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Anibh M Das

Showing results (11-20 of 91) with videos related to

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Metabolic Brain Disease|September 17, 2005
Mitochondrial function in schimke-immunoosseous dysplasiaThomas Lücke, Jochen H H Ehrich, Anibh M Das
BMC Gastroenterology|September 1, 2012
Macro-AST: misleading finding in an adolescent with MCAD-deficiencyAnibh M Das, Sabine Drache, Nils Janzen, et al.
Nutrients|December 23, 2020
Ketogenic Diet: Impact on Cellular Lipids in Hippocampal Murine NeuronsPartha Dabke, Graham Brogden, Hassan Y Naim, et al.
Annals of Nutrition & Metabolism|April 2, 2010
Glycogen storage disease type 1: impact of medium-chain triglycerides on metabolic control and growthAnibh M Das, Thomas Lücke, Uta Meyer, et al.
Molecular Genetics and Metabolism|April 28, 2004
Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblastsThomas Lücke, Wiebke Höppner, Esther Schmidt, et al.
Pediatric Neurology|May 29, 2003
BH4-sensitive hyperphenylalaninemia: new case and review of literatureThomas Lücke, Sabine Illsinger, Christa Aulehla-Scholz, et al.
Pediatric Neurology|March 23, 2004
3-methylglutaconic aciduria type I in a boy with fever-associated seizuresSabine Illsinger, Thomas Lücke, Johannes Zschocke, et al.
Clinical Chemistry and Laboratory Medicine|September 26, 2007
Developmental changes in the L-arginine/nitric oxide pathway from infancy to adulthood: plasma asymmetric dimethylarginine levels decrease with ageThomas Lücke, Nele Kanzelmeyer, Markus J Kemper, et al.
Orphanet Journal of Rare Diseases|December 23, 2017
Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosisNils Janzen, Alejandro D Hofmann, Gunnar Schmidt, et al.
Advances in Experimental Medicine and Biology|July 30, 2017
Dietary Considerations in Tyrosinemia Type IFrancjan J van Spronsen, Margreet van Rijn, Uta Meyer, et al.
Pageof 10

Showing results (11-20 of 91) with videos related to

Sort By:
Pageof 10
Metabolic Brain Disease|September 17, 2005
Mitochondrial function in schimke-immunoosseous dysplasiaThomas Lücke, Jochen H H Ehrich, Anibh M Das
BMC Gastroenterology|September 1, 2012
Macro-AST: misleading finding in an adolescent with MCAD-deficiencyAnibh M Das, Sabine Drache, Nils Janzen, et al.
Nutrients|December 23, 2020
Ketogenic Diet: Impact on Cellular Lipids in Hippocampal Murine NeuronsPartha Dabke, Graham Brogden, Hassan Y Naim, et al.
Annals of Nutrition & Metabolism|April 2, 2010
Glycogen storage disease type 1: impact of medium-chain triglycerides on metabolic control and growthAnibh M Das, Thomas Lücke, Uta Meyer, et al.
Molecular Genetics and Metabolism|April 28, 2004
Fabry disease: reduced activities of respiratory chain enzymes with decreased levels of energy-rich phosphates in fibroblastsThomas Lücke, Wiebke Höppner, Esther Schmidt, et al.
Pediatric Neurology|May 29, 2003
BH4-sensitive hyperphenylalaninemia: new case and review of literatureThomas Lücke, Sabine Illsinger, Christa Aulehla-Scholz, et al.
Pediatric Neurology|March 23, 2004
3-methylglutaconic aciduria type I in a boy with fever-associated seizuresSabine Illsinger, Thomas Lücke, Johannes Zschocke, et al.
Clinical Chemistry and Laboratory Medicine|September 26, 2007
Developmental changes in the L-arginine/nitric oxide pathway from infancy to adulthood: plasma asymmetric dimethylarginine levels decrease with ageThomas Lücke, Nele Kanzelmeyer, Markus J Kemper, et al.
Orphanet Journal of Rare Diseases|December 23, 2017
Non-invasive test using palmitate in patients with suspected fatty acid oxidation defects: disease-specific acylcarnitine patterns can help to establish the diagnosisNils Janzen, Alejandro D Hofmann, Gunnar Schmidt, et al.
Advances in Experimental Medicine and Biology|July 30, 2017
Dietary Considerations in Tyrosinemia Type IFrancjan J van Spronsen, Margreet van Rijn, Uta Meyer, et al.
Pageof 10