Publications by authors named "Ludwig Patzer"

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Growth dynamics of transversal body dimensions and proportions, with related clinical determinants in children with X-linked hypophosphatemia treated with phosphate supplements and active vitamin D.
Laura Celine Brieger, Stephan Przygodda, Alina Verena Bohlen, Mirko Rehberg, Martin Konrad, Ludwig Patzer

Pediatr Nephrol· October 2025

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Office Blood Pressure and Obesity in Children with X-Linked Hypophosphatemia.
Ineke Böckmann, Maren Leifheit-Nestler, Mirko Rehberg, Giuseppina Spartà, Katrina Evers, Ludwig Patzer

Calcif Tissue Int· March 2025

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Health-related quality of life of children with X-linked hypophosphatemia in Germany.
Martin Klein, Michael Obermaier, Helena Mutze, Sophia Maria Wilden, Mirko Rehberg, Ludwig Patzer

Pediatr Nephrol· November 2024

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Renal and Extrarenal Phenotypes in Patients With Variants and Chromosome 17q12 Microdeletions.
Bénédicte Buffin-Meyer, Juliette Richard, Vincent Guigonis, Stefanie Weber, Jens König, Ludwig Patzer

Kidney Int Rep· August 2024

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Is there a dominant-negative effect in individuals with heterozygous disease-causing variants in COL4A3/COL4A4?
Korbinian M Riedhammer, Hannes Simmendinger, Velibor Tasic, Jovana Putnik, Nora Abazi-Emini, Ludwig Patzer

Clin Genet· April 2024

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Effects of Burosumab Treatment on Mineral Metabolism in Children and Adolescents With X-linked Hypophosphatemia.
Annika Ewert, Mirko Rehberg, Karl Peter Schlingmann, Olaf Hiort, Ulrike John-Kroegel, Ludwig Patzer

J Clin Endocrinol Metab· September 2023

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Potential Benefit of Probiotic E. Coli Nissle in Term Neonates.
Dirk Olbertz, Hans Proquitté, Ludwig Patzer, Thomas Erler, Alexsandra Mikolajczak

Klin Padiatr· July 2023

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Correction: Potential Benefit of Probiotic E. Coli Nissle in Term Neonates.
Dirk Olbertz, Hans Proquitté, Ludwig Patzer, Thomas Erler, Alexsandra Mikolajczak

Klin Padiatr· July 2023

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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, Ludwig Patzer

Front Med (Lausanne)· October 2022

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Relationship between age at initiation of cysteamine treatment, adherence with therapy, and glomerular kidney function in infantile nephropathic cystinosis.
Christina Nießl, Anne-Laure Boulesteix, Jun Oh, Katja Palm, Peter Schlingmann, Ludwig Patzer

Mol Genet Metab· August 2022

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Patients With Infantile Nephropathic Cystinosis in Germany and Austria: A Retrospective Cohort Study.
Nina O'Connell, Jun Oh, Klaus Arbeiter, Anja Büscher, Dieter Haffner, Ludwig Patzer

Front Med (Lausanne)· April 2022

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Systematic evaluation of olfaction in patients with hereditary cystic kidney diseases/renal ciliopathies.
Mareike Dahmer-Heath, Valentin Schriever, Sabine Kollmann, Carolin Schleithoff, Andrea Titieni, Ludwig Patzer

J Med Genet· September 2021

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Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants.
Kathrin Burgmaier, Leonie Brinker, Florian Erger, Bodo B Beck, Marcus R Benz, Ludwig Patzer

Kidney Int· September 2021

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Severe neurological outcomes after very early bilateral nephrectomies in patients with autosomal recessive polycystic kidney disease (ARPKD).
Kathrin Burgmaier, Gema Ariceta, Martin Bald, Anja Katrin Buescher, Mathias Burgmaier, Ludwig Patzer

Sci Rep· September 2020

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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.
Christine Okorn, Anne Goertz, Udo Vester, Bodo B Beck, Carsten Bergmann, Ludwig Patzer

Pediatr Nephrol· June 2019

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Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.
Karl P Schlingmann, Justyna Ruminska, Martin Kaufmann, Ismail Dursun, Monica Patti, Ludwig Patzer

J Am Soc Nephrol· February 2016

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Diagnosis of Alport syndrome--search for proteomic biomarkers in body fluids.
Michael Pohl, Karin Danz, Oliver Gross, Ulrike John, Johannes Urban, Ludwig Patzer

Pediatr Nephrol· November 2013

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Long-term follow-up after rituximab for steroid-dependent idiopathic nephrotic syndrome.
Markus J Kemper, Jutta Gellermann, Sandra Habbig, Rafael T Krmar, Katalin Dittrich, Ludwig Patzer

Nephrol Dial Transplant· May 2012

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Oligohydramnios associated with sonographically normal kidneys.
Ulrike John, Kerstin Benz, Axel Hübler, Ludwig Patzer, Martin Zenker

Urology· May 2012

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Age-related penetrance of hereditary atypical hemolytic uremic syndrome.
Maren Sullivan, Lisa A Rybicki, Aurelia Winter, Michael M Hoffmann, Stefanie Reiermann, Ludwig Patzer

Ann Hum Genet· November 2011

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Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndrome.
Maren Sullivan, Zoran Erlic, Michael M Hoffmann, Klaus Arbeiter, Ludwig Patzer

Ann Hum Genet· January 2010

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Nephrotoxicity as a cause of acute kidney injury in children.
Ludwig Patzer

Pediatr Nephrol· December 2008

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Growth impairment after ifosfamide-induced nephrotoxicity in children.
Wolfgang Stöhr, Ludwig Patzer, Marios Paulides, Anja Kremers, Jörn-Dirk Beck

Pediatr Blood Cancer· May 2007

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Blood pressure, renal function, and proteinuria in children with unilateral renal agenesis.
Tomás Seeman, Ludwig Patzer, Ulrike John, Jirí Dusek, Karel Vondrák

Kidney Blood Press Res· January 2007

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Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.
Rainer G Ruf, Michael Schultheiss, Anne Lichtenberger, Stephanie M Karle, Isabella Zalewski, Ludwig Patzer

Kidney Int· August 2004

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