Judith L. Meijer

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 28 publications

Health access reforms in the Caribbean Netherlands from 2010-2023.

Health access reforms in the Caribbean Netherlands from 2010-2023.

Journal: Health policy (Amsterdam, Netherlands)

Published: July 09, 2025

The Caribbean Netherlands: Health System Review.

The Caribbean Netherlands: Health System Review.

Journal: Health systems in transition

Published: March 17, 2025

Opinions on hypertension care and therapy adherence at the healthcare provider and healthcare system level: a qualitative study in the Hague, Netherlands.

Opinions on hypertension care and therapy adherence at the healthcare provider and healthcare system level: a qualitative study in the Hague, Netherlands.

Journal: BMJ open

Published: July 08, 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 Netherlands.

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 Netherlands.

Journal: International journal of environmental research and public health

Published: January 03, 2022

β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity.

β-Ureidopropionase deficiency due to novel and rare UPB1 mutations affecting pre-mRNA splicing and protein structural integrity and catalytic activity.

Journal: Molecular genetics and metabolism

Published: October 20, 2021

Children with atopic dermatitis show increased activity of β-glucocerebrosidase and stratum corneum levels of glucosylcholesterol that are strongly related to the local cytokine milieu.

Children with atopic dermatitis show increased activity of β-glucocerebrosidase and stratum corneum levels of glucosylcholesterol that are strongly related to the local cytokine milieu.

Journal: The British journal of dermatology

Published: April 27, 2021

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS.

Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS.

Journal: The New England journal of medicine

Published: April 11, 2019

Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure.

Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: August 17, 2018

Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1.

Dihydropyrimidine Dehydrogenase Deficiency: Homozygosity for an Extremely Rare Variant in DPYD due to Uniparental Isodisomy of Chromosome 1.

Journal: JIMD reports

Published: July 23, 2018

Low socioeconomic status increases effects of negative life events on antenatal anxiety and depression.

Low socioeconomic status increases effects of negative life events on antenatal anxiety and depression.

Journal: Women and birth : journal of the Australian College of Midwives

Published: March 07, 2018

Genome sequencing reveals a novel genetic mechanism underlying dihydropyrimidine dehydrogenase deficiency: A novel missense variant c.1700G>A and a large intragenic inversion in DPYD spanning intron 8 to intron 12.

Genome sequencing reveals a novel genetic mechanism underlying dihydropyrimidine dehydrogenase deficiency: A novel missense variant c.1700G>A and a large intragenic inversion in DPYD spanning intron 8 to intron 12.

Journal: Human mutation

Published: December 04, 2017

Dihydropyrimidinase deficiency in four East Asian patients due to novel and rare DPYS mutations affecting protein structural integrity and catalytic activity.

Dihydropyrimidinase deficiency in four East Asian patients due to novel and rare DPYS mutations affecting protein structural integrity and catalytic activity.

Journal: Molecular genetics and metabolism

Published: September 05, 2017

Showing 1-12 of 28

Last Updated: 09/26/2026