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JIMD Reports|July 13, 2022
Two successful pregnancies and first use of empagliflozin during pregnancy in glycogen storage disease type IbSarah Catharina Grünert, Stefanie Rosenbaum-Fabian, Anke Schumann, et al.
Journal of Inherited Metabolic Disease|May 16, 2020
Organic acidurias: Major gaps, new challenges, and a yet unfulfilled promiseBianca Dimitrov, Femke Molema, Monique Williams, et al.
Scientific Reports|May 11, 2023
The impact of metabolic stressors on mitochondrial homeostasis in a renal epithelial cell model of methylmalonic aciduriaAnke Schumann, Marion Brutsche, Monique Havermans, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|September 29, 2025
Pitfalls in the diagnosis of carnitine palmitoyltransferase 1 deficiencySarah C Grünert, Urs Berger, Friederike Hörster, et al.
Orphanet Journal of Rare Diseases|October 24, 2019
Unsuccessful intravenous D-mannose treatment in PMM2-CDGSarah C Grünert, Thorsten Marquardt, Ekkehart Lausch, et al.
Plos One|April 8, 2026
The influence of psychological ownership on pride in a Citizen Science project on wildlife ecologyHannah Greving, Till Bruckermann, Anke Schumann, et al.
Environmental Pollution (Barking, Essex : 1987)|January 3, 2022
Evaluating the potential of urban areas for bat conservation with citizen science dataDaniel Lewanzik, Tanja M Straka, Julia Lorenz, et al.
Orphanet Journal of Rare Diseases|April 12, 2020
Primary carnitine deficiency - diagnosis after heart transplantation: better late than never!Sarah C Grünert, Sara Tucci, Anke Schumann, et al.
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