Year |
Citation |
Score |
2019 |
Szczesniak RD, Brokamp C, Su W, Mcphail GL, Pestian J, Clancy JP. Improving Detection of Rapid Cystic Fibrosis Disease Progression-Early Translation of a Predictive Algorithm Into a Point-of-Care Tool. Ieee Journal of Translational Engineering in Health and Medicine. 7: 2800108. PMID 30800534 DOI: 10.1109/Jtehm.2018.2878534 |
0.379 |
|
2018 |
McCrory BE, Harper HN, McPhail GL. Use and Incidence of Adverse Effects of Proton Pump Inhibitors in Patients with Cystic Fibrosis. Pharmacotherapy. PMID 29800488 DOI: 10.1002/Phar.2125 |
0.302 |
|
2016 |
Harris WT, Boyd JT, McPhail GL, Brody AS, Szczesniak RD, Korbee LL, Baker ML, Clancy JP. Constrictive Bronchiolitis in Adolescents with Cystic Fibrosis with Refractory Pulmonary Decline. Annals of the American Thoracic Society. PMID 27684511 DOI: 10.1513/Annalsats.201412-594Oc |
0.417 |
|
2015 |
Szczesniak RD, McPhail GL, Li D, Amin RS, Clancy JP. Predicting future lung function decline in cystic fibrosis patients: Statistical methods and clinical connections. Pediatric Pulmonology. PMID 26677806 DOI: 10.1002/Ppul.23357 |
0.395 |
|
2015 |
Brewington JJ, McPhail GL, Clancy JP. Lumacaftor alone and combined with ivacaftor: preclinical and clinical trial experience of F508del CFTR correction. Expert Review of Respiratory Medicine. 1-13. PMID 26581802 DOI: 10.1586/17476348.2016.1122527 |
0.32 |
|
2015 |
Kotha K, Szczesniak RD, Naren AP, Fenchel MC, Duan LL, McPhail GL, Clancy JP. Concentration of fractional excretion of nitric oxide (FENO): A potential airway biomarker of restored CFTR function. Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society. PMID 26210165 DOI: 10.1016/J.Jcf.2015.07.002 |
0.349 |
|
2015 |
McPhail GL, Ehsan Z, Howells SA, Boesch RP, Fenchel MC, Szczesniak R, Jain V, Agabegi S, Sturm P, Wall E, Redding GJ. Obstructive lung disease in children with idiopathic scoliosis. The Journal of Pediatrics. 166: 1018-21. PMID 25684085 DOI: 10.1016/J.Jpeds.2014.12.070 |
0.417 |
|
2015 |
McPhail G, Chini B, Siracusa C, Fenchel M, Szczesniak R, Clancy J. 211 Vitamin D insufficiency is associated with pulmonary exacerbations in children with cystic fibrosis Journal of Cystic Fibrosis. 14: S112. DOI: 10.1016/S1569-1993(15)30387-8 |
0.318 |
|
2014 |
Siracusa CM, Weiland JL, Acton JD, Chima AK, Chini BA, Hoberman AJ, Wetzel JD, Amin RS, McPhail GL. The impact of transforming healthcare delivery on cystic fibrosis outcomes: a decade of quality improvement at Cincinnati Children's Hospital. Bmj Quality & Safety. 23: i56-i63. PMID 24608552 DOI: 10.1136/Bmjqs-2013-002361 |
0.375 |
|
2014 |
Clancy J, Amin R, Szczesniak R, Mcphail G, Fleck R. WS3.3 MRI-based pulmonary blood flow and lung function in CF patients – flow changes with pulmonary decline Journal of Cystic Fibrosis. 13: S6. DOI: 10.1016/S1569-1993(14)60021-7 |
0.388 |
|
2013 |
McPhail GL, Howells SA, Boesch RP, Wood RE, Ednick M, Chini BA, Jain V, Agabegi S, Sturm P, Wall E, Crawford A, Redding G. Obstructive lung disease is common in children with syndromic and congenital scoliosis: a preliminary study. Journal of Pediatric Orthopedics. 33: 781-5. PMID 24172682 DOI: 10.1097/Bpo.0000000000000078 |
