SOCIEDAD ECUATORIANA DE TISIOLOGÍA Y ENFERMEDADES DEL TÓRAX

NOTICIAS

 

ASSOCIACIÓ CATALANA DE FIBROSI QUÍSTICA

13/04/2019

Citas bibliográficas entradas en PubMed desde 06/04/2019

 Criterio de filtrado "cystic fibrosis"

 

Items 1 - 55

 

1.

Results from an online survey of adults with cystic fibrosis: Accessing and using life expectancy information.

Keogh RH, Bilton D, Cosgriff R, Kavanagh D, Rayner O, Sedgwick PM.

PLoS One. 2019 Apr 12;14(4):e0213639. doi: 10.1371/journal.pone.0213639. eCollection 2019.

PMID: 30978192 [PubMed - in process]

 

2.

Signalling Effects Induced by Acid Ceramidase in Human Epithelial Or Leukemic Cell Lines.

Baduva K, Büchter L, Kreyenkamp K, Westphal L, Wilker B, Kohnen M, Schuchman EH, Edwards MJ, Becker KA, Gulbins E, Carpinteiro A.

Cell Physiol Biochem. 2019;52(5):1092-1102. doi: 10.33594/000000074.

PMID: 30977990 [PubMed - in process]

 

3.

Caffeine Accelerates Cystic Kidney Disease in a Pkd1-Deficient Mouse Model.

Meca R, Balbo BE, Ormanji MS, Fonseca JM, Iannuzzi LR, Santana Costa E, Onuchic LF, Heilberg IP.

Cell Physiol Biochem. 2019;52(5):1061-1074. doi: 10.33594/000000072.

PMID: 30977988 [PubMed - in process]

 

4.

lptG contributes to changes in membrane permeability and the emergence of multidrug hypersusceptibility in a cystic fibrosis isolate of Pseudomonas aeruginosa.

Harrison LB, Fowler RC, Abdalhamid B, Selmecki A, Hanson ND.

Microbiologyopen. 2019 Apr 12:e844. doi: 10.1002/mbo3.844. [Epub ahead of print]

PMID: 30977288 [PubMed - as supplied by publisher]

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5.

Transcytosis maintains CFTR apical polarity in the face of constitutive and mutation-induced basolateral missorting.

Bidaud-Meynard A, Bossard F, Schnúr A, Fukuda R, Veit G, Xu H, Lukacs GL.

J Cell Sci. 2019 Apr 11. pii: jcs.226886. doi: 10.1242/jcs.226886. [Epub ahead of print]

PMID: 30975917 [PubMed - as supplied by publisher]

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6.

Reply - Cystic fibrosis complicated by cor pulmonale: The first case report in Taiwan.

Shyur SD.

Pediatr Neonatol. 2019 Mar 26. pii: S1875-9572(19)30105-6. doi: 10.1016/j.pedneo.2019.03.009. [Epub ahead of print] No abstract available.

PMID: 30975616 [PubMed - as supplied by publisher]

Similar articles

 

7.

Cystic fibrosis complicated by cor pulmonale: The first case report in Taiwan.

Moslehi MA.

Pediatr Neonatol. 2019 Mar 26. pii: S1875-9572(19)30056-7. doi: 10.1016/j.pedneo.2019.03.008. [Epub ahead of print] No abstract available.

PMID: 30975615 [PubMed - as supplied by publisher]

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8.

"Fortunate are those who take the first steps"? The psychosocial impact of novel drug development.

Dobra R, Madge S, Martin I, Weldon P, Simmonds N, Davies JC.

Paediatr Respir Rev. 2019 Feb 27. pii: S1526-0542(19)30019-3. doi: 10.1016/j.prrv.2019.02.005. [Epub ahead of print] Review.

PMID: 30975518 [PubMed - as supplied by publisher]

Similar articles

 

9.

Functional effects of the microbiota in chronic respiratory disease.

Budden KF, Shukla SD, Rehman SF, Bowerman KL, Keely S, Hugenholtz P, Armstrong-James DPH, Adcock IM, Chotirmall SH, Chung KF, Hansbro PM.

Lancet Respir Med. 2019 Apr 8. pii: S2213-2600(18)30510-1. doi: 10.1016/S2213-2600(18)30510-1. [Epub ahead of print] Review.

PMID: 30975495 [PubMed - as supplied by publisher]

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10.

Supporting medication adherence for adults with cystic fibrosis: a randomised feasibility study.

Hind D, Drabble SJ, Arden MA, Mandefield L, Waterhouse S, Maguire C, Cantrill H, Robinson L, Beever D, Scott AJ, Keating S, Hutchings M, Bradley J, Nightingale J, Allenby MI, Dewar J, Whelan P, Ainsworth J, Walters SJ, O'Cathain A, Wildman MJ.

BMC Pulm Med. 2019 Apr 11;19(1):77. doi: 10.1186/s12890-019-0834-6.

PMID: 30975206 [PubMed - in process]

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11.

Derivation of adult canine intestinal organoids for translational research in gastroenterology.

Chandra L, Borcherding DC, Kingsbury D, Atherly T, Ambrosini YM, Bourgois-Mochel A, Yuan W, Kimber M, Qi Y, Wang Q, Wannemuehler M, Ellinwood NM, Snella E, Martin M, Skala M, Meyerholz D, Estes M, Fernandez-Zapico ME, Jergens AE, Mochel JP, Allenspach K.

BMC Biol. 2019 Apr 11;17(1):33. doi: 10.1186/s12915-019-0652-6.

PMID: 30975131 [PubMed - in process]

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12.

Use of ivacaftor in late diagnosed cystic fibrosis monozygotic twins heterozygous for F508del and R117H-7T - a case report.

Welsner M, Straßburg S, Taube C, Sutharsan S.

BMC Pulm Med. 2019 Apr 11;19(1):76. doi: 10.1186/s12890-019-0840-8.

PMID: 30975115 [PubMed - in process]

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13.

An update on admissions of cystic fibrosis children in the United States based on national databases.

Ramphul K, Mejias SG, Joynauth J.

