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Nature Medicine
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May 4, 2004
A COG in the sugar machine
Thorsten 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 Glycosylation
Julien H Park, Thorsten Marquardt
Pharmaceuticals (Basel, Switzerland)
|
September 28, 2023
Improved Enzyme Replacement Therapy with Cipaglucosidase Alfa/Miglustat in Infantile Pompe Disease
Lina Fiege, Ibrahim Duran, Thorsten Marquardt
The New England Journal of Medicine
|
May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiency
Thorsten 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 report
Tobias Fischer, Ulrike Och, Thorsten Marquardt
Endocrinology, Diabetes & Metabolism Case Reports
|
August 16, 2023
Managing type 1 diabetes mellitus with a ketogenic diet
Clemens Gardemann, Sonja Knowles, Thorsten Marquardt
Brain : a Journal of Neurology
|
January 22, 2020
Reply: Not every excessive startle is hyperekplexia, the curious case of SOD1
Julien H Park, Christiane Elpers, Thorsten Marquardt
Bioorganic & Medicinal Chemistry
|
November 5, 2002
Membrane-permeant derivatives of mannose-1-phosphate
Synke 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-Analysis
Marius Frenser, Tobias Fischer, Isabel Albrecht, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 142) with videos related to
Sort By:
Page
of 15
Nature Medicine
|
May 4, 2004
A COG in the sugar machine
Thorsten 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 Glycosylation
Julien H Park, Thorsten Marquardt
Pharmaceuticals (Basel, Switzerland)
|
September 28, 2023
Improved Enzyme Replacement Therapy with Cipaglucosidase Alfa/Miglustat in Infantile Pompe Disease
Lina Fiege, Ibrahim Duran, Thorsten Marquardt
The New England Journal of Medicine
|
May 23, 2014
Multiple phenotypes in phosphoglucomutase 1 deficiency
Thorsten 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 report
Tobias Fischer, Ulrike Och, Thorsten Marquardt
Endocrinology, Diabetes & Metabolism Case Reports
|
August 16, 2023
Managing type 1 diabetes mellitus with a ketogenic diet
Clemens Gardemann, Sonja Knowles, Thorsten Marquardt
Brain : a Journal of Neurology
|
January 22, 2020
Reply: Not every excessive startle is hyperekplexia, the curious case of SOD1
Julien H Park, Christiane Elpers, Thorsten Marquardt
Bioorganic & Medicinal Chemistry
|
November 5, 2002
Membrane-permeant derivatives of mannose-1-phosphate
Synke 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-Analysis
Marius Frenser, Tobias Fischer, Isabel Albrecht, et al.
Page
of 15