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J Derks

Showing results (141-150 of 167) with videos related to

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Molecular Genetics and Metabolism|January 26, 2024
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshopSarah C Grünert, Terry G J Derks, Helen Mundy, et al.
JACC. Basic to Translational Science|May 4, 2023
Clustering of Cardiac Transcriptome Profiles Reveals Unique: Subgroups of Dilated Cardiomyopathy PatientsJob A J Verdonschot, Ping Wang, Kasper W J Derks, et al.
Orphanet Journal of Rare Diseases|May 29, 2012
Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort studyCatharina M L Touw, G Peter A Smit, Maaike de Vries, et al.
Scientific Reports|September 24, 2021
Non-invasively measured brain activity and radiological progression in diffuse gliomaT Numan, S D Kulik, B Moraal, et al.
Lung Cancer (Amsterdam, Netherlands)|August 1, 2025
Definition of resectable stage III non-small cell lung cancer: A systematic review from EORTC lung cancer groupE Xenophontos, N Giaj Levra, V Durieux, et al.
European Heart Journal|November 6, 2020
Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differencesJob A J Verdonschot, Marco Merlo, Fernando Dominguez, et al.
Journal of Inherited Metabolic Disease|March 19, 2021
Impaired Very-Low-Density Lipoprotein catabolism links hypoglycemia to hypertriglyceridemia in Glycogen Storage Disease type IaJoanne A Hoogerland, Fabian Peeks, Brenda S Hijmans, et al.
Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.
European Heart Journal|January 30, 2018
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-term life-threatening arrhythmiasJob A J Verdonschot, Mark R Hazebroek, Kasper W J Derks, et al.
Molecular Genetics and Metabolism|July 11, 2017
Clinical presentation and outcome in a series of 32 patients with 2-methylacetoacetyl-coenzyme A thiolase (MAT) deficiencySarah Catharina Grünert, Robert Niklas Schmitt, Sonja Marina Schlatter, et al.
Pageof 17

Showing results (141-150 of 167) with videos related to

Sort By:
Pageof 17
Molecular Genetics and Metabolism|January 26, 2024
Treatment recommendations for glycogen storage disease type IB- associated neutropenia and neutrophil dysfunction with empagliflozin: Consensus from an international workshopSarah C Grünert, Terry G J Derks, Helen Mundy, et al.
JACC. Basic to Translational Science|May 4, 2023
Clustering of Cardiac Transcriptome Profiles Reveals Unique: Subgroups of Dilated Cardiomyopathy PatientsJob A J Verdonschot, Ping Wang, Kasper W J Derks, et al.
Orphanet Journal of Rare Diseases|May 29, 2012
Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort studyCatharina M L Touw, G Peter A Smit, Maaike de Vries, et al.
Scientific Reports|September 24, 2021
Non-invasively measured brain activity and radiological progression in diffuse gliomaT Numan, S D Kulik, B Moraal, et al.
Lung Cancer (Amsterdam, Netherlands)|August 1, 2025
Definition of resectable stage III non-small cell lung cancer: A systematic review from EORTC lung cancer groupE Xenophontos, N Giaj Levra, V Durieux, et al.
European Heart Journal|November 6, 2020
Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differencesJob A J Verdonschot, Marco Merlo, Fernando Dominguez, et al.
Journal of Inherited Metabolic Disease|March 19, 2021
Impaired Very-Low-Density Lipoprotein catabolism links hypoglycemia to hypertriglyceridemia in Glycogen Storage Disease type IaJoanne A Hoogerland, Fabian Peeks, Brenda S Hijmans, et al.
Orphanet Journal of Rare Diseases|May 19, 2016
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsC I van Capelle, J C van der Meijden, J M P van den Hout, et al.
European Heart Journal|January 30, 2018
Titin cardiomyopathy leads to altered mitochondrial energetics, increased fibrosis and long-term life-threatening arrhythmiasJob A J Verdonschot, Mark R Hazebroek, Kasper W J Derks, et al.
Molecular Genetics and Metabolism|July 11, 2017
Clinical presentation and outcome in a series of 32 patients with 2-methylacetoacetyl-coenzyme A thiolase (MAT) deficiencySarah Catharina Grünert, Robert Niklas Schmitt, Sonja Marina Schlatter, et al.
Pageof 17