Citations Report

Clinical Practice : Citations & Metrics Report

Articles published in Clinical Practice have been cited by esteemed scholars and scientists all around the world.

Clinical Practice has got h-index 29, which means every article in Clinical Practice has got 29 average citations.

Following are the list of articles that have cited the articles published in Clinical Practice.

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• Syed SA, Whelan FJ, Waddell B, Rabin HR, Parkins MD, et al. 2016. Reemergence of Lower-Airway Microbiota in Lung Transplant Patients with Cystic Fibrosis. Annals of the American Thoracic Society, 13(12), pp.2132-2142.

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• Zemanick ET and Harris JK, 2013. The Human Airway Microbiome. The Human Microbiota: How Microbial Communities Affect Health and Disease, pp.119-134.

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• Liu KE, Love AC and Travisano M, 2016. 5 How Cancer Spreads. Philosophy of Molecular Medicine: Foundational Issues in Research and Practice.

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• Waite RD, Qureshi MR and Whiley RA, 2017. Modulation of behaviour and virulence of a high alginate expressing Pseudomonas aeruginosa strain from cystic fibrosis by oral commensal bacterium Streptococcus anginosus. PloS one, 12(3), p.e0173741.

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• Waite RD, Qureshi MR and Whiley RA, 2017. Modulation of behaviour and virulence of a high alginate expressing Pseudomonas aeruginosa strain from cystic fibrosis by oral commensal bacterium Streptococcus anginosus. PloS one, 12(3), p.e0173741.

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• Lacroix AMG, 2014. Investigation of Competence Heterogeneity in Streptococcus Milleri Group Clinical Isolates (Doctoral dissertation).

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• Schlam D, 2016. Regulation of Phagocyte Immunity by Lipid Signals (Doctoral dissertation, University of Toronto (Canada)).

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• Fang J, 2014. Study of Specialized Metabolites Produced by Pseudomonas aeruginosa Using Mass Spectrometry.

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• Denman CC, 2013. From Osmolytes to Diabetes: the Impact of Sugars and Sugar Alcohols on the Cystic Fibrosis Pathogen, Burkholderia multivorans.

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• Barott KL, 2012. Competition between coral and algal holobionts.

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• Zhao Y, 2014. Pseudomonas aeruginosa type III secretion system: regulation and potential role in interspecies interaction (Doctoral dissertation, University of Manitoba).

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• Kirkup Jr BC, 2014. Counterinsurgency Doctrine Applied to Infectious Disease (Doctoral dissertation, School of Medicine, Uniformed Services University of the Health Sciences).

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• Nolan LM, 2014. The role of small molecule signalling in biofilm migration of Pseudomonas aeruginosa (Doctoral dissertation).

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• Lopes SP, Carvalho DT, Pereira MO and Azevedo NF, 2017. Discriminating typical and atypical cystic fibrosis‐related bacteria by multiplex PNA‐FISH. Biotechnology and Bioengineering, 114(2), pp.355-367.

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• Bhagirath AY, Li Y, Somayajula D, Dadashi M, Badr S, et al. 2016. Cystic fibrosis lung environment and Pseudomonas aeruginosa infection. BMC Pulmonary Medicine, 16(1), p.174.

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• Singh P, 2011. Structural and Functional Characterization of Bacterial Secretion Systems Using Mass Spectrometry. University of Washington.

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• Halverson TWR, 2013. The role of extracellular DNA in neutrophil extracellular traps (Doctoral dissertation, University of Calgary).

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• Sato Y, 2012. Ecology and microbiology of black band disease: new insights into the etiology of an old coral disease (Doctoral dissertation, James Cook University).

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• Mougous J, University Of Washington, 2010. Toxin-Immunity System. U.S. Patent Application 13/516,158.

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• Hoppe JE, Harris JK and Zemanick ET, 2016. Assessing the Airway Microbiota in Cystic Fibrosis. Clinical Microbiology Newsletter, 38(22), pp.179-184.

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• Jensen D, 2015. Next-gen Transcriptomics Reveals Variable Gene Expression in Stenotrophomonas Maltophilia K279A when Grown in Co-culture with Pseudomonas Aeruginosa 2192 (Doctoral dissertation, University of Louisville).

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• Cline JM, Scott P, Kainulainen K and Weniger C, 2013. UvA-DARE (Digital Academic Repository). PHYSICAL REVIEW D Phys Rev D, 88, p.055025.

