Marjon Wouters

Leuven, VLG, Belgium

Last Updated: 09/26/2026

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Found 13 publications

Two novel kindreds with autosomal recessive STAT2 deficiency.

Two novel kindreds with autosomal recessive STAT2 deficiency.

Journal: Journal of human immunity
Published: March 04, 2026

Adenosine deaminase type 2 deficiency: From rare to common.

Adenosine deaminase type 2 deficiency: From rare to common.

Journal: Journal of human immunity
Published: January 27, 2026

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease.

Journal: Clinical immunology (Orlando, Fla.)
Published: January 16, 2026

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: The Journal of experimental medicine
Published: January 09, 2026

Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function.

Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function.

Journal: The Journal of clinical investigation
Published: January 02, 2026

ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances.

Journal: Cell death discovery
Published: August 02, 2025

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: The Journal of experimental medicine
Published: March 05, 2025

Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes.

Inhibition of lysosomal degradation increases expression of mutant ADA2 in DADA2 monocytes.

Journal: The Journal of allergy and clinical immunology
Published: February 17, 2025

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers.

Journal: medRxiv : the preprint server for health sciences
Published: December 23, 2024

Diverse Phenotypic Expressions of ADA2 Deficiency: Two Case Studies.

Diverse Phenotypic Expressions of ADA2 Deficiency: Two Case Studies.

Journal: Iranian journal of allergy, asthma, and immunology
Published: October 24, 2024

Human ADA2 Deficiency: Ten Years Later.

Human ADA2 Deficiency: Ten Years Later.

Journal: Current allergy and asthma reports
Published: June 26, 2024

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Human Autosomal Recessive DNA Polymerase Delta 3 Deficiency Presenting as Omenn Syndrome.

Journal: Journal of clinical immunology
Published: October 06, 2023
Showing 1-12 of 13

Last Updated: 09/26/2026