Publications by authors named "Martin Kirschstein"

Claim this Profile
D
Diagnostic Yield and Benefits of Whole Exome Sequencing in CAKUT Patients Diagnosed in the First Thousand Days of Life.
Lina Werfel, Helge Martens, Imke Hennies, Ann Christin Gjerstad, Kerstin Fröde, Martin Kirschstein

Kidney Int Rep· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age.
Roman Günthner, Lea Knipping, Stefanie Jeruschke, Robin Satanoskij, Bettina Lorenz-Depiereux, Martin Kirschstein

Front Med (Lausanne)· October 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Correction to: Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Verena Klämbt, Charlotte Gimpel, Martin Bald, Christopher Gerken, Heiko Billing, Martin Kirschstein

Pediatr Nephrol· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[What is confirmed in the treatment of autoinflammatory fever diseases?].
Anne Pankow, Eugen Feist, Ulrich Baumann, Martin Kirschstein, Gerd-Rüdiger Burmester

Internist (Berl)· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Different approaches to long-term treatment of aHUS due to MCP mutations: a multicenter analysis.
Verena Klämbt, Charlotte Gimpel, Martin Bald, Christopher Gerken, Heiko Billing, Martin Kirschstein

Pediatr Nephrol· February 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rare co-occurrence of osteogenesis imperfecta type I and autosomal dominant polycystic kidney disease.
Julia Hoefele, Karin Mayer, Christoph Marschall, Martin Alberer, Hanns-Georg Klein, Martin Kirschstein

World J Pediatr· November 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel mutation within the lactase gene (LCT): the first report of congenital lactase deficiency diagnosed in Central Europe.
Walid Fazeli, Sigrid Kaczmarek, Martin Kirschstein, René Santer

BMC Gastroenterol· July 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Urinary proteome analysis to exclude severe vesicoureteral reflux.
Jens Drube, Eric Schiffer, Esther Lau, Claus Petersen, Martin Kirschstein

Pediatrics· February 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Urinary proteome analysis identifies infants but not older children requiring pyeloplasty.
Jens Drube, Petra Zürbig, Eric Schiffer, Esther Lau, Benno Ure, Martin Kirschstein

Pediatr Nephrol· September 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Acute focal bacterial nephritis in 25 children.
Tanja Seidel, Eberhard Kuwertz-Bröking, Sigrid Kaczmarek, Martin Kirschstein, Michael Frosch

Pediatr Nephrol· November 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
IgACE: a placebo-controlled, randomized trial of angiotensin-converting enzyme inhibitors in children and young people with IgA nephropathy and moderate proteinuria.
Rosanna Coppo, Licia Peruzzi, Alessandro Amore, Antonio Piccoli, Pierre Cochat, Martin Kirschstein

J Am Soc Nephrol· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Prenatal diagnosis of parenchymal kidney diseases].
Martin Kirschstein, Reinhard Jensen, Ulrich Gembruch, Christof Sohn

Z Geburtshilfe Neonatol· March 2003

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis