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Items: 1 to 50 of 82

1.

[Primary megaureter in the newborn period: making the case for a temporary splint-free cutaneous ureterostomy].

Rübben I, Vester U.

Aktuelle Urol. 2020 Apr;51(2):132-136. doi: 10.1055/a-0966-4663. Epub 2020 Jan 22. German.

PMID:
31968361
2.

HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry.

Okorn C, Goertz A, Vester U, Beck BB, Bergmann C, Habbig S, König J, Konrad M, Müller D, Oh J, Ortiz-Brüchle N, Patzer L, Schild R, Seeman T, Staude H, Thumfart J, Tönshoff B, Walden U, Weber L, Zaniew M, Zappel H, Hoyer PF, Weber S.

Pediatr Nephrol. 2019 Jun;34(6):1065-1075. doi: 10.1007/s00467-018-4188-8. Epub 2019 Jan 21.

PMID:
30666461
3.

No evidence for point mutations in the novel renal cystine transporter AGT1/SLC7A13 contributing to the etiology of cystinuria.

Olschok K, Vester U, Lahme S, Kurth I, Eggermann T.

BMC Nephrol. 2018 Oct 20;19(1):278. doi: 10.1186/s12882-018-1080-5.

4.

Author Correction: Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo.

Heinemann FM, Jindra PT, Bockmeyer CL, Zeuschner P, Wittig J, Höflich H, Eßer M, Abbas M, Dieplinger G, Stolle K, Vester U, Hoyer PF, Immenschuh S, Heinold A, Horn PA, Li W, Eisenberger U, Becker JU.

Sci Rep. 2018 Apr 12;8(1):6003. doi: 10.1038/s41598-018-23760-1.

5.

Glomerulocapillary miRNA response to HLA-class I antibody in vitro and in vivo.

Heinemann FM, Jindra PT, Bockmeyer CL, Zeuschner P, Wittig J, Höflich H, Eßer M, Abbas M, Dieplinger G, Stolle K, Vester U, Hoyer PF, Immenschuh S, Heinold A, Horn PA, Li W, Eisenberger U, Becker JU.

Sci Rep. 2017 Nov 6;7(1):14554. doi: 10.1038/s41598-017-14674-5. Erratum in: Sci Rep. 2018 Apr 12;8(1):6003.

6.

Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly.

Braun DA, Rao J, Mollet G, Schapiro D, Daugeron MC, Tan W, Gribouval O, Boyer O, Revy P, Jobst-Schwan T, Schmidt JM, Lawson JA, Schanze D, Ashraf S, Ullmann JFP, Hoogstraten CA, Boddaert N, Collinet B, Martin G, Liger D, Lovric S, Furlano M, Guerrera IC, Sanchez-Ferras O, Hu JF, Boschat AC, Sanquer S, Menten B, Vergult S, De Rocker N, Airik M, Hermle T, Shril S, Widmeier E, Gee HY, Choi WI, Sadowski CE, Pabst WL, Warejko JK, Daga A, Basta T, Matejas V, Scharmann K, Kienast SD, Behnam B, Beeson B, Begtrup A, Bruce M, Ch'ng GS, Lin SP, Chang JH, Chen CH, Cho MT, Gaffney PM, Gipson PE, Hsu CH, Kari JA, Ke YY, Kiraly-Borri C, Lai WM, Lemyre E, Littlejohn RO, Masri A, Moghtaderi M, Nakamura K, Ozaltin F, Praet M, Prasad C, Prytula A, Roeder ER, Rump P, Schnur RE, Shiihara T, Sinha MD, Soliman NA, Soulami K, Sweetser DA, Tsai WH, Tsai JD, Topaloglu R, Vester U, Viskochil DH, Vatanavicharn N, Waxler JL, Wierenga KJ, Wolf MTF, Wong SN, Leidel SA, Truglio G, Dedon PC, Poduri A, Mane S, Lifton RP, Bouchard M, Kannu P, Chitayat D, Magen D, Callewaert B, van Tilbeurgh H, Zenker M, Antignac C, Hildebrandt F.

Nat Genet. 2017 Oct;49(10):1529-1538. doi: 10.1038/ng.3933. Epub 2017 Aug 14.

7.

Mutations in DZIP1L, which encodes a ciliary-transition-zone protein, cause autosomal recessive polycystic kidney disease.

