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Josanne Cox-Brinkman

Showing results (1-10 of 6) with videos related to

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European Journal of Human Genetics : EJHG|March 1, 2007
Three-dimensional face shape in Fabry diseaseJosanne Cox-Brinkman, Anouk Vedder, Carla Hollak, et al.
Ultrastructural Pathology|May 12, 2010
Ultrastructural analysis of dermal fibroblasts in mucopolysaccharidosis type I: Effects of enzyme replacement therapy and hematopoietic cell transplantationJosanne Cox-Brinkman, Marius A van den Bergh Weerman, Frits A Wijburg, et al.
Molecular Genetics and Metabolism|November 21, 2007
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry diseaseChristiane Auray-Blais, Denis Cyr, Aimé Ntwari, et al.
BMJ Global Health|May 31, 2023
Structural under-reporting of informed consent, data handling and sharing, ethical approval, and application of Open Science principles as proxies for study quality conduct in COVID-19 research: a systematic scoping reviewNick Wilmes, Charlotte W E Hendriks, Caspar T A Viets, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2008
Elevated globotriaosylsphingosine is a hallmark of Fabry diseaseJohannes M Aerts, Johanna E Groener, Sijmen Kuiper, et al.
Journal of Inherited Metabolic Disease|March 30, 2011
Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodiesJohannes M F G Aerts, Wouter W Kallemeijn, Wouter Wegdam, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|March 1, 2007
Three-dimensional face shape in Fabry diseaseJosanne Cox-Brinkman, Anouk Vedder, Carla Hollak, et al.
Ultrastructural Pathology|May 12, 2010
Ultrastructural analysis of dermal fibroblasts in mucopolysaccharidosis type I: Effects of enzyme replacement therapy and hematopoietic cell transplantationJosanne Cox-Brinkman, Marius A van den Bergh Weerman, Frits A Wijburg, et al.
Molecular Genetics and Metabolism|November 21, 2007
Urinary globotriaosylceramide excretion correlates with the genotype in children and adults with Fabry diseaseChristiane Auray-Blais, Denis Cyr, Aimé Ntwari, et al.
BMJ Global Health|May 31, 2023
Structural under-reporting of informed consent, data handling and sharing, ethical approval, and application of Open Science principles as proxies for study quality conduct in COVID-19 research: a systematic scoping reviewNick Wilmes, Charlotte W E Hendriks, Caspar T A Viets, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 22, 2008
Elevated globotriaosylsphingosine is a hallmark of Fabry diseaseJohannes M Aerts, Johanna E Groener, Sijmen Kuiper, et al.
Journal of Inherited Metabolic Disease|March 30, 2011
Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodiesJohannes M F G Aerts, Wouter W Kallemeijn, Wouter Wegdam, et al.
Pageof 1