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Joseph P Dewulf

Showing results (1-10 of 27) with videos related to

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Molecular Genetics and Metabolism|January 9, 2022
Disorders of purine biosynthesis metabolismJoseph P Dewulf, Sandrine Marie, Marie-Cécile Nassogne
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 6, 2023
Neurological presentations of inborn errors of purine and pyrimidine metabolismMarie-Cécile Nassogne, Sandrine Marie, Joseph P Dewulf
Molecular Genetics and Metabolism|February 14, 2024
DBS are suitable for 1,5-anhydroglucitol monitoring in GSD1b and G6PC3-deficient patients taking SGLT2 inhibitors to treat neutropeniaJoseph P Dewulf, Nathalie Chevalier, Sandrine Marie, et al.
Case Reports in Critical Care|August 29, 2022
Carnitine Deficiency after Long-Term Continuous Renal Replacement TherapyCaroline Van de Wyngaert, Joseph P Dewulf, Christine Collienne, et al.
British Journal of Clinical Pharmacology|February 7, 2023
Lactic acidosis after allogeneic haematopoietic stem cell transplantation potentially related to letermovirBérénice Manczak, Marie-Clémence Verdier, Joseph P Dewulf, et al.
The Journal of Biological Chemistry|August 22, 2021
ECHDC1 knockout mice accumulate ethyl-branched lipids and excrete abnormal intermediates of branched-chain fatty acid metabolismJoseph P Dewulf, Stéphanie Paquay, Etienne Marbaix, et al.
The Biochemical Journal|August 17, 2019
The synthesis of branched-chain fatty acids is limited by enzymatic decarboxylation of ethyl- and methylmalonyl-CoAJoseph P Dewulf, Isabelle Gerin, Mark H Rider, et al.
Molecular Genetics and Metabolism|January 11, 2025
Mitochondrial HMG-CoA synthase deficiencyBram Decru, Marine Lys, Kobe Truijens, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology|January 19, 2022
Unexplained Metabolic Acidosis: Alcoholic Ketoacidosis or Propylene Glycol ToxicityFanny de Landsheere, Franck Saint-Marcoux, Vincent Haufroid, et al.
Molecular Genetics and Metabolism|May 29, 2016
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patientsJoseph P Dewulf, Catherine Barrea, Marie-Françoise Vincent, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Molecular Genetics and Metabolism|January 9, 2022
Disorders of purine biosynthesis metabolismJoseph P Dewulf, Sandrine Marie, Marie-Cécile Nassogne
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 6, 2023
Neurological presentations of inborn errors of purine and pyrimidine metabolismMarie-Cécile Nassogne, Sandrine Marie, Joseph P Dewulf
Molecular Genetics and Metabolism|February 14, 2024
DBS are suitable for 1,5-anhydroglucitol monitoring in GSD1b and G6PC3-deficient patients taking SGLT2 inhibitors to treat neutropeniaJoseph P Dewulf, Nathalie Chevalier, Sandrine Marie, et al.
Case Reports in Critical Care|August 29, 2022
Carnitine Deficiency after Long-Term Continuous Renal Replacement TherapyCaroline Van de Wyngaert, Joseph P Dewulf, Christine Collienne, et al.
British Journal of Clinical Pharmacology|February 7, 2023
Lactic acidosis after allogeneic haematopoietic stem cell transplantation potentially related to letermovirBérénice Manczak, Marie-Clémence Verdier, Joseph P Dewulf, et al.
The Journal of Biological Chemistry|August 22, 2021
ECHDC1 knockout mice accumulate ethyl-branched lipids and excrete abnormal intermediates of branched-chain fatty acid metabolismJoseph P Dewulf, Stéphanie Paquay, Etienne Marbaix, et al.
The Biochemical Journal|August 17, 2019
The synthesis of branched-chain fatty acids is limited by enzymatic decarboxylation of ethyl- and methylmalonyl-CoAJoseph P Dewulf, Isabelle Gerin, Mark H Rider, et al.
Molecular Genetics and Metabolism|January 11, 2025
Mitochondrial HMG-CoA synthase deficiencyBram Decru, Marine Lys, Kobe Truijens, et al.
Journal of Medical Toxicology : Official Journal of the American College of Medical Toxicology|January 19, 2022
Unexplained Metabolic Acidosis: Alcoholic Ketoacidosis or Propylene Glycol ToxicityFanny de Landsheere, Franck Saint-Marcoux, Vincent Haufroid, et al.
Molecular Genetics and Metabolism|May 29, 2016
Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: Report on nine patientsJoseph P Dewulf, Catherine Barrea, Marie-Françoise Vincent, et al.
Pageof 3