Lu H, Galeano MCR, Ott E, Kaeslin G, Kausalya PJ, Kramer C, Ortiz-Brüchle N, Hilger N, Metzis V, Hiersche M, Tay SY, Tunningley R, Vij S, Courtney AD, Whittle B, Wühl E, Vester U, Hartleben B, Neuber S, Frank V, Little MH, Epting D, Papathanasiou P, Perkins AC, Wright GD, Hunziker W, Gee HY, Otto EA, Zerres K, Hildebrandt F, Roy S, Wicking C, Bergmann C.

Nat Genet. 2017 Jul;49(7):1025-1034. doi: 10.1038/ng.3871. Epub 2017 May 22.

8.

Intermediate Follow-up of Pediatric Patients With Hemolytic Uremic Syndrome During the 2011 Outbreak Caused by E. coli O104:H4.

Loos S, Aulbert W, Hoppe B, Ahlenstiel-Grunow T, Kranz B, Wahl C, Staude H, Humberg A, Benz K, Krause M, Pohl M, Liebau MC, Schild R, Lemke J, Beringer O, Müller D, Härtel C, Wigger M, Vester U, Konrad M, Haffner D, Pape L, Oh J, Kemper MJ.

Clin Infect Dis. 2017 Jun 15;64(12):1637-1643. doi: 10.1093/cid/cix218.

PMID:
28329394
9.

Comparison of different normalization strategies for the analysis of glomerular microRNAs in IgA nephropathy.

Bockmeyer CL, Säuberlich K, Wittig J, Eßer M, Roeder SS, Vester U, Hoyer PF, Agustian PA, Zeuschner P, Amann K, Daniel C, Becker JU.

Sci Rep. 2016 Aug 24;6:31992. doi: 10.1038/srep31992.

10.

Combined liver and kidney transplantation and kidney after liver transplantation in children: Indication, postoperative outcome, and long-term results.

Büscher R, Büscher AK, Cetiner M, Treckmann JW, Paul A, Vester U, Hoyer PF.

Pediatr Transplant. 2015 Dec;19(8):858-65. doi: 10.1111/petr.12595. Epub 2015 Sep 5.

PMID:
26341656
11.

Whole-exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies.

Gee HY, Otto EA, Hurd TW, Ashraf S, Chaki M, Cluckey A, Vega-Warner V, Saisawat P, Diaz KA, Fang H, Kohl S, Allen SJ, Airik R, Zhou W, Ramaswami G, Janssen S, Fu C, Innis JL, Weber S, Vester U, Davis EE, Katsanis N, Fathy HM, Jeck N, Klaus G, Nayir A, Rahim KA, Al Attrach I, Al Hassoun I, Ozturk S, Drozdz D, Helmchen U, O'Toole JF, Attanasio M, Lewis RA, Nürnberg G, Nürnberg P, Washburn J, MacDonald J, Innis JW, Levy S, Hildebrandt F.

Kidney Int. 2014 Apr;85(4):880-7. doi: 10.1038/ki.2013.450. Epub 2013 Nov 20.

12.

Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidney-related and non-kidney-related phenotypes.

Büscher R, Büscher AK, Weber S, Mohr J, Hegen B, Vester U, Hoyer PF.

Pediatr Nephrol. 2014 Oct;29(10):1915-25. doi: 10.1007/s00467-013-2634-1. Epub 2013 Oct 10. Review.

PMID:
24114580
13.

Glomerular mRNA expression of prothrombotic and antithrombotic factors in renal transplants with thrombotic microangiopathy.

Agustian PA, Bockmeyer CL, Modde F, Wittig J, Heinemann FM, Brundiers S, Dämmrich ME, Schwarz A, Birschmann I, Suwelack B, Jindra PT, Ahlenstiel T, Wohlschläger J, Vester U, Ganzenmüller T, Zilian E, Feldkamp T, Spieker T, Immenschuh S, Kreipe HH, Bröcker V, Becker JU.

Transplantation. 2013 May 27;95(10):1242-8. doi: 10.1097/TP.0b013e318291a298.

PMID:
23635876
14.

Long-term side effects of treatment with mTOR inhibitors in children after renal transplantation.

Kranz B, Wingen AM, Vester U, König J, Hoyer PF.

Pediatr Nephrol. 2013 Aug;28(8):1293-8. doi: 10.1007/s00467-013-2459-y. Epub 2013 Apr 13.

PMID:
23584849
15.

Comprehensive analysis of glomerular mRNA expression of pro- and antithrombotic genes in atypical haemolytic-uremic syndrome (aHUS).