Hosp Pract (1995). 2019 Apr 11. doi: 10.1080/21548331.2019.1607351. [Epub ahead of print] No abstract available.

PMID: 30975000 [PubMed - as supplied by publisher]

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14.

CADTH Canadian Drug Expert Committee Recommendation: Lumacaftor/Ivacaftor (Orkambi — Vertex Pharmaceuticals (Canada) Incorporated): Indication: Cystic fibrosis, F508del-cystic fibrosis transmembrane conductance regulator gene mutation in patients aged six years and older [Internet].

Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2018 Oct. No abstract available.

PMID: 30973690 [PubMed] Free Books & Documents

 

15.

Uterine endometrial cytology, biopsy, bacteriology, and serum C-reactive protein in clinically healthy diestrus bitches.

Praderio RG, García Mitacek MC, Núñez Favre R, Rearte R, de la Sota RL, Stornelli MA.

Theriogenology. 2019 Apr 2;131:153-161. doi: 10.1016/j.theriogenology.2019.03.039. [Epub ahead of print]

PMID: 30974392 [PubMed - as supplied by publisher]

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16.

The Clinical Features of Bronchiectasis Associated with Alpha-1 Antitrypsin Deficiency, Common Variable Immunodeficiency and Primary Ciliary Dyskinesia--Results from the U.S. Bronchiectasis Research Registry.

Eden E, Choate R, Barker A, Addrizzo-Harris D, Aksamit TR, Daley CL, Daniels MLA, DiMango A, Fennelly K, Griffith DE, Johnson MM, Knowles MR, Metersky ML, Noone PG, O'Donnell AE, Olivier KN, Salathe MA, Schmid A, Thomashow B, Tino G, Turino GM, Winthrop KL.

Chronic Obstr Pulm Dis. 2019 Apr 9;6(2). doi: 10.15326/jcopdf.6.2.2018.0156. [Epub ahead of print]

PMID: 30974050 [PubMed - as supplied by publisher] Free Article

Similar articles

 

17.

XBP1S Regulates MUC5B in a Promoter Variant-Dependent Pathway in IPF Airway Epithelia.

Chen G, Ribeiro CMP, Sun L, Okuda K, Kato T, Gilmore RC, Martino MB, Dang H, Abzhanova A, Lin JM, Hull-Ryde EA, Volmer AS, Randell SH, Livraghi-Butrico A, Deng Y, Scherer PE, Stripp BR, O'Neal WK, Boucher RC.

Am J Respir Crit Care Med. 2019 Apr 11. doi: 10.1164/rccm.201810-1972OC. [Epub ahead of print]

PMID: 30973754 [PubMed - as supplied by publisher]

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18.

Optimizing Estimated Glomerular Filtration Rate to Support Adult to Pediatric Pharmacokinetic Bridging Studies in Patients with Cystic Fibrosis.

Crass RL, Pai MP.

Clin Pharmacokinet. 2019 Apr 10. doi: 10.1007/s40262-019-00761-5. [Epub ahead of print]

PMID: 30972695 [PubMed - as supplied by publisher]

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19.

Nebulised lipid-polymer hybrid nanoparticles for the delivery of a therapeutic anti-inflammatory microRNA to bronchial epithelial cells.

Vencken S, Foged C, Ramsey JM, Sweeney L, Cryan SA, MacLoughlin RJ, Greene CM.

ERJ Open Res. 2019 Apr 8;5(2). pii: 00161-2018. doi: 10.1183/23120541.00161-2018. eCollection 2019 Apr.

PMID: 30972350 [PubMed]

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20.

Targeting <i>Aspergillus fumigatus</i> Crf Transglycosylases With Neutralizing Antibody Is Relevant but Not Sufficient to Erase Fungal Burden in a Neutropenic Rat Model.

Chauvin D, Hust M, Schütte M, Chesnay A, Parent C, Moreira GMSG, Arroyo J, Sanz AB, Pugnière M, Martineau P, Chandenier J, Heuzé-Vourc'h N, Desoubeaux G.

Front Microbiol. 2019 Mar 26;10:600. doi: 10.3389/fmicb.2019.00600. eCollection 2019.

PMID: 30972049 [PubMed] Free Article

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21.

<i>Streptococcus gordonii</i> programs epithelial cells to resist ZEB2 induction by <i>Porphyromonas gingivalis</i>.

Ohshima J, Wang Q, Fitzsimonds ZR, Miller DP, Sztukowska MN, Jung YJ, Hayashi M, Whiteley M, Lamont RJ.

Proc Natl Acad Sci U S A. 2019 Apr 10. pii: 201900101. doi: 10.1073/pnas.1900101116. [Epub ahead of print]

PMID: 30971493 [PubMed - as supplied by publisher]

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22.

Differential thermostability and response to cystic fibrosis transmembrane conductance regulator (CFTR) potentiators of human and mouse F508del-CFTR.

Bose SJ, Bijvelds MJC, Wang Y, Liu J, Cai Z, Bot AGM, de Jonge HR, Sheppard DN.

Am J Physiol Lung Cell Mol Physiol. 2019 Apr 10. doi: 10.1152/ajplung.00034.2019. [Epub ahead of print]

PMID: 30969810 [PubMed - as supplied by publisher]

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23.

Multiprobe Nuclear Imaging of the Cystic Fibrosis Lung as a Biomarker of Therapeutic Effect.

Corcoran TE, Huber AS, Myerburg MM, Weiner DJ, Locke LW, Lacy RT, Weber L, Czachowski MR, Johnston DJ, Muthukrishnan A, Lennox AT, Pilewski JM.

J Aerosol Med Pulm Drug Deliv. 2019 Apr 10. doi: 10.1089/jamp.2018.1491. [Epub ahead of print]

PMID: 30969149 [PubMed - as supplied by publisher]

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24.

Fibroadhesive scarring of grafted collagen scaffolds interferes with implant-host neural tissue integration and bridging in experimental spinal cord injury.

