Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Iranian Journal of Allergy, Asthma, and Immunology
|
November 20, 2025
Diverse Phenotypic Expressions of ADA2 Deficiency: Two Case Studies
Anahita Razaghian, Zahra Alizadeh, Isabelle Meyts, et al.
Current Allergy and Asthma Reports
|
July 6, 2024
Human ADA2 Deficiency: Ten Years Later
Marjon Wouters, Lisa Ehlers, Mariia Dzhus, et al.
The Journal of Clinical Investigation
|
January 2, 2026
Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function
Jarne Beliën, Amber De Visscher, Bethany Pillay, et al.
Journal of Clinical Immunology
|
August 7, 2023
A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency
Mariia Dzhus, Lisa Ehlers, Marjon Wouters, et al.
Clinical Immunology (Orlando, Fla.)
|
March 1, 2026
Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease
Willem Roosens, Marjon Wouters, Frederik Staels, et al.
Journal of Human Immunity
|
July 1, 2026
Two novel kindreds with autosomal recessive STAT2 deficiency
Verena Kienapfel, Lotte Cresens, Lucy Bizien, et al.
The Journal of Experimental Medicine
|
January 9, 2026
Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
The Journal of Experimental Medicine
|
August 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Cell Death Discovery
|
March 23, 2026
ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances
Lisa Ehlers, Marjon Wouters, Bethany Pillay, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 23, 2024
Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Iranian Journal of Allergy, Asthma, and Immunology
|
November 20, 2025
Diverse Phenotypic Expressions of ADA2 Deficiency: Two Case Studies
Anahita Razaghian, Zahra Alizadeh, Isabelle Meyts, et al.
Current Allergy and Asthma Reports
|
July 6, 2024
Human ADA2 Deficiency: Ten Years Later
Marjon Wouters, Lisa Ehlers, Mariia Dzhus, et al.
The Journal of Clinical Investigation
|
January 2, 2026
Human adenosine deaminase type 2 deficiency enhances NK cell activation but impairs maturation and function
Jarne Beliën, Amber De Visscher, Bethany Pillay, et al.
Journal of Clinical Immunology
|
August 7, 2023
A Narrative Review of the Neurological Manifestations of Human Adenosine Deaminase 2 Deficiency
Mariia Dzhus, Lisa Ehlers, Marjon Wouters, et al.
Clinical Immunology (Orlando, Fla.)
|
March 1, 2026
Identification of a novel hypomorphic variant in CYBB underlying an adult presentation of X-linked recessive Mendelian susceptibility to mycobacterial disease
Willem Roosens, Marjon Wouters, Frederik Staels, et al.
Journal of Human Immunity
|
July 1, 2026
Two novel kindreds with autosomal recessive STAT2 deficiency
Verena Kienapfel, Lotte Cresens, Lucy Bizien, et al.
The Journal of Experimental Medicine
|
January 9, 2026
Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
The Journal of Experimental Medicine
|
August 27, 2025
Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Cell Death Discovery
|
March 23, 2026
ADA2-deficient cells exhibit increased levels of cell death and metabolic disturbances
Lisa Ehlers, Marjon Wouters, Bethany Pillay, et al.
Medrxiv : the Preprint Server for Health Sciences
|
December 23, 2024
Dominant negative <i>ADA2</i> mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, et al.
Page
of 2