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The Journal of Biological Chemistry
|
April 25, 2012
Identification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymes
Wouter F Visser, Nanda M Verhoeven-Duif, Tom J de Koning
The Journal of Biological Chemistry
|
February 15, 2025
Anaplerosis by medium-chain fatty acids through complex interplay with glucose and glutamine metabolism
Hannah M German, Jolita Ciapaite, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
February 11, 2014
The potential of exosomes in diagnosis and treatment of inborn errors of metabolism
Bas W M van Balkom, Jaap van Doorn, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies
Hanneke A Haijes, Peter M van Hasselt, Judith J M Jans, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 1: Complications
Hanneke A Haijes, Judith J M Jans, Simone Y Tas, et al.
JAMA Neurology
|
December 11, 2013
Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency
Eugene F Diekman, Tom J de Koning, Nanda M Verhoeven-Duif, et al.
Human Molecular Genetics
|
July 2, 2019
Pyridox (am) ine 5'-phosphate oxidase deficiency induces seizures in Drosophila melanogaster
Wanhao Chi, Atulya S R Iyengar, Monique Albersen, et al.
Human Molecular Genetics
|
March 21, 2022
Correction to: Pyridox (am) ine 5'-phosphate oxidase deficiency induces seizures in Drosophila melanogaster
Wanhao Chi, Atulya S R Iyengar, Monique Albersen, et al.
Journal of Inherited Metabolic Disease
|
December 18, 2012
Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria
Maria Veiga-da-Cunha, Nanda M Verhoeven-Duif, Tom J de Koning, et al.
Journal of Medical Genetics
|
March 27, 2014
Expanding the clinical phenotype of COG6 deficiency
Hanneke Haijes, Hubertus C M T Prinsen, Christian Thiel, et al.
Page
of 9
Search research articles
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Showing results (1-10 of 87) with videos related to
Sort By:
Page
of 9
The Journal of Biological Chemistry
|
April 25, 2012
Identification of a human trans-3-hydroxy-L-proline dehydratase, the first characterized member of a novel family of proline racemase-like enzymes
Wouter F Visser, Nanda M Verhoeven-Duif, Tom J de Koning
The Journal of Biological Chemistry
|
February 15, 2025
Anaplerosis by medium-chain fatty acids through complex interplay with glucose and glutamine metabolism
Hannah M German, Jolita Ciapaite, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
February 11, 2014
The potential of exosomes in diagnosis and treatment of inborn errors of metabolism
Bas W M van Balkom, Jaap van Doorn, Nanda M Verhoeven-Duif, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 2: Treatment strategies
Hanneke A Haijes, Peter M van Hasselt, Judith J M Jans, et al.
Journal of Inherited Metabolic Disease
|
May 24, 2019
Pathophysiology of propionic and methylmalonic acidemias. Part 1: Complications
Hanneke A Haijes, Judith J M Jans, Simone Y Tas, et al.
JAMA Neurology
|
December 11, 2013
Survival and psychomotor development with early betaine treatment in patients with severe methylenetetrahydrofolate reductase deficiency
Eugene F Diekman, Tom J de Koning, Nanda M Verhoeven-Duif, et al.
Human Molecular Genetics
|
July 2, 2019
Pyridox (am) ine 5'-phosphate oxidase deficiency induces seizures in Drosophila melanogaster
Wanhao Chi, Atulya S R Iyengar, Monique Albersen, et al.
Human Molecular Genetics
|
March 21, 2022
Correction to: Pyridox (am) ine 5'-phosphate oxidase deficiency induces seizures in Drosophila melanogaster
Wanhao Chi, Atulya S R Iyengar, Monique Albersen, et al.
Journal of Inherited Metabolic Disease
|
December 18, 2012
Mutations in the AGXT2L2 gene cause phosphohydroxylysinuria
Maria Veiga-da-Cunha, Nanda M Verhoeven-Duif, Tom J de Koning, et al.
Journal of Medical Genetics
|
March 27, 2014
Expanding the clinical phenotype of COG6 deficiency
Hanneke Haijes, Hubertus C M T Prinsen, Christian Thiel, et al.
Page
of 9