Altinova H, Hammes S, Palm M, Gerardo-Nava J, Achenbach P, Deumens R, Hermans E, Führmann T, Boecker A, van Neerven SGA, Bozkurt A, Weis J, Brook GA.

Regen Biomater. 2019 Mar;6(2):75-87. doi: 10.1093/rb/rbz006. Epub 2019 Feb 4.

PMID: 30967962 [PubMed] Free PMC Article

Similar articles

 

25.

Antibacterial Properties and Efficacy of a Novel SPLUNC1-Derived Antimicrobial Peptide, α4-Short, in a Murine Model of Respiratory Infection.

Jiang S, Deslouches B, Chen C, Di ME, Di YP.

MBio. 2019 Apr 9;10(2). pii: e00226-19. doi: 10.1128/mBio.00226-19.

PMID: 30967458 [PubMed - in process] Free Article

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26.

Is it cystic fibrosis? The challenges of diagnosing cystic fibrosis.

Simmonds NJ.

Paediatr Respir Rev. 2019 Feb 28. pii: S1526-0542(19)30018-1. doi: 10.1016/j.prrv.2019.02.004. [Epub ahead of print] Review.

PMID: 30967347 [PubMed - as supplied by publisher]

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27.

Which pathogens should we worry about?

Jones AM.

Paediatr Respir Rev. 2019 Mar 1. pii: S1526-0542(19)30021-1. doi: 10.1016/j.prrv.2019.02.007. [Epub ahead of print] Review.

PMID: 30967346 [PubMed - as supplied by publisher]

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28.

FGF10 is an essential regulator of tracheal submucosal gland morphogenesis.

May AJ, Teshima THN, Noble A, Tucker AS.

Dev Biol. 2019 Apr 6. pii: S0012-1606(19)30011-9. doi: 10.1016/j.ydbio.2019.03.017. [Epub ahead of print]

PMID: 30965042 [PubMed - as supplied by publisher]

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29.

Microbial Metabolites in Cystic Fibrosis: a Target for Future Therapy?

Widder S, Knapp S.

Am J Respir Cell Mol Biol. 2019 Apr 9. doi: 10.1165/rcmb.2019-0081ED. [Epub ahead of print] No abstract available.

PMID: 30965015 [PubMed - as supplied by publisher]

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30.

Cystic fibrosis and insulin therapy: a reality check.

Warren RE.

Diabet Med. 2019 Apr 9. doi: 10.1111/dme.13959. [Epub ahead of print]

PMID: 30964946 [PubMed - as supplied by publisher]

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31.

CFTR and FOXO1 gene expression are reduced and high mobility group box 1 (HMGB1) is increased in the ovaries and serum of women with polycystic ovarian syndrome.

Cirillo F, Catellani C, Sartori C, Lazzeroni P, Morini D, Nicoli A, Giorgi-Rossi P, Amarri S, La Sala GB, Street ME.

Gynecol Endocrinol. 2019 Apr 9:1-5. doi: 10.1080/09513590.2019.1599349. [Epub ahead of print]

PMID: 30964354 [PubMed - as supplied by publisher]

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32.

Detection of pyocyanin using a new biodegradable surface enhanced Raman spectroscopy (SERS) biosensor fabricated using gold coated zein nanostructures further decorated with gold nanoparticles.

Jia F, Barber EA, Turasan H, Seo S, Dai R, Liu GL, Li X, Bhunia AK, Kokini JL.

J Agric Food Chem. 2019 Apr 9. doi: 10.1021/acs.jafc.8b07317. [Epub ahead of print]

PMID: 30964288 [PubMed - as supplied by publisher]

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33.

Relevance of heterokaryosis for adaptation and azole-resistance development in Aspergillus fumigatus.

Zhang J, Snelders EE, Zwaan BJ, Schoustra SE, Kuijper EJ, Arendrup MC, Melchers WJG, Verweij PE, Debets AJM.

Proc Biol Sci. 2019 Feb 13;286(1896):20182886. doi: 10.1098/rspb.2018.2886.

PMID: 30963936 [PubMed - in process]

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34.

Mucus and mucins in diseases of the intestinal and respiratory tracts.

Hansson GC.

J Intern Med. 2019 Apr 8. doi: 10.1111/joim.12910. [Epub ahead of print]

PMID: 30963635 [PubMed - as supplied by publisher]

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35.

Malnutrition in Children With Chronic Disease.

Larson-Nath C, Goday P.

Nutr Clin Pract. 2019 Apr 8. doi: 10.1002/ncp.10274. [Epub ahead of print] Review.

PMID: 30963628 [PubMed - as supplied by publisher]

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36.

Distal intestinal obstructive syndrome (DIOS): a gastrointestinal complication of cystic fibrosis in adults.

Mavilia M.

Clin J Gastroenterol. 2019 Apr 8. doi: 10.1007/s12328-019-00979-7. [Epub ahead of print]

PMID: 30963407 [PubMed - as supplied by publisher]

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37.

Polarized AAVR expression determines infectivity by AAV gene therapy vectors.

Hamilton BA, Li X, Pezzulo AA, Abou Alaiwa MH, Zabner J.

Gene Ther. 2019 Apr 8. doi: 10.1038/s41434-019-0078-3. [Epub ahead of print]

PMID: 30962536 [PubMed - as supplied by publisher]

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38.

<i>Burkholderia cepacia</i> complex contact-dependent growth inhibition systems mediate interbacterial competition.

Myers-Morales T, Oates AE, Byrd MS, Garcia EC.

J Bacteriol. 2019 Apr 8. pii: JB.00012-19. doi: 10.1128/JB.00012-19. [Epub ahead of print]

PMID: 30962350 [PubMed - as supplied by publisher]

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39.

Implications of fatherhood in cystic fibrosis.

Bianco B, Horsley A, Brennan A.

Paediatr Respir Rev. 2019 Mar 16. pii: S1526-0542(19)30022-3. doi: 10.1016/j.prrv.2019.02.008. [Epub ahead of print] Review.

PMID: 30962151 [PubMed - as supplied by publisher]

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40.

Cystic fibrosis: Diagnosis and management - NICE guideline 78.

