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Clinical Chemistry and Laboratory Medicine|September 5, 2009
Quantitation of serum free light chains does not compensate for serum immunofixation only when screening for monoclonal gammopathiesKlas Böer, Thomas DeufelClinical Chemistry and Laboratory Medicine|April 29, 2009
Workflow restrictions on hematology analyzers XE-2100 and XS-800 when assaying pediatric samples with limited volumeKlas Böer, Thomas DeufelClinical Chemistry and Laboratory Medicine|September 11, 2010
Lactic acid is of low predictive value for the diagnosis of bacterial infection in ventricular cerebrospinal fluid samples containing residual bloodKlas Böer, Wolfgang Pfister, Michael KiehntopfExperimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|July 14, 2017
Comparison of HbA1c Measurements using 3 Methods in 75 Patients Referred to One Outpatient DepartmentJohannes Roth, Nicolle Müller, Thomas Lehmann, et al.BMC Blood Disorders|August 9, 2012
Isolated central nervous system relapse of chronic myeloid leukemia after allogeneic hematopoietic stem cell transplantationMary Fuchs, Mike Reinhöfer, Andreas Ragoschke-Schumm, et al.Mediators of Inflammation|July 18, 2015
Changes of Proteases, Antiproteases, and Pathogens in Cystic Fibrosis Patients' Upper and Lower Airways after IV-Antibiotic TherapyUlrike Müller, Julia Hentschel, Wibke K Janhsen, et al.Journal of Immunological Methods|December 28, 2013
Influences of nasal lavage collection-, processing- and storage methods on inflammatory markers--evaluation of a method for non-invasive sampling of epithelial lining fluid in cystic fibrosis and other respiratory diseasesJulia Hentschel, Ulrike Müller, Franziska Doht, et al.Rhinology|September 13, 2015
Reduced effect of intravenous antibiotic treatment on sinonasal markers in pulmonary inflammationFranziska Doht, Julia Hentschel, Nele Fischer, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|October 8, 2014
Protease-antiprotease imbalances differ between Cystic Fibrosis patients' upper and lower airway secretionsJulia Hentschel, Nele Fischer, Wibke K Janhsen, et al.Medical Microbiology and Immunology|July 6, 2016
Colonization of CF patients' upper airways with S. aureus contributes more decisively to upper airway inflammation than P. aeruginosaWibke Katharina Janhsen, Christin Arnold, Julia Hentschel, et al.Pageof 2