Marcel Van Deuren
Nijmegen, GE, Netherlands
Last Updated: 09/26/2026
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Found 59 publications
Genetic determinants of the complement and coagulation pathways in invasive meningococcal disease.
Journal: The Journal of allergy and clinical immunology
Published: March 28, 2025
Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity: A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers.
Journal: Frontiers in immunology
Published: September 20, 2021
Differences in local immune cell landscape between Q fever and atherosclerotic abdominal aortic aneurysms identified by multiplex immunohistochemistry.
Journal: eLife
Published: July 26, 2021
Complement factor D haplodeficiency is associated with a reduced complement activation speed and diminished bacterial killing.
Journal: Clinical & translational immunology
Published: November 15, 2020
Dysregulated Innate and Adaptive Immune Responses Discriminate Disease Severity in COVID-19.
Journal: The Journal of infectious diseases
Published: October 21, 2020
Considerations for radiotherapy in Bloom Syndrome: A case series.
Journal: European journal of medical genetics
Published: September 08, 2020
Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency.
Journal: Journal of clinical immunology
Published: April 30, 2020
Kallikrein-kinin blockade in patients with COVID-19 to prevent acute respiratory distress syndrome.
Journal: eLife
Published: April 09, 2020
Single nucleotide polymorphism (SNP) rs3751143 in P2RX7 is associated with therapy failure in chronic Q fever while rs7125062 in MMP1 is associated with fewer complications.
Journal: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
Published: February 10, 2020
Classic ataxia-telangiectasia: the phenotype of long-term survivors.
Journal: Journal of neurology
Published: September 17, 2019
Phenotypic variability including Behçet's disease-like manifestations in DADA2 patients due to a homozygous c.973-2A>G splice site mutation.
Journal: Clinical and experimental rheumatology
Published: August 04, 2019
Plasma therapy leads to an increase in functional IgA and IgM concentration in the blood and saliva of a patient with X-linked agammaglobulinemia.
Journal: Journal of translational medicine
Published: February 14, 2019
Last Updated: 09/26/2026