Walshaw MJ.

Paediatr Respir Rev. 2019 Feb 28. pii: S1526-0542(19)30020-X. doi: 10.1016/j.prrv.2019.02.006. [Epub ahead of print] Review.

PMID: 30962150 [PubMed - as supplied by publisher]

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41.

Health-related quality of life and stress-related post-transplant trajectories of lung transplant recipients: a three-year follow-up of the Swiss Transplant Cohort Study

Bleisch B, Schuurmans MM, Klaghofer R, Benden C, Seiler A, Jenewein J.

Swiss Med Wkly. 2019 Feb 24;149(07-08). doi: 10.4414/smw.2019.20019. eCollection 2019 Feb 11.

PMID: 30961347 [PubMed - in process] Free Article

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42.

Surgical Management of Chronic Rhinosinusitis in Cystic Fibrosis.

Zheng Z, Safi C, Gudis DA.

Med Sci (Basel). 2019 Apr 7;7(4). pii: E57. doi: 10.3390/medsci7040057. Review.

PMID: 30959944 [PubMed] Free Article

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43.

Proline-Glycine-Proline Peptides Are Critical in the Development of Smoke-Induced Emphysema.

Abdul Roda M, Xu X, Abdalla TH, Sadik M, Szul T, Bratcher PE, Viera L, Solomon GM, Wells JM, McNicholas CM, Redegeld FA, Folkerts G, Blalock JE, Gaggar A.

Am J Respir Cell Mol Biol. 2019 Apr 8. doi: 10.1165/rcmb.2018-0216OC. [Epub ahead of print]

PMID: 30958968 [PubMed - as supplied by publisher]

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44.

[CURRENT APPROACHES TO PREVENTION OF BLEEDINGS, ASSOCIATED WITH VITAMIN K DEFICIENCY IN NEWBORNS AND INFANTS].

Kiselova M.

Georgian Med News. 2019 Feb;(287):45-50. Russian.

PMID: 30958287 [PubMed - in process]

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45.

SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens.

Wu YN, Chen KC, Wu CC, Lin YH, Chiang HS.

Biomed Res Int. 2019 Mar 10;2019:3562719. doi: 10.1155/2019/3562719. eCollection 2019.

PMID: 30956978 [PubMed - in process] Free PMC Article

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46.

Disseminated <i>Scedosporium apiospermum</i> central nervous system infection after lung transplantation: A case report with successful recovery.

Paajanen J, Halme M, Palomäki M, Anttila VJ.

Med Mycol Case Rep. 2019 Mar 16;24:37-40. doi: 10.1016/j.mmcr.2019.03.003. eCollection 2019 Jun.

PMID: 30956943 [PubMed] Free PMC Article

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47.

<i>Porphyromonas</i>, a potential predictive biomarker of <i>Pseudomonas aeruginosa</i> pulmonary infection in cystic fibrosis.

Keravec M, Mounier J, Guilloux CA, Fangous MS, Mondot S, Vallet S, Gouriou S, Le Berre R, Rault G, Férec C, Barbier G, Lepage P, Héry-Arnaud G.

BMJ Open Respir Res. 2019 Mar 12;6(1):e000374. doi: 10.1136/bmjresp-2018-000374. eCollection 2019.

PMID: 30956802 [PubMed] Free PMC Article

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48.

Cystic Fibrosis Transmembrane Conductance Regulator Genotype, Not Circulating Catecholamines, Influences Cardiovascular Function in Patients with Cystic Fibrosis.

Bisch AL, Wheatley CM, Baker SE, Peitzman ER, Van Iterson EH, Laguna TA, Morgan WJ, Snyder EM.

Clin Med Insights Circ Respir Pulm Med. 2019 Mar 29;13:1179548419835788. doi: 10.1177/1179548419835788. eCollection 2019.

PMID: 30956528 [PubMed] Free PMC Article

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49.

Cytomegalovirus - an unrecognised potential contributor to cystic fibrosis disease progression?

Parkins MD, Ramos KJ, Goss CH, Somayaji R.

Eur Respir J. 2019 Apr 7. pii: 1801727. doi: 10.1183/13993003.01727-2018. [Epub ahead of print]

PMID: 30956206 [PubMed - as supplied by publisher]

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50.

Newborn screening for cystic fibrosis: Is there benefit for everyone?

Course CW, Hanks R.

Paediatr Respir Rev. 2019 Feb 28. pii: S1526-0542(19)30017-X. doi: 10.1016/j.prrv.2019.02.003. [Epub ahead of print] Review.

PMID: 30956155 [PubMed - as supplied by publisher]

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51.  Assessment of endothelial function is reproducible in patients with cystic fibrosis.

        Derella CC, Lee N, Crandall R, Blackburn M, Looney J, Mangieri A, Rodriguez-Miguelez P, Tucker MA, Harris RA.

        J Cyst Fibros. 2019 Apr 4. pii: S1569-1993(19)30062-1. doi: 10.1016/j.jcf.2019.03.011. [Epub ahead of print]

        PMID: 30956017

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52. Lectin activity of Pseudomonas aeruginosa vaccine candidates PSE17-1, PSE41-5 and PSE54.

        Day CJ, Hartley-Tassell LE, Seib KL, Tiralongo J, Bovin N, Savino S, Masignani V, Jennings MP.

        Biochem Biophys Res Commun. 2019 Apr 3. pii: S0006-291X(19)30481-4. doi: 10.1016/j.bbrc.2019.03.092. [Epub ahead of print]

        PMID: 30954224

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53. Asymptomatic catheter-related venous thrombosis in a child with cystic fibrosis: When to treat?

       Schapkaitz E, Weil R, White D, Klugman S.

       J Vasc Nurs. 2019 Mar;37(1):43-45. doi: 10.1016/j.jvn.2018.09.001. Epub 2018 Nov 7.

      PMID: 30954197

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54. A specific combined long-chain polyunsaturated fatty acid supplementation reverses fatty acid profile alterations in a mouse model of chronic asthma.

