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H Willemsen

Showing results (101-110 of 180) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 4, 2018
Frequent Monitoring of C-Peptide Levels in Newly Diagnosed Type 1 Subjects Using Dried Blood Spots Collected at HomeRuben H Willemsen, Keith Burling, Peter Barker, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|March 12, 2022
Tooth extractions prior to chemoradiation or bioradiation are associated with weight loss during treatment for locally advanced oropharyngeal cancerDoke J M Buurman, Anna C H Willemsen, Caroline M Speksnijder, et al.
Epilepsy & Behavior : E&B|May 26, 2015
Autism and behavior in adult patients with Dravet syndrome (DS)J J L Berkvens, I Veugen, M J B M Veendrick-Meekes, et al.
Clinical Nutrition ESPEN|July 31, 2021
Malnutrition screening in head and neck cancer patients with oropharyngeal dysphagiaSorina R Simon, Walmari Pilz, Frank J P Hoebers, et al.
JIMD Reports|March 11, 2020
The c.1A > C start codon mutation in <i>CLN3</i> is associated with a protracted disease courseWillemijn F E Kuper, Claudia van Alfen, Linda van Eck, et al.
Journal of Lipid Research|January 11, 2000
Long-chain fatty acid-induced changes in gene expression in neonatal cardiac myocytesK A van der Lee, M M Vork, J E De Vries, et al.
Human Mutation|June 22, 2021
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorderFrancesca Semino, Julian Schröter, Marjolein H Willemsen, et al.
Journal of Lipid Research|November 21, 2001
Fasting-induced changes in the expression of genes controlling substrate metabolism in the rat heartK A Van der Lee, P H Willemsen, S Samec, et al.
Biophysical Journal|October 28, 1998
Simultaneous height and adhesion imaging of antibody-antigen interactions by atomic force microscopyO H Willemsen, M M Snel, K O van der Werf, et al.
Clinical Genetics|January 12, 2016
De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrumS Jansen, T Kleefstra, M H Willemsen, et al.
Pageof 18

Showing results (101-110 of 180) with videos related to

Sort By:
Pageof 18
The Journal of Clinical Endocrinology and Metabolism|June 4, 2018
Frequent Monitoring of C-Peptide Levels in Newly Diagnosed Type 1 Subjects Using Dried Blood Spots Collected at HomeRuben H Willemsen, Keith Burling, Peter Barker, et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer|March 12, 2022
Tooth extractions prior to chemoradiation or bioradiation are associated with weight loss during treatment for locally advanced oropharyngeal cancerDoke J M Buurman, Anna C H Willemsen, Caroline M Speksnijder, et al.
Epilepsy & Behavior : E&B|May 26, 2015
Autism and behavior in adult patients with Dravet syndrome (DS)J J L Berkvens, I Veugen, M J B M Veendrick-Meekes, et al.
Clinical Nutrition ESPEN|July 31, 2021
Malnutrition screening in head and neck cancer patients with oropharyngeal dysphagiaSorina R Simon, Walmari Pilz, Frank J P Hoebers, et al.
JIMD Reports|March 11, 2020
The c.1A > C start codon mutation in <i>CLN3</i> is associated with a protracted disease courseWillemijn F E Kuper, Claudia van Alfen, Linda van Eck, et al.
Journal of Lipid Research|January 11, 2000
Long-chain fatty acid-induced changes in gene expression in neonatal cardiac myocytesK A van der Lee, M M Vork, J E De Vries, et al.
Human Mutation|June 22, 2021
Further evidence for de novo variants in SYNCRIP as the cause of a neurodevelopmental disorderFrancesca Semino, Julian Schröter, Marjolein H Willemsen, et al.
Journal of Lipid Research|November 21, 2001
Fasting-induced changes in the expression of genes controlling substrate metabolism in the rat heartK A Van der Lee, P H Willemsen, S Samec, et al.
Biophysical Journal|October 28, 1998
Simultaneous height and adhesion imaging of antibody-antigen interactions by atomic force microscopyO H Willemsen, M M Snel, K O van der Werf, et al.
Clinical Genetics|January 12, 2016
De novo loss-of-function mutations in X-linked SMC1A cause severe ID and therapy-resistant epilepsy in females: expanding the phenotypic spectrumS Jansen, T Kleefstra, M H Willemsen, et al.
Pageof 18