Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Judith Meijer

Showing results (1-10 of 31) with videos related to

Pageof 4
Sort By:
International Journal of Environmental Research and Public Health|February 25, 2022
The Use of the Bolk Model for Positive Health and Living Environment in the Development of an Integrated Health Promotion Approach: A Case Study in a Socioeconomically Deprived Neighborhood in The NetherlandsHerman A van Wietmarschen, Sjef Staps, Judith Meijer, et al.
JIMD Reports|May 14, 2015
Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated DonorNicholas Brodszki, Maria Svensson, André B P van Kuilenburg, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2012
Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomyJoyce Geelen, Rolph Pfundt, Judith Meijer, et al.
Molecular Syndromology|January 8, 2015
Dihydropyrimidine dehydrogenase deficiency in two malaysian siblings with abnormal MRI findingsBee Chin Chen, Rowani Mohd Rawi, Rutger Meinsma, et al.
International Journal of Molecular Sciences|January 16, 2016
Altered Pre-mRNA Splicing Caused by a Novel Intronic Mutation c.1443+5G>A in the Dihydropyrimidinase (DPYS) GeneYoko Nakajima, Judith Meijer, Chunhua Zhang, et al.
Molecular Pharmacology|August 3, 2013
Role of human hypoxanthine guanine phosphoribosyltransferase in activation of the antiviral agent T-705 (favipiravir)Lieve Naesens, Luke W Guddat, Dianne T Keough, et al.
Acta Biochimica Polonica|December 17, 2008
Dihydropyrimidine dehydrogenase deficiency presenting with psychomotor retardation in the first Polish patientArtur Mazur, Szymon Figurski, Anna Płoskoń, et al.
JIMD Reports|October 24, 2018
Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1André B P van Kuilenburg, Judith Meijer, Rutger Meinsma, et al.
Health Policy (Amsterdam, Netherlands)|December 13, 2025
Health access reforms in the Caribbean Netherlands from 2010-2023Nathan Shuftan, Jane O'Flynn, Judith Meijer, et al.
Health Systems in Transition|March 17, 2025
The Caribbean Netherlands: Health System ReviewNathan Shuftan, Jane O'Flynn, Judith Meijer, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
International Journal of Environmental Research and Public Health|February 25, 2022
The Use of the Bolk Model for Positive Health and Living Environment in the Development of an Integrated Health Promotion Approach: A Case Study in a Socioeconomically Deprived Neighborhood in The NetherlandsHerman A van Wietmarschen, Sjef Staps, Judith Meijer, et al.
JIMD Reports|May 14, 2015
Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated DonorNicholas Brodszki, Maria Svensson, André B P van Kuilenburg, et al.
The Journal of Allergy and Clinical Immunology|December 25, 2012
Severe phenotype of severe combined immunodeficiency caused by adenosine deaminase deficiency in a patient with a homozygous mutation due to uniparental disomyJoyce Geelen, Rolph Pfundt, Judith Meijer, et al.
Molecular Syndromology|January 8, 2015
Dihydropyrimidine dehydrogenase deficiency in two malaysian siblings with abnormal MRI findingsBee Chin Chen, Rowani Mohd Rawi, Rutger Meinsma, et al.
International Journal of Molecular Sciences|January 16, 2016
Altered Pre-mRNA Splicing Caused by a Novel Intronic Mutation c.1443+5G>A in the Dihydropyrimidinase (DPYS) GeneYoko Nakajima, Judith Meijer, Chunhua Zhang, et al.
Molecular Pharmacology|August 3, 2013
Role of human hypoxanthine guanine phosphoribosyltransferase in activation of the antiviral agent T-705 (favipiravir)Lieve Naesens, Luke W Guddat, Dianne T Keough, et al.
Acta Biochimica Polonica|December 17, 2008
Dihydropyrimidine dehydrogenase deficiency presenting with psychomotor retardation in the first Polish patientArtur Mazur, Szymon Figurski, Anna Płoskoń, et al.
JIMD Reports|October 24, 2018
Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1André B P van Kuilenburg, Judith Meijer, Rutger Meinsma, et al.
Health Policy (Amsterdam, Netherlands)|December 13, 2025
Health access reforms in the Caribbean Netherlands from 2010-2023Nathan Shuftan, Jane O'Flynn, Judith Meijer, et al.
Health Systems in Transition|March 17, 2025
The Caribbean Netherlands: Health System ReviewNathan Shuftan, Jane O'Flynn, Judith Meijer, et al.
Pageof 4