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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|February 19, 2026
The kidney in genetic metabolic disordersUlla T Schultheiss, Anke Schumann
JIMD Reports|November 7, 2022
Severe loss of appetite and refusal to eat as severe side effect of glycerol phenylbutyrateSarah Catharina Grünert, Anke Schumann, Ute Spiekerkoetter
Molecular Genetics and Metabolism|August 19, 2023
Clinical and biochemical footprints of inherited metabolic diseases. XIV. Metabolic kidney diseasesAnke Schumann, Ulla T Schultheiss, Carlos R Ferreira, et al.
Clinical Biochemistry|December 14, 2023
A systematic review of metabolomic findings in adult and pediatric renal diseaseLennart Moritz, Anke Schumann, Martin Pohl, et al.
Molecular Genetics and Metabolism Reports|May 24, 2021
Successful pregnancy in a woman with glycogen storage disease type 6Sarah Catharina Grünert, Stefanie Rosenbaum-Fabian, Luciana Hannibal, et al.
Plos One|October 10, 2022
I'm fine with collecting data: Engagement profiles differ depending on scientific activities in an online community of a citizen science projectTill Bruckermann, Hannah Greving, Milena Stillfried, et al.
JIMD Reports|January 21, 2021
Three successful pregnancies in a patient with glycogen storage disease type 0Sarah C Grünert, Stefanie Rosenbaum-Fabian, Luciana Hannibal, et al.
Genes|July 29, 2023
Riboflavin 1 Transporter Deficiency: Novel SLC52A1 Variants and Expansion of the Phenotypic SpectrumSarah C Grünert, Athanasia Ziagaki, André Heinen, et al.
Genes|November 27, 2021
Evidence for a Genotype-Phenotype Correlation in Patients with Pathogenic GLUT2 (SLC2A2) VariantsSarah C Grünert, Anke Schumann, Federico Baronio, et al.
Nutrition Journal|May 14, 2018
Successful pregnancy in maple syrup urine disease: a case report and review of the literatureSarah Catharina Grünert, Stefanie Rosenbaum-Fabian, Anke Schumann, et al.
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