Modde F, Agustian PA, Wittig J, Dämmrich ME, Forstmeier V, Vester U, Ahlenstiel T, Froede K, Budde U, Wingen AM, Schwarz A, Lovric S, Kielstein JT, Bergmann C, Bachmann N, Nagel M, Kreipe HH, Bröcker V, Bockmeyer CL, Becker JU.

Virchows Arch. 2013 Apr;462(4):455-64. doi: 10.1007/s00428-013-1386-4. Epub 2013 Mar 9.

PMID:
23475501
16.

Kidney grafts from donors ≤ 5 yr of age: single kidney transplantation for pediatric recipients or en bloc transplantation for adults?

Gallinat A, Sotiropoulos GC, Witzke O, Treckmann JW, Molmenti EP, Paul A, Vester U.

Pediatr Transplant. 2013 Mar;17(2):179-84. doi: 10.1111/petr.12049.

PMID:
23442102
17.

Complement factor H-related protein 1 deficiency and factor H antibodies in pediatric patients with atypical hemolytic uremic syndrome.

Hofer J, Janecke AR, Zimmerhackl LB, Riedl M, Rosales A, Giner T, Cortina G, Haindl CJ, Petzelberger B, Pawlik M, Jeller V, Vester U, Gadner B, van Husen M, Moritz ML, Würzner R, Jungraithmayr T; German-Austrian HUS Study Group.

Clin J Am Soc Nephrol. 2013 Mar;8(3):407-15. doi: 10.2215/CJN.01260212. Epub 2012 Dec 14.

18.

An outbreak of Shiga toxin-producing Escherichia coli O104:H4 hemolytic uremic syndrome in Germany: presentation and short-term outcome in children.

Loos S, Ahlenstiel T, Kranz B, Staude H, Pape L, Härtel C, Vester U, Buchtala L, Benz K, Hoppe B, Beringer O, Krause M, Müller D, Pohl M, Lemke J, Hillebrand G, Kreuzer M, König J, Wigger M, Konrad M, Haffner D, Oh J, Kemper MJ.

Clin Infect Dis. 2012 Sep;55(6):753-9. doi: 10.1093/cid/cis531. Epub 2012 Jun 5.

PMID:
22670043
19.

Donor and recipient ACE I/D genotype are associated with loss of renal function in children following renal transplantation.

Büscher R, Nagel D, Finkelberg I, Büscher AK, Wingen AM, Kranz B, Vester U, Hoyer PF.

Pediatr Transplant. 2011 Mar;15(2):214-20. doi: 10.1111/j.1399-3046.2010.01449.x.

PMID:
21309964
20.

Early renal failure after domino liver transplantation using organs from donors with primary hyperoxaluria type 1.

Saner FH, Treckmann J, Pratschke J, Arbogast H, Rahmel A, Vester U, Paul A.

Transplantation. 2010 Oct 15;90(7):782-5. doi: 10.1097/TP.0b013e3181eefe1f.

PMID:
20671595
21.

Complement inhibitor eculizumab in atypical hemolytic uremic syndrome.

Mache CJ, Acham-Roschitz B, Frémeaux-Bacchi V, Kirschfink M, Zipfel PF, Roedl S, Vester U, Ring E.

Clin J Am Soc Nephrol. 2009 Aug;4(8):1312-6. doi: 10.2215/CJN.01090209. Epub 2009 Jun 25.

22.

Young man with kidney failure and hemorrhagic interstitial nephritis.

Lordemann AG, Hjelle B, Theegarten D, Grabellus F, Schmid KW, Hoyer PF, Vester U, Becker JU.

Am J Kidney Dis. 2009 Dec;54(6):1162-6. doi: 10.1053/j.ajkd.2009.04.025. Epub 2009 Jun 25. No abstract available.

PMID:
19556044
23.

Eculizumab for atypical hemolytic-uremic syndrome.

Nürnberger J, Philipp T, Witzke O, Opazo Saez A, Vester U, Baba HA, Kribben A, Zimmerhackl LB, Janecke AR, Nagel M, Kirschfink M.

N Engl J Med. 2009 Jan 29;360(5):542-4. doi: 10.1056/NEJMc0808527. No abstract available. Erratum in: N Engl J Med. 2009 Jun 4;360(23):2487. Philipp, Thomas [added].

PMID:
19179328
24.

Identification of novel cystinuria mutations in pediatric patients.

Brauers E, Hozyasz K, Golabek B, Slowik M, Schmidt C, Vester U, Zerres K, Eggermann T.