       Fussbroich D, Zimmermann K, Göpel A, Eickmeier O, Trischler J, Zielen S, Schubert R, Beermann C.

       Lipids Health Dis. 2019 Jan 18;18(1):16. doi: 10.1186/s12944-018-0947-6.

       PMID:  30658644

       Free PMC Article

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55.  Preclinical therapeutic efficacy of the ciprofloxacin-eluting sinus stent for Pseudomonas aeruginosa sinusitis.

        Cho DY, Lim DJ, Mackey C, Skinner D, Weeks C, Gill GS, Hergenrother RW, Swords WE, Woodworth BA.

        Int Forum Allergy Rhinol. 2018 Apr;8(4):482-489. doi: 10.1002/alr.22081. Epub 2018 Jan 15.

        PMID: 29334430

        Free PMC Article

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Associació Catalana de Fibrosi Quística

Passeig Reina Elisenda de Montcada 5

08034 Barcelona

Tel. i fax: 934272228

www.fibrosiquistica.org

fqcatalana@fibrosiquisticaorg

 

 

 

 

 

 

ASSOCIACIÓ CATALANA DE FIBROSI QUÍSTICA

23/03/2019

Citas bibliográficas entradas en PubMed desde 16/03/2019

 Criterio de filtrado "cystic fibrosis"

 

Items 1 - 50 of 51

 

1.

Methicillin-resistant Staphylococcus aureus eradication in cystic fibrosis patients: A randomized multicenter study.

Dolce D, Neri S, Grisotto L, Campana S, Ravenni N, Miselli F, Camera E, Zavataro L, Braggion C, Fiscarelli EV, Lucidi V, Cariani L, Girelli D, Faelli N, Colombo C, Lucanto C, Lombardo M, Magazzù G, Tosco A, Raia V, Manara S, Pasolli E, Armanini F, Segata N, Biggeri A, Taccetti G.

PLoS One. 2019 Mar 22;14(3):e0213497. doi: 10.1371/journal.pone.0213497. eCollection 2019.

PMID: 30901344 [PubMed - in process]

 

2.

Tailored nanocarriers for the pulmonary delivery of levofloxacin against Pseudomonas aeruginosa: a comparative study.

Derbali RM, Aoun V, Moussa G, Frei G, F Tehrani S, Campos Del'Orto J, Hildgen P, Roullin VG, Leblond Chain J.

Mol Pharm. 2019 Mar 22. doi: 10.1021/acs.molpharmaceut.8b01256. [Epub ahead of print]

PMID: 30900903 [PubMed - as supplied by publisher]

 

3.

Pulmonary Acinus: Understanding the Computed Tomography Findings from an Acinar Perspective.

Hochhegger B, Langer FW, Irion K, Souza A, Moreira J, Baldisserotto M, Pallaoro Y, Muller E, Medeiros TM, Altmayer S, Marchiori E.

Lung. 2019 Mar 21. doi: 10.1007/s00408-019-00214-7. [Epub ahead of print] Review.

PMID: 30900014 [PubMed - as supplied by publisher]

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4.

Isolation of <i>Aggregatibacter aphrophilus</i> from bronchoalveolar lavage in a paediatric patient presenting with haemoptysis.

Patas K, Douros K, Priftis KN, Ioannidis A, Nikolaou C, Chatzipanagiotou S.

New Microbes New Infect. 2019 Feb 7;29:100509. doi: 10.1016/j.nmni.2019.01.005. eCollection 2019 May.

PMID: 30899518 [PubMed]

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5.

The gliadin-CFTR connection: new perspectives for the treatment of celiac disease.

Maiuri L, Villella VR, Raia V, Kroemer G.

Ital J Pediatr. 2019 Mar 21;45(1):40. doi: 10.1186/s13052-019-0627-9.

PMID: 30898172 [PubMed - in process]

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6.

Spectrum of CFTR mutations in Chechen cystic fibrosis patients: high frequency of c.1545_1546delTA (p.Tyr515X; 1677delTA) and c.274G&gt;A (p.Glu92Lys, E92K) mutations in North Caucasus.

Petrova NV, Kashirskaya NY, Saydaeva DK, Polyakov AV, Adyan TA, Simonova OI, Gorinova YV, Kondratyeva EI, Sherman VD, Novoselova OG, Vasilyeva TA, Marakhonov AV, Macek M Jr, Ginter EK, Zinchenko RA.

BMC Med Genet. 2019 Mar 21;20(1):44. doi: 10.1186/s12881-019-0785-z.

PMID: 30898088 [PubMed - in process]

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7.

Brevenal, a Marine Natural Product, is Anti-Inflammatory and an Immunomodulator of Macrophage and Lung Epithelial Cells.

Keeler DM, Grandal MK, McCall JR.

Mar Drugs. 2019 Mar 20;17(3). pii: E184. doi: 10.3390/md17030184.

PMID: 30897777 [PubMed - in process]

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8.

Nutritional Treatment of a Young Infant with Cystic Fibrosis Presenting with Severe Kwashiorkor Dermatosis.

Sandy NS, Nogueira RJN.

J Trop Pediatr. 2019 Mar 20. pii: fmz008. doi: 10.1093/tropej/fmz008. [Epub ahead of print]

PMID: 30897613 [PubMed - as supplied by publisher]

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9.

Tetrafunctional Block Copolymers Promote Lung Gene Transfer in Newborn Piglets.

Caballero I, Riou M, Hacquin O, Chevaleyre C, Barc C, Pezant J, Pinard A, Fassy J, Rezzonico R, Mari B, Heuzé-Vourc'h N, Pitard B, Vassaux G.

Mol Ther Nucleic Acids. 2019 Feb 26;16:186-193. doi: 10.1016/j.omtn.2019.02.016. [Epub ahead of print]

PMID: 30897407 [PubMed - as supplied by publisher] Free Article

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10.

Pharmacotherapeutic strategies for treating bronchiectasis in pediatric patients.

Lee E, Hong SJ.

Expert Opin Pharmacother. 2019 Mar 21:1-12. doi: 10.1080/14656566.2019.1589453. [Epub ahead of print]

PMID: 30897021 [PubMed - as supplied by publisher]

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11.

