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The Laryngoscope|December 14, 2021
Hearing Loss and Its Burden of Disease in a Large German Cohort-Hearing Loss in GermanyBerit Hackenberg, Julia Döge, Karl J Lackner, et al.Transplant International : Official Journal of the European Society for Organ Transplantation|December 5, 2003
Recurrence of Budd-Chiari syndrome after liver transplantation in paroxysmal nocturnal hemoglobinuriaMatthias J Bahr, Jörg Schubert, Jörg S Bleck, et al.Nucleic Acids Research|January 6, 2010
The ribosome assembly factor Nep1 responsible for Bowen-Conradi syndrome is a pseudouridine-N1-specific methyltransferaseJan Philip Wurm, Britta Meyer, Ute Bahr, et al.Gastroenterology Research and Practice|November 19, 2009
Clinical relevance of transjugular liver biopsy in comparison with percutaneous and laparoscopic liver biopsyMax G Beckmann, Matthias J Bahr, Johannes Hadem, et al.European Heart Journal|November 26, 2008
Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseasesNathalie Gaborit, Thomas Wichter, Andras Varro, et al.Vaccine|December 1, 1990
Mycobacterium vaccae in immunoprophylaxis and immunotherapy of leprosy and tuberculosisJ L Stanford, G A Rook, G M Bahr, et al.Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|December 5, 2012
Reconstitution of interleukin-17-producing T helper cells after allogeneic hematopoietic cell transplantationFelix Bahr, Rebekka Wehner, Uwe Platzbecker, et al.Plos One|July 11, 2013
A heterozygous deletion mutation in the cardiac sodium channel gene SCN5A with loss- and gain-of-function characteristics manifests as isolated conduction disease, without signs of Brugada or long QT syndromeSven Zumhagen, Marieke W Veldkamp, Birgit Stallmeyer, et al.Journal of Synchrotron Radiation|August 18, 2012
The new ambient-pressure X-ray photoelectron spectroscopy instrument at MAX-labJoachim Schnadt, Jan Knudsen, Jesper N Andersen, et al.Lancet (London, England)|October 31, 2001
Molecular diagnosis in a child with sudden infant death syndromeP J Schwartz, S G Priori, R Bloise, et al.Pageof 281