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Thorsten Marquardt

Showing results (1-10 of 142) with videos related to

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Nature Medicine|May 4, 2004
A COG in the sugar machineThorsten Marquardt
Biochimica Et Biophysica Acta|January 20, 2009
Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now?Jonas Denecke, Thorsten Marquardt
Frontiers in Genetics|September 27, 2021
Treatment Options in Congenital Disorders of GlycosylationJulien H Park, Thorsten Marquardt
Pharmaceuticals (Basel, Switzerland)|September 28, 2023
Improved Enzyme Replacement Therapy with Cipaglucosidase Alfa/Miglustat in Infantile Pompe DiseaseLina Fiege, Ibrahim Duran, Thorsten Marquardt
The New England Journal of Medicine|May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyThorsten Marquardt, Eva Morava, Stephan Rust
Nutrition (Burbank, Los Angeles County, Calif.)|December 18, 2018
Long-term ketone body therapy of severe multiple acyl-CoA dehydrogenase deficiency: A case reportTobias Fischer, Ulrike Och, Thorsten Marquardt
Endocrinology, Diabetes & Metabolism Case Reports|August 16, 2023
Managing type 1 diabetes mellitus with a ketogenic dietClemens Gardemann, Sonja Knowles, Thorsten Marquardt
Brain : a Journal of Neurology|January 22, 2020
Reply: Not every excessive startle is hyperekplexia, the curious case of SOD1Julien H Park, Christiane Elpers, Thorsten Marquardt
Bioorganic & Medicinal Chemistry|November 5, 2002
Membrane-permeant derivatives of mannose-1-phosphateSynke Rutschow, Joachim Thiem, Christian Kranz, et al.
Nutrients|August 10, 2024
Influence of Carbohydrate Intake on Caprylic Acid (C8:0)-Induced Ketogenesis-A Systematic Review and Meta-AnalysisMarius Frenser, Tobias Fischer, Isabel Albrecht, et al.
Pageof 15

Showing results (1-10 of 142) with videos related to

Sort By:
Pageof 15
Nature Medicine|May 4, 2004
A COG in the sugar machineThorsten Marquardt
Biochimica Et Biophysica Acta|January 20, 2009
Congenital dyserythropoietic anemia type II (CDAII/HEMPAS): where are we now?Jonas Denecke, Thorsten Marquardt
Frontiers in Genetics|September 27, 2021
Treatment Options in Congenital Disorders of GlycosylationJulien H Park, Thorsten Marquardt
Pharmaceuticals (Basel, Switzerland)|September 28, 2023
Improved Enzyme Replacement Therapy with Cipaglucosidase Alfa/Miglustat in Infantile Pompe DiseaseLina Fiege, Ibrahim Duran, Thorsten Marquardt
The New England Journal of Medicine|May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiencyThorsten Marquardt, Eva Morava, Stephan Rust
Nutrition (Burbank, Los Angeles County, Calif.)|December 18, 2018
Long-term ketone body therapy of severe multiple acyl-CoA dehydrogenase deficiency: A case reportTobias Fischer, Ulrike Och, Thorsten Marquardt
Endocrinology, Diabetes & Metabolism Case Reports|August 16, 2023
Managing type 1 diabetes mellitus with a ketogenic dietClemens Gardemann, Sonja Knowles, Thorsten Marquardt
Brain : a Journal of Neurology|January 22, 2020
Reply: Not every excessive startle is hyperekplexia, the curious case of SOD1Julien H Park, Christiane Elpers, Thorsten Marquardt
Bioorganic & Medicinal Chemistry|November 5, 2002
Membrane-permeant derivatives of mannose-1-phosphateSynke Rutschow, Joachim Thiem, Christian Kranz, et al.
Nutrients|August 10, 2024
Influence of Carbohydrate Intake on Caprylic Acid (C8:0)-Induced Ketogenesis-A Systematic Review and Meta-AnalysisMarius Frenser, Tobias Fischer, Isabel Albrecht, et al.
Pageof 15