Mice with a Deletion of Rsph1 Exhibit a Low Level of Mucociliary Clearance and Develop a PCD Phenotype.

Yin W, Livraghi-Butrico A, Sears PR, Rogers TD, Burns KA, Grubb BR, Ostrowski LE.

Am J Respir Cell Mol Biol. 2019 Mar 21. doi: 10.1165/rcmb.2017-0387OC. [Epub ahead of print]

PMID: 30896965 [PubMed - as supplied by publisher]

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12.

Experience of Using a Semielemental Formula for Home Enteral Nutrition in Children: A Multicenter Cross-sectional Study.

Leonard M, Caldari D, Mas E, Lambe C, Comte A, Ley D, Peretti N, Borderon C, Marinier E, Coste ME, Lamireau T, Rubio A, Turquet A, Dubern B, Dabadie A, Gautry J, Kyheng M, Guimber D, Gottrand F.

J Pediatr Gastroenterol Nutr. 2019 Apr;68(4):585-590. doi: 10.1097/MPG.0000000000002236.

PMID: 30896609 [PubMed - in process]

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13.

Cutaneous small-vessel vasculitis associated with paediatric ulcerative colitis: A case study and literature review.

Romano C, Valenti S, Pidone C, Spina M, Caruso RA, Gallizzi R, Dipasquale V.

J Paediatr Child Health. 2019 Mar 20. doi: 10.1111/jpc.14440. [Epub ahead of print] No abstract available.

PMID: 30895688 [PubMed - as supplied by publisher]

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14.

<i>In vitro</i> Interactions of <i>Pseudomonas aeruginosa</i> With <i>Scedosporium</i> Species Frequently Associated With Cystic Fibrosis.

Homa M, Sándor A, Tóth E, Szebenyi C, Nagy G, Vágvölgyi C, Papp T.

Front Microbiol. 2019 Mar 6;10:441. doi: 10.3389/fmicb.2019.00441. eCollection 2019.

PMID: 30894846 [PubMed] Free Article

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15.

Glucose tolerance in Canadian and French cystic fibrosis adult patients.

Reynaud Q, Boudreau V, Touzet S, Desjardins K, Bourdy SP, Blond E, Berthiaume Y, Rabasa-Lhoret R, Durieu I.

Sci Rep. 2019 Mar 18;9(1):4763. doi: 10.1038/s41598-019-40592-9.

PMID: 30894563 [PubMed - in process] Free Article

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16.

Rapid cell division of Staphylococcus aureus during colonization of the human nose.

Szafrańska AK, Junker V, Steglich M, Nübel U.

BMC Genomics. 2019 Mar 20;20(1):229. doi: 10.1186/s12864-019-5604-6.

PMID: 30894139 [PubMed - in process] Free Article

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17.

Cell-Selective Regulation of CFTR Gene Expression: Relevance to Gene Editing Therapeutics.

Swahn H, Harris A.

Genes (Basel). 2019 Mar 19;10(3). pii: E235. doi: 10.3390/genes10030235. Review.

PMID: 30893953 [PubMed] Free Article

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18.

Contribution of Anoctamins to Cell Survival and Cell Death.

Kunzelmann K, Ousingsawat J, Benedetto R, Cabrita I, Schreiber R.

Cancers (Basel). 2019 Mar 19;11(3). pii: E382. doi: 10.3390/cancers11030382. Review.

PMID: 30893776 [PubMed] Free Article

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19.

Successful ceftazidime-avibactam treatment of post-surgery Burkholderia multivorans genomovar II bacteremia and brain abscesses in a young lung transplanted woman with cystic fibrosis.

Daccò V, Claut L, Piconi S, Castellazzi L, Garbarino F, Teri A, Colombo C.

Transpl Infect Dis. 2019 Mar 20:e13082. doi: 10.1111/tid.13082. [Epub ahead of print]

PMID: 30892778 [PubMed - as supplied by publisher]

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20.

Infection prevention and control in cystic fibrosis: a systematic review of interventions.

Rowbotham NJ, Palser SC, Smith SJ, Smyth AR.

Expert Rev Respir Med. 2019 Mar 20. doi: 10.1080/17476348.2019.1595594. [Epub ahead of print]

PMID: 30892097 [PubMed - as supplied by publisher]

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21.

Acetyl-CoA carboxylase inhibition regulates microtubule dynamics and intracellular transport in cystic fibrosis epithelial cells.

Rymut SM, Lu B, Perez A, Corey DA, Lamb K, Cotton CU, Kelley TJ.

Am J Physiol Lung Cell Mol Physiol. 2019 Mar 20. doi: 10.1152/ajplung.00369.2018. [Epub ahead of print]

PMID: 30892081 [PubMed - as supplied by publisher]

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22.

<i>Pseudomonas aeruginosa</i> in cystic fibrosis: A chronic cheater.

Waters CM, Goldberg JB.

Proc Natl Acad Sci U S A. 2019 Mar 19. pii: 201902734. doi: 10.1073/pnas.1902734116. [Epub ahead of print] No abstract available.

PMID: 30890646 [PubMed - as supplied by publisher]

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23.

Persistent Adherence to Airway Clearance Therapy in Adults With Cystic Fibrosis.

Sherman AC, Simonton-Atchley S, Campbell D, Reddy RM, O'Brien CE, Guinee B, Wagner LD, Anderson PJ.

Respir Care. 2019 Mar 19. pii: respcare.06500. doi: 10.4187/respcare.06500. [Epub ahead of print]

PMID: 30890632 [PubMed - as supplied by publisher]

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24.

Higher Levels of Education Are Associated With Full-Time Work in Adults With Cystic Fibrosis.

Lian R, Cavalheri V, Wood J, Jenkins S, Straker LM, Hill K.

Respir Care. 2019 Mar 19. pii: respcare.06607. doi: 10.4187/respcare.06607. [Epub ahead of print]

PMID: 30890629 [PubMed - as supplied by publisher]

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25.

