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Presentation of pediatric Henoch-Schönlein purpura nephritis changes with age and renal histology depends on biopsy timing.
Hennies I, Gimpel C, Gellermann J, Möller K, Mayer B, Dittrich K, Büscher AK, Hansen M, Aulbert W, Wühl E, Nissel R, Schalk G, Weber LT, Pohl M, Wygoda S, Beetz R, Klaus G, Fehrenbach H, König S, Staude H, Beringer O, Bald M, Walden U, von Schnakenburg C, Bertram G, Wallot M, Häffner K, Wiech T, Hoyer PF, Pohl M; German Society of Pediatric Nephrology. Hennies I, et al. Among authors: von schnakenburg c. Pediatr Nephrol. 2018 Feb;33(2):277-286. doi: 10.1007/s00467-017-3794-1. Epub 2017 Oct 5. Pediatr Nephrol. 2018. PMID: 28983704
Primary hyperoxaluria--the German experience.
Hoppe B, Latta K, von Schnakenburg C, Kemper MJ. Hoppe B, et al. Am J Nephrol. 2005 May-Jun;25(3):276-81. doi: 10.1159/000086358. Epub 2005 Jun 15. Am J Nephrol. 2005. PMID: 15961947
Note of caution for the use of sodium nitroprusside in neonatal hypertension.
von Schnakenburg C, Krüger M. von Schnakenburg C, et al. Pediatr Nephrol. 2004 Nov;19(11):1307; author reply 1308-9. doi: 10.1007/s00467-004-1557-2. Epub 2004 Aug 25. Pediatr Nephrol. 2004. PMID: 15338387 No abstract available.
Complete remission of post-transplant FSGS recurrence by long-term plasmapheresis.
Häffner K, Zimmerhackl LB, von Schnakenburg C, Brandis M, Pohl M. Häffner K, et al. Pediatr Nephrol. 2005 Jul;20(7):994-7. doi: 10.1007/s00467-005-1858-0. Epub 2005 May 12. Pediatr Nephrol. 2005. PMID: 15889282
[Pseudo-Acanthosis nigricans in a 12 year old boy after kidney transplantation].
von Schnakenburg C, Enke B, Jürgens K, Offner G. von Schnakenburg C, et al. Klin Padiatr. 2001 Sep-Oct;213(5):288-9. doi: 10.1055/s-2001-17221. Klin Padiatr. 2001. PMID: 11582528 German.
Post-transplant epididymitis and orchitis following Listeria monocytogenes septicaemia.
von Schnakenburg C, Hinrichs B, Fuchs J, Kardorff R. von Schnakenburg C, et al. Pediatr Transplant. 2000 May;4(2):156-8. doi: 10.1034/j.1399-3046.2000.00113.x. Pediatr Transplant. 2000. PMID: 11272610
Genetic analysis: a diagnostic tool for primary hyperoxaluria type 1.
von Schnakenburg C, Rumsby G, Hoppe B, Latta K, Kemper M. von Schnakenburg C, et al. Pediatr Nephrol. 2003 May;18(5):482-3; author reply 484. doi: 10.1007/s00467-003-1107-3. Epub 2003 Apr 5. Pediatr Nephrol. 2003. PMID: 12687460 No abstract available.
Identification of new mutations in primary hyperoxaluria type 1 (PH1).
von Schnakenburg C, Rumsby G. von Schnakenburg C, et al. J Nephrol. 1998 Mar-Apr;11 Suppl 1:15-7. J Nephrol. 1998. PMID: 9604803
Variable presentation of primary hyperoxaluria type 1 in 2 patients homozygous for a novel combined deletion and insertion mutation in exon 8 of the AGXT gene.
von Schnakenburg C, Hulton SA, Milford DV, Roper HP, Rumsby G. von Schnakenburg C, et al. Nephron. 1998;78(4):485-8. doi: 10.1159/000044979. Nephron. 1998. PMID: 9578076
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