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Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|April 30, 2003
Allografting after nonmyeloablative conditioning as a treatment after a failed conventional hematopoietic cell transplantLyle C Feinstein, Brenda M Sandmaier, David G Maloney, et al.Urology Practice|August 28, 2024
Practice Readiness? Trends in Chief Resident Case Logs vs Subsequent Case Log Data in Clinical PracticeZachary Corey, Erik Lehman, Gary E Lemack, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|December 29, 2023
Longitudinal changes in the cystic fibrosis airway microbiota with time and treatmentGisli G Einarsson, Laura J Sherrard, Joseph E Hatch, et al.Journal of Endourology|February 12, 2026
Residual Stone Volume Predicts Health Care Consumption and Stone Events: Analysis of Two-Year Results of the ASPIRE StudyBrian R Matlaga, Thomas J Mueller, Brett Johnson, et al.The European Respiratory Journal|June 28, 2018
Anaerobic bacteria cultured from cystic fibrosis airways correlate to milder disease: a multisite studyMarianne S Muhlebach, Joseph E Hatch, Gisli G Einarsson, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 5, 2013
BIIL 284 reduces neutrophil numbers but increases P. aeruginosa bacteremia and inflammation in mouse lungsGerd Döring, Alessandra Bragonzi, Moira Paroni, et al.Biology of Reproduction|October 14, 2024
Functional characterization of human recessive DIS3 variants in premature ovarian insufficiency†Brianna L Kline, Nicole A Siddall, Fernando Wijaya, et al.Physiological Genomics|December 24, 2009
EDNRA variants associate with smooth muscle mRNA levels, cell proliferation rates, and cystic fibrosis pulmonary disease severityRebecca Darrah, Edward McKone, Clare O'Connor, et al.The European Respiratory Journal|July 15, 2017
Characterisation of eppin function: expression and activity in the lungAaron Scott, Arlene Glasgow, Donna Small, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 7, 2019
CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trialsScott C Bell, Peter J Barry, Kris De Boeck, et al.Pageof 172