Choline Supplementation in Cystic Fibrosis-The Metabolic and Clinical Impact.

Bernhard W, Lange R, Graepler-Mainka U, Engel C, Machann J, Hund V, Shunova A, Hector A, Riethmüller J.

Nutrients. 2019 Mar 18;11(3). pii: E656. doi: 10.3390/nu11030656.

PMID: 30889905 [PubMed - in process] Free Article

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26.

Higher Plasma Endothelial Markers in Adults with Cystic Fibrosis Compared to Healthy Age Matched Controls.

Bhatraju PK, Hisert KB, Aitken ML, Goss CH, Liles WC, Altemeier WA.

Ann Am Thorac Soc. 2019 Mar 19. doi: 10.1513/AnnalsATS.201812-844RL. [Epub ahead of print] No abstract available.

PMID: 30889361 [PubMed - as supplied by publisher]

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27.

Correlating CFTR Function with Clinical Features to Inform Precision Treatment of Cystic Fibrosis.

McCague AF, Raraigh KS, Pellicore MJ, Davis-Marcisak EF, Evans TA, Han ST, Lu Z, Joynt AT, Sharma N, Castellani C, Collaco JM, Corey M, Lewis MH, Penland CM, Rommens JM, Stephenson AL, Sosnay PR, Cutting GR.

Am J Respir Crit Care Med. 2019 Mar 19. doi: 10.1164/rccm.201901-0145OC. [Epub ahead of print]

PMID: 30888834 [PubMed - as supplied by publisher]

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28.

Exophiala dermatitidis: key issues of an opportunistic fungal pathogen.

Kirchhoff L, Olsowski M, Rath PM, Steinmann J.

Virulence. 2019 Mar 19. doi: 10.1080/21505594.2019.1596504. [Epub ahead of print]

PMID: 30887863 [PubMed - as supplied by publisher]

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29.

Linkage of the CF foundation patient registry with the pediatric health information system database.

Cogen JD, Hall M, Loeffler DR, Gove N, Onchiri F, Sawicki GS, Fink AK.

Pediatr Pulmonol. 2019 Mar 18. doi: 10.1002/ppul.24272. [Epub ahead of print]

PMID: 30887732 [PubMed - as supplied by publisher]

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30.

Identifying pediatric lung disease: A comparison of forced oscillation technique outcomes.

Evans DJ, Schultz A, Verheggen M, Hall GL, Simpson SJ.

Pediatr Pulmonol . 2019 Mar 18. doi: 10.1002/ppul.24286. [Epub ahead of print]

PMID: 30887730 [PubMed - as supplied by publisher]

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31.

Validity and Reliability of a Novel Multimodal Questionnaire for the Assessment of Abdominal Symptoms in People with Cystic Fibrosis (CFAbd-Score).

Jaudszus A, Zeman E, Jans T, Pfeifer E, Tabori H, Arnold C, Michl RK, Lorenz M, Beiersdorf N, Mainz JG.

Patient. 2019 Mar 18. doi: 10.1007/s40271-019-00361-2. [Epub ahead of print]

PMID: 30887269 [PubMed - as supplied by publisher]

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32.

Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis.

Ashkenazi M, Nathan N, Sarouk I, Aluma BEB, Dagan A, Bezalel Y, Keler S, Vilozni D, Efrati O.

Lung. 2019 Mar 18. doi: 10.1007/s00408-019-00218-3. [Epub ahead of print]

PMID: 30887107 [PubMed - as supplied by publisher]

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33.

The Yin and Yang of <i>Streptococcus</i> Lung Infections in Cystic Fibrosis: A Model for Studying Polymicrobial Interactions.

Scott JE, O'Toole GA.

J Bacteriol. 2019 Mar 18. pii: JB.00115-19. doi: 10.1128/JB.00115-19. [Epub ahead of print] Review.

PMID: 30885933 [PubMed - as supplied by publisher]

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34.

Diagnostic accuracy of MRI with MRCP and B-Mode-sonography with elastography of the pancreas in patients with cystic fibrosis: a point-to-point comparison.

Kloth C, Fabricius D, Wendlik I, Schmidt SA, Pfahler M, Lormes E, Beer M, Kratzer W, Schmidberger J.

BMC Res Notes. 2019 Mar 18;12(1):150. doi: 10.1186/s13104-019-4193-4.

PMID: 30885270 [PubMed - in process] Free Article

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35.

Computed Tomography Description of the Uncinate Process Angulation in Patients With Cystic Fibrosis and Comparison With Primary Ciliary Dyskinesia, Nasal Polyposis, and Controls.

Hervochon R, Teissier N, Blondeau JR, Remus N, Bassinet L, Canoui-Poitrine F, Van Den Abbeele T, Prulière-Escabasse V.

Ear Nose Throat J. 2019 Feb;98(2):89-93. doi: 10.1177/0145561319828645. Epub 2019 Feb 7.

PMID: 30884997 [PubMed - in process]

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36.

Aerosolized agents for airway clearance in cystic fibrosis.

Southern KW, Clancy JP, Ranganathan S.

Pediatr Pulmonol. 2019 Mar 18. doi: 10.1002/ppul.24306. [Epub ahead of print]

PMID: 30884217 [PubMed - as supplied by publisher]

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37.

Pulmonary Mycobacterium abscessus complex in children with cystic fibrosis: A practical management guideline.

Andrew EC, Connell T, Robinson P, Curtis N, Massie J, Robertson C, Harrison J, Shanthikumar S, Bryant PA, Starr M, Steer A, Ranganathan S, Gwee A.

J Paediatr Child Health. 2019 Mar 18. doi: 10.1111/jpc.14427. [Epub ahead of print] Review.

PMID: 30884016 [PubMed - as supplied by publisher]

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38.

Hydroxyurea (hydroxycarbamide) for transfusion-dependent β-thalassaemia.

Ansari SH, Lassi ZS, Khowaja SM, Adil SO, Shamsi TS.

Cochrane Database Syst Rev. 2019 Mar 16;3:CD012064. doi: 10.1002/14651858.CD012064.pub2. [Epub ahead of print] Review.

