Mofareh S. Alzahrani

Riyadh, 11525, Saudi Arabia

Last Updated: 09/26/2026

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Found 12 publications

A Novel Variant of CORO1A Gene Contributing to the Development of Primary Immunodeficiency in Children.

A Novel Variant of CORO1A Gene Contributing to the Development of Primary Immunodeficiency in Children.

Journal: Case reports in immunology

Published: February 05, 2026

Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysis.

Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysis.

Journal: Clinical immunology (Orlando, Fla.)

Published: June 11, 2024

Hematopoietic Stem Cell Transplantation Corrects IL-2Rβ Deficiency.

Hematopoietic Stem Cell Transplantation Corrects IL-2Rβ Deficiency.

Journal: Journal of clinical immunology

Published: May 30, 2024

Clinical Presentation and Management of Multisystem Inflammatory Syndrome in Children With COVID-19: A Systematic Review.

Clinical Presentation and Management of Multisystem Inflammatory Syndrome in Children With COVID-19: A Systematic Review.

Journal: Cureus

Published: October 12, 2023

The Effect of Food Allergen Exclusion on the Growth of Saudi Children.

The Effect of Food Allergen Exclusion on the Growth of Saudi Children.

Journal: Children (Basel, Switzerland)

Published: July 07, 2023

Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB.

Multiple Family Members With Delayed Cord Separtion and Combined Immunodeficiency With Novel Mutation in IKBKB.

Journal: Frontiers in pediatrics

Published: October 14, 2019

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.

Journal: Genome medicine

Published: January 10, 2019

Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features.

Three Types of Immunodeficiency, Centromeric Instability, and Facial Anomalies (ICF) Syndrome Identified by Whole-Exome Sequencing in Saudi Hypogammaglobulinemia Patients: Clinical, Molecular, and Cytogenetic Features.

Journal: Journal of clinical immunology

Published: April 30, 2018

Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.

Mendelian Susceptibility to Mycobacterial Disease Caused by a Novel Founder IL12B Mutation in Saudi Arabia.

Journal: Journal of clinical immunology

Published: December 07, 2017

Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation.

Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation.

Journal: Science (New York, N.Y.)

Published: October 24, 2017

A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations.

A digenic human immunodeficiency characterized by IFNAR1 and IFNGR2 mutations.

Journal: The Journal of clinical investigation

Published: February 17, 2017

Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing.

Identification of a novel SBF2 missense mutation associated with a rare case of thrombocytopenia using whole-exome sequencing.

Journal: Journal of thrombosis and thrombolysis

Published: January 22, 2013

Showing 1-12 of 12

Last Updated: 09/26/2026