Anibh M. Das

Medizinische Hochschule Hannover — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

44h-index6.7kcitations243works2.12yr avg
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Research Topics

Metabolism and Genetic Disorders(104), Mitochondrial Function and Pathology(53), Lysosomal Storage Disorders Research(41), Neonatal Health and Biochemistry(31), Amino Acid Enzymes and Metabolism(28)

Publications243 total

Lipid-dependent uptake of pegunigalsidase alfa across cell types: Implications for multiorgan treatment
Molecular Genetics and Metabolism·2026Open Access
Kidney Injury Urine Biomarker Normal Ranges in Children
Kidney International Reports·2026Open Access
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 Vitro
Nutrients·2026Open Access
Overview of European practices for management of tyrosinemia type 1
DiRROS repository (University of Maribor)·2025
Successful methionine treatment for diffuse lung disease in a child with pathogenic MARS-1 gene variants
Klinische Pädiatrie·2025
REBALANCING REPRODUCTION: AN AYURVEDIC CASE STUDY IN PCOS AND UTERINE FIBROID MANAGEMENT
International Journal of Advanced Research·2025Open Access
Ascorbate mitigates oxidative stress and hemin cytotoxicity in heme oxygenase-1 deficiency
Journal of Biological Chemistry·2025Open Access
Ascorbate mitigates oxidative stress and hemin cytotoxicity in heme oxygenase-1 deficiency
FreiDok plus (Universitätsbibliothek Freiburg)·2025Open Access
Overview of European Practices for Management of Tyrosinemia Type 1: Towards European Guidelines
Journal of Inherited Metabolic Disease·2025· 2 citedOpen Access
Medical Expert Knowledge Meets AI to Enhance Symptom Checker Performance for Rare Disease Identification in Fabry Disease: Mixed Methods Study
JMIR AI·2025· 2 citedOpen Access
Clinicopathological Dimensions of Renal Amyloidosis: A Comprehensive Study from a Tertiary Care Center
The Journal of Medical Sciences·2025Open Access
Urea cycle defects in adulthood: clinical presentation, diagnosis and treatment in genetically encoded hepatic metabolic disorders with a potential for encephalopathy
Metabolic Brain Disease·2025· 1 citedOpen Access
Success of methionine supplementation for treatment of alveolar proteinosis with confirmed MARS-1 mutation: a case report
Klinische Pädiatrie·2025
Cellular uptake and function of recombinant pegunigalsidase alfa in fibroblasts from Fabry patients
Molecular Genetics and Metabolism·2025
Diagnosis, treatment, management and monitoring of patients with tyrosinaemia type 1: Consensus group recommendations from the German‐speaking countries
Journal of Inherited Metabolic Disease·2024· 5 citedOpen Access
The European reference network for metabolic diseases (MetabERN) clinical pathway recommendations for Pompe disease (acid maltase deficiency, glycogen storage disease type II)
Orphanet Journal of Rare Diseases·2024· 17 citedOpen Access
Rosa canina L. Methanol Extract and Its Component Rutin Reduce Cholesterol More Efficiently than Miglustat in Niemann–Pick C Fibroblasts
International Journal of Molecular Sciences·2024Open Access
Treatment with 2-phospho-L-ascorbic acid mitigates biochemical phenotypes of heme oxygenase 1 deficiency
2024Open Access
Simplification of Dietary Treatment in Pharmacoresistant Epilepsy: Impact of C8 and C10 Fatty Acids on Sirtuins of Neuronal Cells In Vitro
Nutrients·2024· 3 citedOpen Access
Brain function in classic galactosemia, a galactosemia network (GalNet) members review
Frontiers in Genetics·2024· 12 citedOpen Access
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Frequent Co-authors

Thomas Lücke(10), Hans Hartmann(8), Frits A. Wijburg(7), Martin Lindner(7), René Santer(7), Matthias R. Baumgartner(7), Sabine Illsinger(7), Julia B. Hennermann(6), Barbara Plecko(6), Ulrike Steuerwald(6), Stefanie Sander(6), Georg F. Hoffmann(5), Uta Meyer(5), Johannes Sander(5), Stefan Kölker(5), Nils Janzen(5), Ute Spiekerkoetter(4), Daniela Karall(4), Hans-Georg Koch(4), Karl Otfried Schwab(4)