Mohammad S. Ehlayel

Doha, DA, Qatar

Last Updated: 09/26/2026

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Found 14 publications

Human PLCG2 haploinsufficiency results in a novel natural killer cell immunodeficiency.

Human PLCG2 haploinsufficiency results in a novel natural killer cell immunodeficiency.

Journal: The Journal of allergy and clinical immunology

Published: February 13, 2023

Sensitization to Common Allergens Among Children with Asthma and Allergic Rhinitis in Qatar.

Sensitization to Common Allergens Among Children with Asthma and Allergic Rhinitis in Qatar.

Journal: Journal of asthma and allergy

Published: December 02, 2020

A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families.

A founder RAB27A variant causes Griscelli syndrome type 2 with phenotypic heterogeneity in Qatari families.

Journal: American journal of medical genetics. Part A

Published: May 19, 2020

Risk factors of zinc deficiency in children with atopic dermatitis.

Risk factors of zinc deficiency in children with atopic dermatitis.

Journal: European annals of allergy and clinical immunology

Published: October 09, 2019

Camel's milk allergy.

Camel's milk allergy.

Journal: Allergy and asthma proceedings

Published: August 30, 2018

Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies.

Biallelic mutations in DNA ligase 1 underlie a spectrum of immune deficiencies.

Journal: The Journal of clinical investigation

Published: January 23, 2018

Allergic diseases among children: nutritional prevention and intervention.

Allergic diseases among children: nutritional prevention and intervention.

Journal: Therapeutics and clinical risk management

Published: March 30, 2016

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders.

Journal: The Journal of allergy and clinical immunology

Published: February 02, 2016

A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism.

A novel Rab27a mutation binds melanophilin, but not Munc13-4, causing immunodeficiency without albinism.

Journal: The Journal of allergy and clinical immunology

Published: June 01, 2015

Non-truncating LIFR mutation: causal for prominent congenital pain insensitivity phenotype with progressive vertebral destruction?

Non-truncating LIFR mutation: causal for prominent congenital pain insensitivity phenotype with progressive vertebral destruction?

Journal: Clinical genetics

Published: April 15, 2015

Linear growth and endocrine function in children with ataxia telangiectasia.

Linear growth and endocrine function in children with ataxia telangiectasia.

Journal: Indian journal of endocrinology and metabolism

Published: December 25, 2014

The impact of Vitamin D deficiency on asthma, allergic rhinitis and wheezing in children: An emerging public health problem.

The impact of Vitamin D deficiency on asthma, allergic rhinitis and wheezing in children: An emerging public health problem.

Journal: Journal of family & community medicine

Published: November 07, 2014

Showing 1-12 of 14

Last Updated: 09/26/2026