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Marc Engelen

Showing results (111-120 of 137) with videos related to

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Stroke|February 22, 2021
Endovascular Treatment for Acute Ischemic Stroke in Children: Experience From the MR CLEAN RegistryAdriaan C G M van Es, Maayke A W Hunfeld, Ido van den Wijngaard, et al.
Journal of Inherited Metabolic Disease|July 30, 2016
Cholic acid therapy in Zellweger spectrum disordersKevin Berendse, Femke C C Klouwer, Bart G P Koot, et al.
Journal of Inherited Metabolic Disease|February 23, 2019
The cholic acid extension study in Zellweger spectrum disorders: Results and implications for therapyFemke C C Klouwer, Bart G P Koot, Kevin Berendse, et al.
The Journal of Clinical Investigation|March 10, 2021
Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophyQuentin Raas, Malu-Clair van de Beek, Sonja Forss-Petter, et al.
Communications Medicine|September 10, 2024
Lipidomic biomarkers in plasma correlate with disease severity in adrenoleukodystrophyYorrick R J Jaspers, Hemmo A F Yska, Caroline G Bergner, et al.
The Lancet. Neurology|January 21, 2023
Safety and efficacy of leriglitazone for preventing disease progression in men with adrenomyeloneuropathy (ADVANCE): a randomised, double-blind, multi-centre, placebo-controlled phase 2-3 trialWolfgang Köhler, Marc Engelen, Florian Eichler, et al.
Journal of Inherited Metabolic Disease|July 2, 2024
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deteriorationNicole Hammann, Dominic Lenz, Alyssa Bianzano, et al.
Genes|December 24, 2021
Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the <i>ABCD1</i> GeneStephanie I W van de Stadt, Petra A W Mooyer, Inge M E Dijkstra, et al.
Journal of Inherited Metabolic Disease|February 9, 2026
The Grey Zone Project: Risk-Based Classification of ABCD1 Variants in X-Linked AdrenoleukodystrophyTroy C Lund, Kelly Miettunen, Yorrick R J Jaspers, et al.
Frontiers in Physiology|January 10, 2022
<i>STXBP1</i> Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Pageof 14

Showing results (111-120 of 137) with videos related to

Sort By:
Pageof 14
Stroke|February 22, 2021
Endovascular Treatment for Acute Ischemic Stroke in Children: Experience From the MR CLEAN RegistryAdriaan C G M van Es, Maayke A W Hunfeld, Ido van den Wijngaard, et al.
Journal of Inherited Metabolic Disease|July 30, 2016
Cholic acid therapy in Zellweger spectrum disordersKevin Berendse, Femke C C Klouwer, Bart G P Koot, et al.
Journal of Inherited Metabolic Disease|February 23, 2019
The cholic acid extension study in Zellweger spectrum disorders: Results and implications for therapyFemke C C Klouwer, Bart G P Koot, Kevin Berendse, et al.
The Journal of Clinical Investigation|March 10, 2021
Metabolic rerouting via SCD1 induction impacts X-linked adrenoleukodystrophyQuentin Raas, Malu-Clair van de Beek, Sonja Forss-Petter, et al.
Communications Medicine|September 10, 2024
Lipidomic biomarkers in plasma correlate with disease severity in adrenoleukodystrophyYorrick R J Jaspers, Hemmo A F Yska, Caroline G Bergner, et al.
The Lancet. Neurology|January 21, 2023
Safety and efficacy of leriglitazone for preventing disease progression in men with adrenomyeloneuropathy (ADVANCE): a randomised, double-blind, multi-centre, placebo-controlled phase 2-3 trialWolfgang Köhler, Marc Engelen, Florian Eichler, et al.
Journal of Inherited Metabolic Disease|July 2, 2024
MRI in LARS1 deficiency-Spectrum, patterns, and correlation with acute neurological deteriorationNicole Hammann, Dominic Lenz, Alyssa Bianzano, et al.
Genes|December 24, 2021
Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the <i>ABCD1</i> GeneStephanie I W van de Stadt, Petra A W Mooyer, Inge M E Dijkstra, et al.
Journal of Inherited Metabolic Disease|February 9, 2026
The Grey Zone Project: Risk-Based Classification of ABCD1 Variants in X-Linked AdrenoleukodystrophyTroy C Lund, Kelly Miettunen, Yorrick R J Jaspers, et al.
Frontiers in Physiology|January 10, 2022
<i>STXBP1</i> Syndrome Is Characterized by Inhibition-Dominated Dynamics of Resting-State EEGSimon J Houtman, Hanna C A Lammertse, Annemiek A van Berkel, et al.
Pageof 14