PMID: 30882896 [PubMed - as supplied by publisher]

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39.

Nebulized Amikacin and Fosfomycin for Severe Pseudomonas aeruginosa Pneumonia: An Experimental Study.

Li Bassi G, Motos A, Fernandez-Barat L, Aguilera Xiol E, Chiurazzi C, Senussi T, Saco MA, Fuster C, Carbonara M, Bobi J, Amaro R, De Rosa F, Comaru T, Yang H, Ranzani OT, Marti JD, Rinaudo M, Comino Trinidad O, Rigol M, Bringué J, Ramirez J, Nicolau DP, Pelosi P, Antonelli M, Blasi F, Artigas A, Montgomery AB, Torres A.

Crit Care Med. 2019 Mar 15. doi: 10.1097/CCM.0000000000003724. [Epub ahead of print]

PMID: 30882478 [PubMed - as supplied by publisher]

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40.

Aerosol Transmission of Aspergillus fumigatus in Cystic Fibrosis Patients in the Netherlands.

Engel TGP, Erren E, Vanden Driessche KSJ, Melchers WJG, Reijers MH, Merkus P, Verweij PE.

Emerg Infect Dis. 2019 Apr;25(4):797-799. doi: 10.3201/eid2504.181110.

PMID: 30882308 [PubMed - in process] Free Article

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41.

Pore-forming small molecules offer a promising way to tackle cystic fibrosis.

Sheppard DN, Davis AP.

Nature. 2019 Mar;567(7748):315-317. doi: 10.1038/d41586-019-00781-y. No abstract available.

PMID: 30880331 [PubMed - in process]

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42.

Accuracy of Transient Elastography Data Combined With APRI in Detection and Staging of Liver Disease in Pediatric Patients With Cystic Fibrosis.

Lewindon PJ, Puertolas-Lopez MV, Ramm LE, Noble C, Pereira TN, Wixey JA, Hartel GF, Calvopina DA, Leung DH, Ramm GA.

Clin Gastroenterol Hepatol. 2019 Mar 14. pii: S1542-3565(19)30279-4. doi: 10.1016/j.cgh.2019.03.015. [Epub ahead of print]

PMID: 30880274 [PubMed - as supplied by publisher]

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43.

Effects of Lumacaftor/Ivacaftor on physical activity and exercise tolerance in three adults with cystic fibrosis.

Savi D, Schiavetto S, Simmonds NJ, Righelli D, Palange P.

J Cyst Fibros. 2019 Mar 14. pii: S1569-1993(19)30053-0. doi: 10.1016/j.jcf.2019.03.001. [Epub ahead of print]

PMID: 30879989 [PubMed - as supplied by publisher]

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44.

Caroli Disease Revisited: A Case of a Kidney Transplant Patient With Autosomal Polycystic Kidney Disease and Recurrent Episodes of Cholangitis.

Kumar A, Akselrod D, Prikis M.

Transplant Proc. 2019 Mar;51(2):541-544. doi: 10.1016/j.transproceed.2018.12.025. Epub 2019 Jan 3.

PMID: 30879585 [PubMed - in process]

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45.

Challenges and safety of beta lactam desensitization during extracorporeal membrane oxygenation.

Foer D, Marquis K, Romero N, Castells MC.

Ann Allergy Asthma Immunol. 2019 Mar 13. pii: S1081-1206(19)30184-X. doi: 10.1016/j.anai.2019.03.005. [Epub ahead of print] No abstract available.

PMID: 30878628 [PubMed - as supplied by publisher]

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46.

Posaconazole therapy in children with cystic fibrosis and Aspergillus-related lung disease.

Patel D, Popple S, Claydon A, Modha DE, Gaillard EA.

Med Mycol. 2019 Mar 16. pii: myz015. doi: 10.1093/mmy/myz015. [Epub ahead of print]

PMID: 30877757 [PubMed - as supplied by publisher]

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47.

Biochemistry of very-long-chain and long-chain ceramides in cystic fibrosis and other diseases: The importance of side chain.

Garić D, De Sanctis JB, Shah J, Dumut DC, Radzioch D.

Prog Lipid Res. 2019 Mar 12. pii: S0163-7827(19)30011-6. doi: 10.1016/j.plipres.2019.03.001. [Epub ahead of print] Review.

PMID: 30876862 [PubMed - as supplied by publisher]

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48.

Lentiviral Vectors for the Treatment and Prevention of Cystic Fibrosis Lung Disease.

Marquez Loza LI, Yuen EC, McCray PB Jr.

Genes (Basel). 2019 Mar 14;10(3). pii: E218. doi: 10.3390/genes10030218. Review.

PMID: 30875857 [PubMed] Free Article

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49.

In-vitro analysis of a novel 'add-on' silicone cuff to improve sealing properties of tracheal tubes.

Li Bassi G, Chiurazzi C, Aguilera E, Travierso C, Battaglini D, Yang M, Motos A, Yang H, Meli A, Marti D, Ranzani OT, Blasi F, Pelosi P, Chiumello D, Torres A.

Anaesthesia. 2018 Nov;73(11):1372-1381. doi: 10.1111/anae.14413.

PMID: 30298583 [PubMed - indexed for MEDLINE]

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50.

Type I interferon pathway activation in COPA syndrome.

Volpi S, Tsui J, Mariani M, Pastorino C, Caorsi R, Sacco O, Ravelli A, Shum AK, Gattorno M, Picco P.

Clin Immunol. 2018 Feb;187:33-36. doi: 10.1016/j.clim.2017.10.001. Epub 2017 Oct 10.

PMID: 29030294 [PubMed - indexed for MEDLINE]

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51. E-Liquid Autofluorescence can be used as a Marker of Vaping Deposition and Third-Hand Vape Exposure.

      Davis ES, Sassano MF, Goodell H, Tarran R.

       Sci Rep. 2017 Aug 7;7(1):7459. doi: 10.1038/s41598-017-07862-w.

       PMID: 28785072 Free PMC Article

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