Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

41 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.
Sadowski CE, Lovric S, Ashraf S, Pabst WL, Gee HY, Kohl S, Engelmann S, Vega-Warner V, Fang H, Halbritter J, Somers MJ, Tan W, Shril S, Fessi I, Lifton RP, Bockenhauer D, El-Desoky S, Kari JA, Zenker M, Kemper MJ, Mueller D, Fathy HM, Soliman NA; SRNS Study Group; Hildebrandt F. Sadowski CE, et al. J Am Soc Nephrol. 2015 Jun;26(6):1279-89. doi: 10.1681/ASN.2014050489. Epub 2014 Oct 27. J Am Soc Nephrol. 2015. PMID: 25349199 Free PMC article.
[Diagnosis of congenital dilatation of the urinary tract. Consensus Group of the Pediatric Nephrology Working Society in cooperation with the Pediatric Urology Working Group of the German Society of Urology and with the Pediatric Urology Working Society in the Germany Society of Pediatric Surgery].
Beetz R, Bökenkamp A, Brandis M, Hoyer P, John U, Kemper MJ, Kirschstein M, Kuwertz-Bröking E, Misselwitz J, Müller-Wiefel DE, Rascher W. Beetz R, et al. Among authors: kirschstein m. Urologe A. 2001 Nov;40(6):495-507; quiz 508-9. doi: 10.1007/s001200170015. Urologe A. 2001. PMID: 11760359 Review. German. No abstract available.
Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Klämbt V, Gimpel C, Bald M, Gerken C, Billing H, Loos S, Hansen M, König J, Vinke T, Montoya C, Lange-Sperandio B, Kirschstein M, Hennies I, Pohl M, Häffner K. Klämbt V, et al. Among authors: kirschstein m. Pediatr Nephrol. 2021 Feb;36(2):463-471. doi: 10.1007/s00467-020-04714-0. Epub 2020 Jul 26. Pediatr Nephrol. 2021. PMID: 32715379 Free PMC article.
Urinary proteome analysis to exclude severe vesicoureteral reflux.
Drube J, Schiffer E, Lau E, Petersen C, Kirschstein M, Kemper MJ, Lichtinghagen R, Ure B, Mischak H, Pape L, Ehrich JH. Drube J, et al. Among authors: kirschstein m. Pediatrics. 2012 Feb;129(2):e356-63. doi: 10.1542/peds.2010-3467. Epub 2012 Jan 23. Pediatrics. 2012. PMID: 22271698
Correction to: Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Klämbt V, Gimpel C, Bald M, Gerken C, Billing H, Loos S, Hansen M, König J, Vinke T, Montoya C, Lange-Sperandio B, Kirschstein M, Hennies I, Pohl M, Häffner K. Klämbt V, et al. Among authors: kirschstein m. Pediatr Nephrol. 2021 Dec;36(12):4015. doi: 10.1007/s00467-021-05292-5. Pediatr Nephrol. 2021. PMID: 34553238 Free PMC article. No abstract available.
[Prenatal diagnosis of parenchymal kidney diseases].
Kirschstein M, Jensen R, Gembruch U, Sohn C. Kirschstein M, et al. Z Geburtshilfe Neonatol. 2002 Sep-Oct;206(5):203. doi: 10.1055/s-2002-34960. Z Geburtshilfe Neonatol. 2002. PMID: 12395295 German. No abstract available.
41 results