PubMed Clinical Queries
From PubMed Clinical Queries
PubMed Clinical Queries is an utility offered by PubMed to search scientific literature in specific clinical research areas
Children and Adults Tai Chi Study (CF-CATS2): a randomised controlled feasibility study comparing internet-delivered with face-to-face Tai Chi lessons in cystic fibrosis. Carr SB, Ronan P, Lorenc A, Mian A, Madge SL, Robinson N. ERJ Open Res. 2018 Oct; 4(4). Epub 2018 Dec 14.
Spotlight on inhaled ciprofloxacin and its potential in the treatment of non-cystic fibrosis bronchiectasis. Chorepsima S, Kechagias KS, Kalimeris G, Triarides NA, Falagas ME. Drug Des Devel Ther. 2018; 12:4059-4066. Epub 2018 Nov 27.
Effect of ivacaftor on mucociliary clearance and clinical outcomes in cystic fibrosis patients with G551D-CFTR. Donaldson SH, Laube BL, Corcoran TE, Bhambhvani P, Zeman K, Ceppe A, Zeitlin PL, Mogayzel PJ Jr, Boyle M, Locke LW, et al. JCI Insight. 2018 Dec 20; 3(24). Epub 2018 Dec 20.
A randomized trial of vitamin D in acute-stage allergic bronchopulmonary aspergillosis complicating asthma. Dodamani MH, Muthu V, Thakur R, Pal A, Sehgal IS, Dhooria S, Aggarwal AN, Garg M, Chakrabarti A, Agarwal R. Mycoses. 2018 Dec 18; . Epub 2018 Dec 18.
Acceptability of Electronic Visits for Return of Research Results in the Mayo Clinic Biobank. Olson JE, Ryu E, Lyke KJ, Bielinski SJ, Winkler EM, Hathcock MA, Bublitz JT, Takahashi PY, Cerhan JR. Mayo Clin Proc Innov Qual Outcomes. 2018 Dec; 2(4):352-358. Epub 2018 Sep 15.
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Recombinant growth hormone therapy for cystic fibrosis in children and young adults. Thaker V, Carter B, Putman M. Cochrane Database Syst Rev. 2018 Dec 17; 12:CD008901. Epub 2018 Dec 17.
Efficacy and Safety of CFTR Corrector and Potentiator Combination Therapy in Patients with Cystic Fibrosis for the F508del-CFTR Homozygous Mutation: A Systematic Review and Meta-analysis. Wu HX, Zhu M, Xiong XF, Wei J, Zhuo KQ, Cheng DY. Adv Ther. 2018 Dec 15; . Epub 2018 Dec 15.
Vaccines for preventing invasive salmonella infections in people with sickle cell disease. Odey F, Okomo U, Oyo-Ita A. Cochrane Database Syst Rev. 2018 Dec 5; 12:CD006975. Epub 2018 Dec 5.
Pre-transplant factors associated with mortality after lung transplantation in cystic fibrosis: A systematic review and meta-analysis. Koutsokera A, Varughese RA, Sykes J, Orchanian-Cheff A, Shah PS, Chaparro C, Tullis E, Singer LG, Stephenson AL. J Cyst Fibros. 2018 Oct 25; . Epub 2018 Oct 25.
Gene therapy for sickle cell disease. Olowoyeye A, Okwundu CI. Cochrane Database Syst Rev. 2018 Nov 16; 11:CD007652. Epub 2018 Nov 16.
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Medical Genetics Topic: All Diagnosis Differential Diagnosis Clinical Description Management Genetic Counseling Molecular Genetics Genetic Testing
Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported cases. Guo X, Liu K, Liu Y, Situ Y, Tian X, Xu KF, Zhang X. Orphanet J Rare Dis. 2018 Dec 17; 13(1):224. Epub 2018 Dec 17.
A case report on filamin A gene mutation and progressive pulmonary disease in an infant: A lung tissued derived mesenchymal stem cell study. Calcaterra V, Avanzini MA, Mantelli M, Agolini E, Croce S, De Silvestri A, Re G, Collura M, Maltese A, Novelli A, et al. Medicine (Baltimore). 2018 Dec; 97(50):e13033.
Recombinant growth hormone therapy for cystic fibrosis in children and young adults. Thaker V, Carter B, Putman M. Cochrane Database Syst Rev. 2018 Dec 17; 12:CD008901. Epub 2018 Dec 17.
Comprehensive genotyping reveals novel CFTR variants in cystic fibrosis patients from the Russian Federation. Petrova NV, Marakhonov AV, Vasilyeva TA, Kashirskaya NY, Ginter EK, Kutsev SI, Zinchenko RA. Clin Genet. 2018 Dec 12; . Epub 2018 Dec 12.
Draft Genome Sequences of Two Cystic Fibrosis Strains of Stenotrophomonas maltophilia, AU30115 and AU32848. Eckstrom K, Willsey GG, LiPuma JJ, Wargo MJ. Microbiol Resour Announc. 2018 Sep; 7(11). Epub 2018 Sep 20.
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