Anibh M. Das
Department of Paediatrics
Hannover Medical School
Carl-Neuberg Str
1, D-30625
Germany
Name/email consistency: high
- Macro-AST: misleading finding in an adolescent with MCAD-deficiency. Das, A.M., Drache, S., Janzen, N., Franke, A. BMC. Gastroenterol (2012)
- Inborn errors of energy metabolism associated with myopathies. Das, A.M., Steuerwald, U., Illsinger, S. J. Biomed. Biotechnol. (2010)
- Prenatal benzoate treatment in urea cycle defects. Das, A.M., Illsinger, S., Hartmann, H., Oehler, K., Bohnhorst, B., Kühn-Velten, W.N., Lücke, T. Arch. Dis. Child. Fetal Neonatal Ed. (2009)
- Biochemical basis of Fabry disease with emphasis on mitochondrial function and protein trafficking. Das, A.M., Naim, H.Y. Adv. Clin. Chem (2009)
- Isolated mitochondrial long-chain ketoacyl-CoA thiolase deficiency resulting from mutations in the HADHB gene. Das, A.M., Illsinger, S., Lücke, T., Hartmann, H., Ruiter, J.P., Steuerwald, U., Waterham, H.R., Duran, M., Wanders, R.J. Clin. Chem. (2006)
- Glutaric aciduria I: creatine supplementation restores creatinephosphate levels in mixed cortex cells from rat incubated with 3-hydroxyglutarate. Das, A.M., Lücke, T., Ullrich, K. Mol. Genet. Metab. (2003)
- Regulation of the mitochondrial ATP-synthase in health and disease. Das, A.M. Mol. Genet. Metab. (2003)
- Altered levels of high-energy phosphate compounds in fibroblasts from different forms of neuronal ceroid lipofuscinoses: further evidence for mitochondrial involvement. Das, A.M., von Harlem, R., Feist, M., Lücke, T., Kohlschütter, A. Eur. J. Paediatr. Neurol. (2001)