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• Peled O, Kalamaro V, Kerem E, Shoseyov D, Blau H, et al. 2014. Contamination of hypertonic saline solutions in use by cystic fibrosis patients in Israel. Journal of Cystic Fibrosis, 13(5), pp.550-556.

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• Chen T, Wang R, Lu T, Zhang Y and Wang W, 2009.Inhibitory effect of cationic polyethyleneimine polymer on penicillin antibiotics. Chinese Journal of Pharmaceutical Sciences, (9), pp. 674-678.

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• Linh NDN, Development of high-throughput sequencing analysis of fungal and respiratory microbiota in patients with cystic fibrosis.

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• Michon AL and Marchandin H, 2015. Physiopathological diversity of the respiratory microbiota. Revue Francophone des Laboratoires, 2015 (469), pp.37-49.

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• Cao W, Zhang G and Wang C, 2011. Advances in myeloid cell trigger receptor-1. Chinese Journal of Basic and Clinical Medicine, 18 (10), pp.1118-1121.

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• Elborn JS, 2011. Treating cystic fibrosis infection, inflammation and ion channels. Therapy, 8(6), pp.583-585.

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• Fasinu P, Pillay V, Ndesendo VM, du Toit LC, Choonara YE (2011) Diverse approaches for the enhancement of oral drug bioavailability. Biopharmaceutics & drug disposition 32: 185-209.

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• Stacy M (2009) Medical treatment of Parkinson disease. Neurologic clinics 27:605-631.

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• Hribar G, Žnidaršič A, Bele M, Maver U, Caserman S, et al. 2011. Zinc-phosphate nanoparticles with reversibly attached TNF-α analogs: an interesting concept for potential use in active immunotherapy. Journal of Nanoparticle Research, 13(7), pp.3019-3032.

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• Seeberger LC, Hauser RA (2007) Optimizing bioavailability in the treatment of Parkinson's disease. Neuropharmacology 53:791-800.

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• Elborn JS, 2011. Treating cystic fibrosis infection, inflammation and ion channels. Therapy, 8(6), pp.583-585.

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• Elborn JS, 2011. Treating cystic fibrosis infection, inflammation and ion channels. Therapy, 8(6), pp.583-585.

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• Chowdary KP, Shankar KR, Suchitra B (2014) Recent Research on Orodispersible Tablets-A Review. Int Res J Pharm App Sci 4: 64-73

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• Li L and Somerset S, 2014. The clinical significance of the gut microbiota in cystic fibrosis and the potential for dietary therapies. Clinical Nutrition, 33(4), pp.571-580.

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• Van Arnum P (2007) Advancing ODT technology.

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• De Boeck K, 2013. The future: from the bench to the patient. future, pp.94-103.

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• Elborn JS, 2011. Treating cystic fibrosis infection, inflammation and ion channels. Therapy, 8(6), pp.583-585.

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• Venkatesh G (2009) Granulation approaches for orally disintegrating formulations. InHandbook of Pharmaceutical Granulation Technology, Third Edition 401-434.

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• Ananthan A, Balasubramanian H, Rao S and Patole S, 2016. Probiotic supplementation in children with cystic fibrosis—a systematic review. European journal of pediatrics, 175(10), pp.1255-1266.

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• Chowdary KP, Aishwarya KV (2013) PREPARATION AND EVALUATION OF FAST DISSOLVING TABLETS OF PARACETAMOL EMPLOYING SUPERDISINTEGRANTS. Journal of global trends in Pharmaceutical Sciences 4: 1329-1334.

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• Eickmeier O, Fußbroich D, van Dullemen S, Hill C, Smaczny C, et al. 2015. Inflammation and nutrition in mucoviscidosis. The pneumologist, 12 (2), pp.148-154.

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• Chowdary KP, Aishwarya KV (2014) Preparation and evaluation of fast dissolving tablets of selected drugs employing superdisintegrants. JGTPS 5: 1392-1398.

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• McLaughlin D, Banbury S (2007) ODTs help make the medicine go down. manufacturing chemist.

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• Szakonyi G (2014) Investigation, development and evaluation of orally disintegrating tablets (Doctoral dissertation).

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• Chowdary KP, Aishwarya KV (2013) Available online at www. JGTPS. com. Journal of Global Trends in Pharmaceutical Sciences 4: 940-954.

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