J Pediatr Urol. 2006 Dec;2(6):575-8. doi: 10.1016/j.jpurol.2005.11.011. Epub 2006 Jan 19.

PMID:
18947684
25.

The diagnostic value of ultrasound in cystic kidney diseases.

Vester U, Kranz B, Hoyer PF.

Pediatr Nephrol. 2010 Feb;25(2):231-40. doi: 10.1007/s00467-008-0981-0. Epub 2008 Sep 23. Review.

26.

Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.

Dietrich A, Matejas V, Bitzan M, Hashmi S, Kiraly-Borri C, Lin SP, Mildenberger E, Hoppe B, Palm L, Shiihara T, Steiss JO, Tsai JD, Vester U, Weber S, Wühl E, Zepf K, Zenker M.

Pediatr Nephrol. 2008 Oct;23(10):1779-86. doi: 10.1007/s00467-008-0880-4. Epub 2008 Jul 2.

PMID:
18594871
27.

Nephrectomy in an autosomal recessive polycystic kidney disease (ARPKD) patient with rapid kidney enlargement and increased expression of EGFR.

Arbeiter A, Büscher R, Bonzel KE, Wingen AM, Vester U, Wohlschläger J, Zerres K, Nürnberger J, Bergmann C, Hoyer PF.

Nephrol Dial Transplant. 2008 Sep;23(9):3026-9. doi: 10.1093/ndt/gfn288. Epub 2008 May 23. No abstract available.

PMID:
18503009
28.

Acute rejection episodes in pediatric renal transplant recipients with cytomegalovirus infection.

Kranz B, Vester U, Wingen AM, Nadalin S, Paul A, Broelsch CE, Hoyer PF.

Pediatr Transplant. 2008 Jun;12(4):474-8. doi: 10.1111/j.1399-3046.2007.00781.x.

PMID:
18466436
29.

Cyclosporine-A-induced nephrotoxicity in children with minimal-change nephrotic syndrome: long-term treatment up to 10 years.

Kranz B, Vester U, Büscher R, Wingen AM, Hoyer PF.

Pediatr Nephrol. 2008 Apr;23(4):581-6. doi: 10.1007/s00467-007-0709-6. Epub 2008 Jan 16.

30.

Effect of growth hormone therapy on nitric oxide formation in cystic fibrosis patients.

Grasemann C, Ratjen F, Schnabel D, Reutershahn E, Vester U, Grasemann H.

Eur Respir J. 2008 Apr;31(4):815-21. Epub 2007 Dec 19.

31.

Current concepts in transplant surgery: laparoscopic living donor of the kidney.

Paul A, Treckmann J, Gallinat A, Witzke O, Vester U, Broelsch CE.

Langenbecks Arch Surg. 2007 Sep;392(5):501-9. Epub 2007 May 26.

PMID:
17530281
32.

The symptomatic pelvic kidney: a new source of organs for living donor kidney transplantation?

Li J, Nadalin S, Paul A, Sotiropoulos GC, Broelsch CE, Kranz B, Vester U, Schaffer R, Philipp T, Otto T.

Transplantation. 2006 Nov 15;82(9):1241-2. No abstract available.

PMID:
17102780
33.

Acute scrotum in a neonate.

Vester U, Bender HU, Sperling H, Hoyer P.

Ultraschall Med. 2006 Oct;27(5):410-1. English, German. No abstract available. Erratum in: Ultraschall Med. 2006 Dec;27(6):511. Vester, U [added]; Bender, H U [added]; Sperling, H [added]; Hoyer, P [added].

PMID:
17033942
34.

Outcome after kidney transplantation in children with thrombotic risk factors.

Kranz B, Vester U, Nadalin S, Paul A, Broelsch CE, Hoyer PF.

Pediatr Transplant. 2006 Nov;10(7):788-93.

PMID:
17032424
35.

Decreased systemic bioavailability of L-arginine in patients with cystic fibrosis.

Grasemann H, Schwiertz R, Grasemann C, Vester U, Racké K, Ratjen F.

Respir Res. 2006 Jun 9;7:87.

36.

Antiviral treatment of chronic hepatitis B with lamivudine in pediatric renal transplantation.

Kranz B, Vester U, Bonzel KE, Paul A, Gerken G, Hoyer PF.

Pediatr Transplant. 2006 May;10(3):384-9.

PMID:
16677367
37.

