Amel S. Hassan

Doha, DA, Qatar

Last Updated: 09/26/2026

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Found 13 publications

Inherited human TFIIIA deficiency disrupts T cell development.

Inherited human TFIIIA deficiency disrupts T cell development.

Journal: medRxiv : the preprint server for health sciences

Published: July 10, 2026

Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.

Dual variants of uncertain significance in a case of hyper-IgM syndrome: implications for diagnosis and management.

Journal: Frontiers in immunology

Published: March 16, 2025

Novel Synonymous Variant in IL7R Causes Preferential Expression of the Soluble Isoform.

Novel Synonymous Variant in IL7R Causes Preferential Expression of the Soluble Isoform.

Journal: Journal of clinical immunology

Published: August 28, 2023

Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration.

Loss of the TRPM4 channel in humans causes immune dysregulation with defective monocyte migration.

Journal: The Journal of allergy and clinical immunology

Published: June 07, 2023

Case report: Neonatal autoimmune lymphoproliferative syndrome with a novel pathogenic homozygous FAS variant effectively treated with sirolimus.

Case report: Neonatal autoimmune lymphoproliferative syndrome with a novel pathogenic homozygous FAS variant effectively treated with sirolimus.

Journal: Frontiers in pediatrics

Published: January 23, 2023

A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes.

A Novel STK4 Mutation Impairs T Cell Immunity Through Dysregulation of Cytokine-Induced Adhesion and Chemotaxis Genes.

Journal: Journal of clinical immunology

Published: March 14, 2021

Novel ORAI1 Mutation Disrupts Channel Trafficking Resulting in Combined Immunodeficiency.

Novel ORAI1 Mutation Disrupts Channel Trafficking Resulting in Combined Immunodeficiency.

Journal: Journal of clinical immunology

Published: November 30, 2020

X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.

X-Linked Agammaglobulinemia Case with TH Domain Missense Mutation in Bruton Tyrosine Kinase.

Journal: Journal of clinical immunology

Published: July 21, 2020

Willingness to participate in genome testing: a survey of public attitudes from Qatar.

Willingness to participate in genome testing: a survey of public attitudes from Qatar.

Journal: Journal of human genetics

Published: January 23, 2020

Symptomatic males and female carriers in a large Caucasian kindred with XIAP deficiency.

Symptomatic males and female carriers in a large Caucasian kindred with XIAP deficiency.

Journal: Journal of clinical immunology

Published: September 30, 2014

Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency.

Comparison of outcomes of hematopoietic stem cell transplantation without chemotherapy conditioning by using matched sibling and unrelated donors for treatment of severe combined immunodeficiency.

Journal: The Journal of allergy and clinical immunology

Published: February 20, 2014

Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency.

Host natural killer immunity is a key indicator of permissiveness for donor cell engraftment in patients with severe combined immunodeficiency.

Journal: The Journal of allergy and clinical immunology

Published: August 19, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026