Hibah Q. Alruwaili
Riyadh, 11211, Saudi Arabia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
Differential Changes and Biomarker Ability of Plasma Prostasin in Saudi Type 2 Diabetes Mellitus Patients: Cross-section Analysis of a Potential Protective Role and Correlation with the Disease Outcomes.
Journal: Nigerian journal of clinical practice
Published: December 25, 2025
Homozygous Loss of Function PIK3CD Mutation in Multiple Siblings Leading To B Cell Dysregulation and Autoimmunity.
Journal: Journal of clinical immunology
Published: November 04, 2024
Severe Combined Immunodeficiency from a Homozygous DNA Ligase 1 Mutant with Reduced Catalytic Activity but Increased Ligation Fidelity.
Journal: Journal of clinical immunology
Published: April 30, 2024
A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report.
Journal: Frontiers in immunology
Published: October 29, 2023
A homozygous truncating mutation of FGL2 is associated with immune dysregulation.
Journal: The Journal of allergy and clinical immunology
Published: July 06, 2022
Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia.
Journal: Journal of clinical immunology
Published: June 06, 2021
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Journal: American journal of human genetics
Published: October 05, 2019
STK4 Deficiency in a Patient with Immune Complex Glomerulonephritis, Salt-Losing Tubulopathy, and Castleman's-Like Disease.
Journal: Journal of clinical immunology
Published: April 04, 2019
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Journal: American journal of human genetics
Published: December 19, 2018
Showing 1-9 of 9
Last Updated: 09/26/2026