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404 results
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Atypical distal renal tubular acidosis confirmed by mutation analysis.
Weber S, Soergel M, Jeck N, Konrad M. Weber S, et al. Among authors: konrad m. Pediatr Nephrol. 2000 Dec;15(3-4):201-4. doi: 10.1007/s004670000454. Pediatr Nephrol. 2000. PMID: 11149111
Treatment and long-term outcome in primary distal renal tubular acidosis.
Lopez-Garcia SC, Emma F, Walsh SB, Fila M, Hooman N, Zaniew M, Bertholet-Thomas A, Colussi G, Burgmaier K, Levtchenko E, Sharma J, Singhal J, Soliman NA, Ariceta G, Basu B, Murer L, Tasic V, Tsygin A, Decramer S, Gil-Peña H, Koster-Kamphuis L, La Scola C, Gellermann J, Konrad M, Lilien M, Francisco T, Tramma D, Trnka P, Yüksel S, Caruso MR, Chromek M, Ekinci Z, Gambaro G, Kari JA, König J, Taroni F, Thumfart J, Trepiccione F, Winding L, Wühl E, Ağbaş A, Belkevich A, Vargas-Poussou R, Blanchard A, Conti G, Boyer O, Dursun I, Pınarbaşı AS, Melek E, Miglinas M, Novo R, Mallett A, Milosevic D, Szczepanska M, Wente S, Cheong HI, Sinha R, Gucev Z, Dufek S, Iancu D; European dRTA Consortium, Kleta R, Schaefer F, Bockenhauer D. Lopez-Garcia SC, et al. Among authors: konrad m. Nephrol Dial Transplant. 2019 Jun 1;34(6):981-991. doi: 10.1093/ndt/gfy409. Nephrol Dial Transplant. 2019. PMID: 30773598
Gene locus ambiguity in posterior urethral valves/prune-belly syndrome.
Weber S, Mir S, Schlingmann KP, Nürnberg G, Becker C, Kara PE, Ozkayin N, Konrad M, Nürnberg P, Schaefer F. Weber S, et al. Among authors: konrad m. Pediatr Nephrol. 2005 Aug;20(8):1036-42. doi: 10.1007/s00467-005-1977-7. Epub 2005 May 24. Pediatr Nephrol. 2005. PMID: 15912376
Hypomagnesemia with hypercalciuria and nephrocalcinosis: case report and a family study.
Tasic V, Dervisov D, Koceva S, Weber S, Konrad M. Tasic V, et al. Among authors: konrad m. Pediatr Nephrol. 2005 Jul;20(7):1003-6. doi: 10.1007/s00467-005-1853-5. Epub 2005 Apr 26. Pediatr Nephrol. 2005. PMID: 15856319
Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.
Wolf MT, Dötsch J, Konrad M, Böswald M, Rascher W. Wolf MT, et al. Among authors: konrad m. Pediatr Nephrol. 2002 Aug;17(8):602-8. doi: 10.1007/s00467-002-0884-4. Epub 2002 Jun 11. Pediatr Nephrol. 2002. PMID: 12185465
Recent advances in molecular genetics of hereditary magnesium-losing disorders.
Konrad M, Weber S. Konrad M, et al. J Am Soc Nephrol. 2003 Jan;14(1):249-60. doi: 10.1097/01.asn.0000049161.60740.ce. J Am Soc Nephrol. 2003. PMID: 12506158 Review.
Dealing with the incidental finding of secondary variants by the example of SRNS patients undergoing targeted next-generation sequencing.
Weber S, Büscher AK, Hagmann H, Liebau MC, Heberle C, Ludwig M, Rath S, Alberer M, Beissert A, Zenker M, Hoyer PF, Konrad M, Klein HG, Hoefele J. Weber S, et al. Among authors: konrad m. Pediatr Nephrol. 2016 Jan;31(1):73-81. doi: 10.1007/s00467-015-3167-6. Epub 2015 Aug 7. Pediatr Nephrol. 2016. PMID: 26248470
Medullary nephrocalcinosis in a pediatric patient.
Altugan FS, Ozçakar ZB, Fitöz S, Ensari A, Ekim M, Konrad M, Yalçinkaya F. Altugan FS, et al. Among authors: konrad m. Pediatr Nephrol. 2010 Aug;25(8):1429-30, 1431-3. doi: 10.1007/s00467-009-1374-8. Epub 2009 Dec 9. Pediatr Nephrol. 2010. PMID: 19997941 No abstract available.
Clinical course and NPHS2 analysis in patients with late steroid-resistant nephrotic syndrome.
Schwaderer P, Knüppel T, Konrad M, Mehls O, Schärer K, Schaefer F, Weber S. Schwaderer P, et al. Among authors: konrad m. Pediatr Nephrol. 2008 Feb;23(2):251-6. doi: 10.1007/s00467-007-0653-5. Epub 2007 Nov 14. Pediatr Nephrol. 2008. PMID: 18000687
Candesartan cilexetil in children with hypertension or proteinuria: preliminary data.
Simonetti GD, von Vigier RO, Konrad M, Rizzi M, Fossali E, Bianchetti MG. Simonetti GD, et al. Among authors: konrad m. Pediatr Nephrol. 2006 Oct;21(10):1480-2. doi: 10.1007/s00467-006-0144-0. Epub 2006 Jun 27. Pediatr Nephrol. 2006. PMID: 16802178 Clinical Trial.
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