Research ExplorerPublications[Obstructive nephropathy]

[Obstructive nephropathy]

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[Obstructive nephropathy]. / Ringert, R-H; Riedmiller, H; Rübben, H; Rose, A; Hoyer, P F; Conrad, S; Hoang-Böhm, J; Müller-Wiefel, Dirk E.

In: UROLOGE, Vol. 45, No. 4, 4, 2006, p. 225-228.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Ringert, R-H, Riedmiller, H, Rübben, H, Rose, A, Hoyer, PF, Conrad, S, Hoang-Böhm, J & Müller-Wiefel, DE 2006, '[Obstructive nephropathy]', UROLOGE, vol. 45, no. 4, 4, pp. 225-228. <http://www.ncbi.nlm.nih.gov/pubmed/16937123?dopt=Citation>

APA

Ringert, R-H., Riedmiller, H., Rübben, H., Rose, A., Hoyer, P. F., Conrad, S., Hoang-Böhm, J., & Müller-Wiefel, D. E. (2006). [Obstructive nephropathy]. UROLOGE, 45(4), 225-228. [4]. http://www.ncbi.nlm.nih.gov/pubmed/16937123?dopt=Citation

Vancouver

Ringert R-H, Riedmiller H, Rübben H, Rose A, Hoyer PF, Conrad S et al. [Obstructive nephropathy]. UROLOGE. 2006;45(4):225-228. 4.

Bibtex

@article{3e09503cda4845c296b7af1a643d3cb8,
title = "[Obstructive nephropathy]",
abstract = "Congenital anomalies of the kidney and urinary tract (CAKUT) are regarded as a single entity. The degree of obstruction may have an additional influence on the parenchymal malfunction. Congenital dilatation of the upper urinary tract associated with symptomatic urinary tract infection must be treated early with intensive antibiotic therapy. In some cases temporary urinary diversion is also required. Further diagnostic procedures are then postponed in such cases. In all other cases of dilatation of the upper urinary tract diagnosed prenatally or early in the postnatal period, diuresis renography is still the cornerstone of diagnosis, even though it has definite limitations in young infants and in babies with poor kidney function. Functional gadolinum MR-urography will become the method of choice in the near future, since it combines good functional and excellent morphological presentation. When an obstruction hampering function is definitely present surgical correction is indicated: open and endoscopic surgery yield similarly good results. Molecular markers in CAKUT may soon be used as prognostic indicators. Examination of the molecular alterations that occur in renal and urinary tract anomalies may also lead to medicamentous protection of renal function.",
author = "R-H Ringert and H Riedmiller and H R{\"u}bben and A Rose and Hoyer, {P F} and S Conrad and J Hoang-B{\"o}hm and M{\"u}ller-Wiefel, {Dirk E.}",
year = "2006",
language = "Deutsch",
volume = "45",
pages = "225--228",
journal = "UROLOGE",
issn = "0340-2592",
publisher = "Springer",
number = "4",

}

RIS

TY - JOUR

T1 - [Obstructive nephropathy]

AU - Ringert, R-H

AU - Riedmiller, H

AU - Rübben, H

AU - Rose, A

AU - Hoyer, P F

AU - Conrad, S

AU - Hoang-Böhm, J

AU - Müller-Wiefel, Dirk E.

PY - 2006

Y1 - 2006

N2 - Congenital anomalies of the kidney and urinary tract (CAKUT) are regarded as a single entity. The degree of obstruction may have an additional influence on the parenchymal malfunction. Congenital dilatation of the upper urinary tract associated with symptomatic urinary tract infection must be treated early with intensive antibiotic therapy. In some cases temporary urinary diversion is also required. Further diagnostic procedures are then postponed in such cases. In all other cases of dilatation of the upper urinary tract diagnosed prenatally or early in the postnatal period, diuresis renography is still the cornerstone of diagnosis, even though it has definite limitations in young infants and in babies with poor kidney function. Functional gadolinum MR-urography will become the method of choice in the near future, since it combines good functional and excellent morphological presentation. When an obstruction hampering function is definitely present surgical correction is indicated: open and endoscopic surgery yield similarly good results. Molecular markers in CAKUT may soon be used as prognostic indicators. Examination of the molecular alterations that occur in renal and urinary tract anomalies may also lead to medicamentous protection of renal function.

AB - Congenital anomalies of the kidney and urinary tract (CAKUT) are regarded as a single entity. The degree of obstruction may have an additional influence on the parenchymal malfunction. Congenital dilatation of the upper urinary tract associated with symptomatic urinary tract infection must be treated early with intensive antibiotic therapy. In some cases temporary urinary diversion is also required. Further diagnostic procedures are then postponed in such cases. In all other cases of dilatation of the upper urinary tract diagnosed prenatally or early in the postnatal period, diuresis renography is still the cornerstone of diagnosis, even though it has definite limitations in young infants and in babies with poor kidney function. Functional gadolinum MR-urography will become the method of choice in the near future, since it combines good functional and excellent morphological presentation. When an obstruction hampering function is definitely present surgical correction is indicated: open and endoscopic surgery yield similarly good results. Molecular markers in CAKUT may soon be used as prognostic indicators. Examination of the molecular alterations that occur in renal and urinary tract anomalies may also lead to medicamentous protection of renal function.

M3 - SCORING: Zeitschriftenaufsatz

VL - 45

SP - 225

EP - 228

JO - UROLOGE

JF - UROLOGE

SN - 0340-2592

IS - 4

M1 - 4

ER -