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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.
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