Unusual manifestation of posttransplant lymphoproliferative disorder in the esophagus.

Kranz B, Vester U, Becker J, Woltering T, Wingen AM, Paul A, Hoyer PF.

Transplant Proc. 2006 Apr;38(3):693-6.

PMID:
16647447
38.

Search for mutations in SLC1A5 (19q13) in cystinuria patients.

Brauers E, Vester U, Zerres K, Eggermann T.

J Inherit Metab Dis. 2005;28(6):1169-71.

PMID:
16435221
39.

Oedema with proteinuria in Gambian children--a descriptive study.

Archer HA, van der Sande M, Hoyer P, Goetghebuer T, McAdam KP, Vester U, Newport MJ.

Pediatr Nephrol. 2006 Mar;21(3):339-43. Epub 2006 Jan 11.

PMID:
16404628
40.

Multi-exon deletions of the PKHD1 gene cause autosomal recessive polycystic kidney disease (ARPKD).

Bergmann C, Küpper F, Schmitt CP, Vester U, Neuhaus TJ, Senderek J, Zerres K.

J Med Genet. 2005 Oct;42(10):e63.

41.

Development of growth and body mass index after pediatric renal transplantation.

Vester U, Schaefer A, Kranz B, Wingen AM, Nadalin S, Paul A, Malagò M, Broelsch CE, Hoyer PF.

Pediatr Transplant. 2005 Aug;9(4):445-9.

PMID:
16048595
42.

Sirolimus rescue of renal failure in children after combined liver-kidney transplantation.

Vester U, Kranz B, Nadalin S, Paul A, Becker J, Hoyer PF.

Pediatr Nephrol. 2005 May;20(5):686-9. Epub 2005 Feb 19.

PMID:
15723197
43.

The response to cyclophosphamide in steroid-sensitive nephrotic syndrome is influenced by polymorphic expression of glutathion-S-transferases-M1 and -P1.

Vester U, Kranz B, Zimmermann S, Büscher R, Hoyer PF.

Pediatr Nephrol. 2005 Apr;20(4):478-81. Epub 2005 Feb 17.

PMID:
15717164
44.

Clinical consequences of PKHD1 mutations in 164 patients with autosomal-recessive polycystic kidney disease (ARPKD).

Bergmann C, Senderek J, Windelen E, Küpper F, Middeldorf I, Schneider F, Dornia C, Rudnik-Schöneborn S, Konrad M, Schmitt CP, Seeman T, Neuhaus TJ, Vester U, Kirfel J, Büttner R, Zerres K; APN (Arbeitsgemeinschaft für Pädiatrische Nephrologie).

Kidney Int. 2005 Mar;67(3):829-48.

45.

Oral L-arginine supplementation in cystic fibrosis patients: a placebo-controlled study.

Grasemann H, Grasemann C, Kurtz F, Tietze-Schillings G, Vester U, Ratjen F.

Eur Respir J. 2005 Jan;25(1):62-8.

46.

Removal of metabolites, cytokines and hepatic growth factors by extracorporeal liver support in children.

Auth MK, Kim HS, Beste M, Bonzel KE, Baumann U, Ballauff A, Wallot M, Borchers T, Vester U, Grasemann C, Hauffa B, Hoyer PF, Gerken G, Voit T.

J Pediatr Gastroenterol Nutr. 2005 Jan;40(1):54-9.

PMID:
15625427
47.

Absorption phase cyclosporine (C(2h)) monitoring in the first weeks after pediatric renal transplantation.

Vester U, Kranz B, Offner G, Nadalin S, Paul A, Broelsch CE, Hoyer PE.

Pediatr Nephrol. 2004 Nov;19(11):1273-7.

PMID:
15365805
48.

Pathomechanisms and the diagnosis of arterial hypertension in pediatric renal allograft recipients.

Büscher R, Vester U, Wingen AM, Hoyer PF.

Pediatr Nephrol. 2004 Nov;19(11):1202-11. Review.

PMID:
15365804
49.

No evidence for a role of SLC7A10 in 19q13 in the etiology of cystinuria.

Schmidt C, Vester U, Zerres K, Eggermann T.

Clin Nephrol. 2004 Jul;62(1):71-3. No abstract available.

PMID:
15267019
50.

Medical and surgical aspects of pediatric renal transplantation using living donors.

Vester U, Kranz B, Testa G, Paul A, Broelsch CE, Hoyer PF.

Transplant Proc. 2004 Jun;36(5):1308-10.

PMID:
15251319

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