0.383 |
|
2013 |
Szczesniak RD, McPhail GL, Duan LL, Macaluso M, Amin RS, Clancy JP. A semiparametric approach to estimate rapid lung function decline in cystic fibrosis. Annals of Epidemiology. 23: 771-7. PMID 24103586 DOI: 10.1016/J.Annepidem.2013.08.009 |
0.403 |
|
2013 |
VanDyke RD, McPhail GL, Huang B, Fenchel MC, Amin RS, Carle AC, Chini BA, Seid M. Inhaled tobramycin effectively reduces FEV1 decline in cystic fibrosis. An instrumental variables analysis. Annals of the American Thoracic Society. 10: 205-12. PMID 23802816 DOI: 10.1513/Annalsats.201209-082Oc |
0.411 |
|
2013 |
Fleck R, McPhail G, Szczesniak R, Knowlton J, Radhakrishnan R, Clancy J, Amin R. Aortopulmonary collateral flow in cystic fibrosis assessed with phase-contrast MRI. Pediatric Radiology. 43: 1279-86. PMID 23677424 DOI: 10.1007/S00247-013-2708-Z |
0.397 |
|
2013 |
Grossoehme DH, Szczesniak R, McPhail GL, Seid M. Is adolescents' religious coping with cystic fibrosis associated with the rate of decline in pulmonary function?-A preliminary study. Journal of Health Care Chaplaincy. 19: 33-42. PMID 23551049 DOI: 10.1080/08854726.2013.767083 |
0.402 |
|
2013 |
Grossoehme DH, Cotton S, McPhail G. Use and sanctification of complementary and alternative medicine by parents of children with cystic fibrosis. Journal of Health Care Chaplaincy. 19: 22-32. PMID 23551048 DOI: 10.1080/08854726.2013.761007 |
0.339 |
|
2012 |
Piccione JC, McPhail GL, Fenchel MC, Brody AS, Boesch RP. Bronchiectasis in chronic pulmonary aspiration: risk factors and clinical implications. Pediatric Pulmonology. 47: 447-52. PMID 22028069 DOI: 10.1002/Ppul.21587 |
0.361 |
|
2010 |
McPhail GL, Weiland J, Acton JD, Ednick M, Chima A, VanDyke R, Fenchel MC, Amin RS, Seid M. Improving evidence-based care in cystic fibrosis through quality improvement. Archives of Pediatrics & Adolescent Medicine. 164: 957-60. PMID 20921354 DOI: 10.1001/Archpediatrics.2010.178 |
0.39 |
|
2010 |
McPhail GL, Ednick MD, Fenchel MC, VanDyke R, Chima A, Amin RS, Seid M. Improving follow-up in hospitalised children. Quality & Safety in Health Care. 19: e35. PMID 20511243 DOI: 10.1136/Qshc.2009.034538 |
0.324 |
|
2010 |
McPhail GL. Coagulation disorder as a presentation of cystic fibrosis. The Journal of Emergency Medicine. 38: 320-2. PMID 18385006 DOI: 10.1016/J.Jemermed.2007.10.038 |
0.335 |
|
2008 |
McPhail GL, Acton JD, Fenchel MC, Amin RS, Seid M. Improvements in lung function outcomes in children with cystic fibrosis are associated with better nutrition, fewer chronic pseudomonas aeruginosa infections, and dornase alfa use. The Journal of Pediatrics. 153: 752-7. PMID 18760423 DOI: 10.1016/J.Jpeds.2008.07.011 |
0.43 |
|
2008 |
McPhail GL, Hardie WD. Cavitary lung lesions in a 2-year-old child. Respiration; International Review of Thoracic Diseases. 76: 117-8. PMID 17975297 DOI: 10.1159/000110743 |
0.305 |
|
2006 |
McPhail GL, Hardie WD. POSTTRAUMATIC PULMONARY PSEUDOCYST IN A 2-YEAR-OLD CHILD Chest. 130: 319S. DOI: 10.1378/Chest.130.4_Meetingabstracts.319S-B |
0.343 |
|
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