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K van Dijk

Showing results (81-90 of 93) with videos related to

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BMC Genomics|March 19, 2013
Genome-wide analysis of macrosatellite repeat copy number variation in worldwide populations: evidence for differences and commonalities in size distributions and size restrictionsMireille Schaap, Richard J L F Lemmers, Roel Maassen, et al.
Expert Review of Pharmacoeconomics & Outcomes Research|December 13, 2025
Economic evaluation of an add-on module to reduce intrusive suicidal mental images in patients with depressive symptomsJaël van Bentum, Ben Wijnen, Nathan Bachrach, et al.
Gene|October 21, 2022
SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnosticsMohamed Z Alimohamed, Ludolf G Boven, Krista K van Dijk, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 6, 2026
High-oxalate diet-induced kidney injury impairs AVF remodeling via hypertension, endothelial damage, and immune activationE P de Winter, N Kruit, K van Dijk, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
Frontiers in Genetics|April 11, 2022
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown SignificanceFatemeh Ghorbani, Mohamed Z Alimohamed, Juliana F Vilacha, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
BMC Medical Genomics|February 6, 2016
Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephalyPatrick Rump, Omid Jazayeri, Krista K van Dijk-Bos, et al.
Journal of Consulting and Clinical Psychology|July 18, 2024
Reducing intrusive suicidal mental images in patients with depressive symptoms through a dual-task add-on module: Results of a multicenter randomized clinical trialJaël S van Bentum, Marit Sijbrandij, Ad J F M Kerkhof, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|June 14, 2021
Improvement in left ventricular ejection fraction after pharmacological up-titration in new-onset heart failure with reduced ejection fractionJ F Nauta, B T Santema, M H L van der Wal, et al.
Pageof 10

Showing results (81-90 of 93) with videos related to

Sort By:
Pageof 10
BMC Genomics|March 19, 2013
Genome-wide analysis of macrosatellite repeat copy number variation in worldwide populations: evidence for differences and commonalities in size distributions and size restrictionsMireille Schaap, Richard J L F Lemmers, Roel Maassen, et al.
Expert Review of Pharmacoeconomics & Outcomes Research|December 13, 2025
Economic evaluation of an add-on module to reduce intrusive suicidal mental images in patients with depressive symptomsJaël van Bentum, Ben Wijnen, Nathan Bachrach, et al.
Gene|October 21, 2022
SEPT-GD: A decision tree to prioritise potential RNA splice variants in cardiomyopathy genes for functional splicing assays in diagnosticsMohamed Z Alimohamed, Ludolf G Boven, Krista K van Dijk, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 6, 2026
High-oxalate diet-induced kidney injury impairs AVF remodeling via hypertension, endothelial damage, and immune activationE P de Winter, N Kruit, K van Dijk, et al.
Human Mutation|February 12, 2016
CoNVaDING: Single Exon Variation Detection in Targeted NGS DataLennart F Johansson, Freerk van Dijk, Eddy N de Boer, et al.
Frontiers in Genetics|April 11, 2022
Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown SignificanceFatemeh Ghorbani, Mohamed Z Alimohamed, Juliana F Vilacha, et al.
International Journal of Cardiology|March 4, 2021
Diagnostic yield of targeted next generation sequencing in 2002 Dutch cardiomyopathy patientsMohamed Z Alimohamed, Lennart F Johansson, Anna Posafalvi, et al.
BMC Medical Genomics|February 6, 2016
Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephalyPatrick Rump, Omid Jazayeri, Krista K van Dijk-Bos, et al.
Journal of Consulting and Clinical Psychology|July 18, 2024
Reducing intrusive suicidal mental images in patients with depressive symptoms through a dual-task add-on module: Results of a multicenter randomized clinical trialJaël S van Bentum, Marit Sijbrandij, Ad J F M Kerkhof, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|June 14, 2021
Improvement in left ventricular ejection fraction after pharmacological up-titration in new-onset heart failure with reduced ejection fractionJ F Nauta, B T Santema, M H L van der Wal, et al.
Pageof 10