Utsch B - Search Results

Year	Number of Results
1998	1
1999	1
2001	2
2002	3
2003	2
2004	3
2005	7
2006	6
2007	5
2008	2
2009	2
2010	1
2011	2
2014	3
2015	1
2019	2
2020	2
2021	4
2022	1
2024	0

1

Utsch B, Klaus G. Utsch B, et al. Dtsch Arztebl Int. 2014 Sep 12;111(37):617-25; quiz 626. doi: 10.3238/arztebl.2014.0617. Dtsch Arztebl Int. 2014. PMID: 25283761 Free PMC article. Review.

2

Genetic and molecular aspects of hypospadias.

Utsch B, Albers N, Ludwig M. Utsch B, et al. Eur J Pediatr Surg. 2004 Oct;14(5):297-302. doi: 10.1055/s-2004-821275. Eur J Pediatr Surg. 2004. PMID: 15543478 Review.

3

[Lower urinary tract obstruction (LUTO)--clinical picture, prenatal diagnostics and therapeutic options].

Bildau J, Enzensberger C, Degenhardt J, Kawecki A, Tenzer A, Kohl T, Stressig R, Ritgen J, Utsch B, Axt-Fliedner R. Bildau J, et al. Among authors: utsch b. Z Geburtshilfe Neonatol. 2014 Feb;218(1):18-26. doi: 10.1055/s-0034-1367042. Epub 2014 Mar 4. Z Geburtshilfe Neonatol. 2014. PMID: 24595911 Review. German.

4

A novel stable polyalanine [poly(A)] expansion in the HOXA13 gene associated with hand-foot-genital syndrome: proper function of poly(A)-harbouring transcription factors depends on a critical repeat length?

Utsch B, Becker K, Brock D, Lentze MJ, Bidlingmaier F, Ludwig M. Utsch B, et al. Hum Genet. 2002 May;110(5):488-94. doi: 10.1007/s00439-002-0712-8. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073020 Review.

5

Transvascular kidney biopsy in adolescent patients-safe alternative to open procedures.

Utsch B, Hoppe H, Dittrich K, Amann K, Gugger M, Tschumi S, Galiano M, Plank C, Rascher W, Schmid A, Uder M, Dötsch J. Utsch B, et al. Clin Kidney J. 2020 Jun 18;14(1):451-453. doi: 10.1093/ckj/sfaa092. eCollection 2021 Jan. Clin Kidney J. 2020. PMID: 33564456 Free PMC article. No abstract available.

6

Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease.

Ludwig M, Utsch B, Monnens LA. Ludwig M, et al. Among authors: utsch b. Nephrol Dial Transplant. 2006 Oct;21(10):2708-17. doi: 10.1093/ndt/gfl346. Epub 2006 Jul 20. Nephrol Dial Transplant. 2006. PMID: 16861240 Review. No abstract available.

7

Evidence of oligogenic inheritance in nephronophthisis.

Hoefele J, Wolf MT, O'Toole JF, Otto EA, Schultheiss U, Dêschenes G, Attanasio M, Utsch B, Antignac C, Hildebrandt F. Hoefele J, et al. Among authors: utsch b. J Am Soc Nephrol. 2007 Oct;18(10):2789-95. doi: 10.1681/ASN.2007020243. Epub 2007 Sep 12. J Am Soc Nephrol. 2007. PMID: 17855640

8

Novel NCCT gene mutations as a cause of Gitelman's syndrome and a systematic review of mutant and polymorphic NCCT alleles.

Reissinger A, Ludwig M, Utsch B, Prömse A, Baulmann J, Weisser B, Vetter H, Kramer HJ, Bokemeyer D. Reissinger A, et al. Among authors: utsch b. Kidney Blood Press Res. 2002;25(6):354-62. doi: 10.1159/000068695. Kidney Blood Press Res. 2002. PMID: 12590198 Review.

9

Hypercalciuria in patients with CLCN5 mutations.

Ludwig M, Utsch B, Balluch B, Fründ S, Kuwertz-Bröking E, Bökenkamp A. Ludwig M, et al. Among authors: utsch b. Pediatr Nephrol. 2006 Sep;21(9):1241-50. doi: 10.1007/s00467-006-0172-9. Epub 2006 Jun 29. Pediatr Nephrol. 2006. PMID: 16807762

10

[Genetic and molecular biological aspects of the bladder exstrophy-epispadias complex (BEEC)].

Ludwig M, Utsch B, Reutter H. Ludwig M, et al. Among authors: utsch b. Urologe A. 2005 Sep;44(9):1037-8, 1040-4. doi: 10.1007/s00120-005-0863-z. Urologe A. 2005. PMID: 15973548 Review. German.

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