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The Journal of Biological Chemistry|September 13, 2000
Low chloride stimulation of prostaglandin E2 release and cyclooxygenase-2 expression in a mouse macula densa cell lineT Yang, J M Park, L Arend, et al.
Transplantation Proceedings|February 12, 2008
Renal transplantation in children with lower urinary tract dysfunction of different origin: a single-center experienceY Bilginer, F T Aki, R Topaloglu, et al.
Kidney International|August 1, 1996
Molecular basis of hereditary C1q deficiency associated with SLE and IgA nephropathy in a Turkish familyR Topaloglu, A Bakkaloglu, J H Slingsby, et al.
Journal of Medical Genetics|February 5, 2003
A phenocopy of CAII deficiency: a novel genetic explanation for inherited infantile osteopetrosis with distal renal tubular acidosisK J Borthwick, N Kandemir, R Topaloglu, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|October 26, 2007
Interferon-gamma assays for the diagnosis of tuberculosis infection before using tumour necrosis factor-alpha blockersN Cobanoglu, U Ozcelik, U Kalyoncu, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|May 31, 2013
Disparities in policies, practices and rates of pediatric kidney transplantation in EuropeJ Harambat, K J van Stralen, F Schaefer, et al.
Transplantation Proceedings|June 4, 2013
The CERTAIN Registry: a novel, web-based registry and research platform for pediatric renal transplantation in EuropeL Plotnicki, C D Kohl, B Höcker, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|November 29, 2015
Impact of Everolimus and Low-Dose Cyclosporin on Cytomegalovirus Replication and Disease in Pediatric Renal TransplantationB Höcker, S Zencke, L Pape, et al.
Journal of Medical Genetics|November 5, 2002
Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing lossE H Stover, K J Borthwick, C Bavalia, et al.
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