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The Application of Clinical Genetics|August 4, 2017
Clinical utility of nitisinone for the treatment of hereditary tyrosinemia type-1 (HT-1)Anibh Martin Das
Metabolic Brain Disease|April 26, 2025
Urea cycle defects in adulthood: clinical presentation, diagnosis and treatment in genetically encoded hepatic metabolic disorders with a potential for encephalopathyAnibh Martin Das
Nutrients|January 28, 2026
Towards Simplification of Ketogenic Diet in Epilepsy: Effect of Caprylic (C8) and Capric (C10) Acid on the Mitochondrial Respiratory Chain in Murine Hippocampal Neurons In VitroMiriam Rebekka Rühling, Hans Hartmann, Anibh Martin Das
Nutrients|June 19, 2024
Simplification of Dietary Treatment in Pharmacoresistant Epilepsy: Impact of C8 and C10 Fatty Acids on Sirtuins of Neuronal Cells In VitroMiriam Rebekka Rühling, Hans Hartmann, Anibh Martin Das
Orphanet Journal of Rare Diseases|November 29, 2014
Glycogen storage disease type III: modified Atkins diet improves myopathySebene Mayorandan, Uta Meyer, Hans Hartmann, et al.
Pharmaceutical Medicine|June 4, 2026
Optimising Formulations for Paediatric Patients with Inherited Metabolic Disorders: The Case Study of LevocarnitineStephen Tomlin, Chris Mühlhausen, Andriy Krendyukov, et al.
Plos One|October 24, 2017
Alterations of sirtuins in mitochondrial cytochrome c-oxidase deficiencyArne Björn Potthast, Theresa Heuer, Simone Johanna Warneke, et al.
Metabolism: Clinical and Experimental|December 5, 2006
Elevated plasma concentrations of the endogenous nitric oxide synthase inhibitor asymmetric dimethylarginine in citrullinemiaThomas Lücke, Dimitrios Tsikas, Nele Kanzelmeyer, et al.
European Journal of Pediatrics|July 22, 2006
Pitfalls in paediatric gait disturbances: painless bone diseasesThomas Lücke, Sabine Illsinger, Anibh Martin Das, et al.
Klinische Padiatrie|May 3, 2017
[Lysosomal Storage Diseases: Challenges in Multiprofessional Patient Care with Enzyme Replacement Therapy]Anibh Martin Das, Florian Lagler, Michael Beck, et al.
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