Showing results (181-190 of 189) with videos related to
Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 189 results.
Journal of the American Society of Nephrology : JASN|May 23, 2003
A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2Rainer G Ruf, Matthias T F Wolf, Hans C Hennies, et al.Biochimica Et Biophysica Acta|October 30, 2004
Identification and characterisation of a novel KCNQ1 mutation in a family with Romano-Ward syndromeJ Zehelein, D Thomas, M Khalil, et al.Journal of the American Society of Nephrology : JASN|February 24, 2004
Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndromeRainer G Ruf, Anne Lichtenberger, Stephanie M Karle, et al.Kidney International|July 16, 2004
Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndromeRainer G Ruf, Michael Schultheiss, Anne Lichtenberger, et al.Atherosclerosis|March 21, 2006
Unmet needs in the diagnosis and treatment of dyslipidemia in the primary care setting in GermanyS Böhler, H Scharnagl, F Freisinger, et al.Zentralblatt Fur Chirurgie|May 23, 2007
[Report on the workshop "workflow rectal cancer II" in Burghausen]R Bittner, J Burghardt, E Gross, et al.Zentralblatt Fur Chirurgie|May 23, 2007
[Quality indicators for diagnostic and therapy of rectal carcinoma]R Bittner, J Burghardt, E Gross, et al.Nature Genetics|July 23, 2003
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determinationEdgar A Otto, Bernhard Schermer, Tomoko Obara, et al.Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.Pageof 19