fibrosis.

Breuer O, Caudri D, Akesson L, Ranganathan S, Stick SM, Schultz A; AREST CF.

Eur Respir J. 2018 May 17;51(5). pii: 1800238. doi: 10.1183/13993003.00238-2018. Print 2018 May.

PMID:
29678944
20.

Establishing the diagnosis of chronic colonization with Pseudomonas aeruginosa of cystic fibrosis patients: Comparison of the European consensus criteria with genotyping of P. aeruginosa isolates.

Jonckheere L, Schelstraete P, Van Simaey L, Van Braeckel E, Willekens J, Van Daele S, De Baets F, Vaneechoutte M.

J Cyst Fibros. 2018 Apr 11. pii: S1569-1993(18)30074-2. doi: 10.1016/j.jcf.2018.03.004. [Epub ahead of print]

PMID:
29655935

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