Houria Abdelghaffar

Mohammedia, 20650, Morocco

Last Updated: 09/26/2026

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Found 12 publications

HLA-DQB1*02, HLA-DRB1*03 alleles and HLA-DQB1*02-HLA-DRB1*03 haplotype confer a significant risk of celiac disease in the Mauritanian population.

HLA-DQB1*02, HLA-DRB1*03 alleles and HLA-DQB1*02-HLA-DRB1*03 haplotype confer a significant risk of celiac disease in the Mauritanian population.

Journal: BMC gastroenterology
Published: March 07, 2026

Concentration and prevalence of mycotoxins in poultry feed and poultry products: a global systematic review and meta-analysis.

Concentration and prevalence of mycotoxins in poultry feed and poultry products: a global systematic review and meta-analysis.

Journal: Mycotoxin research
Published: January 09, 2026

First detection of bovine viral diarrhea virus using antigen capture ELISA and RT-PCR assay in cattle with respiratory and abortive issues in Morocco.

First detection of bovine viral diarrhea virus using antigen capture ELISA and RT-PCR assay in cattle with respiratory and abortive issues in Morocco.

Journal: Journal of advanced veterinary and animal research
Published: September 13, 2025

Insights into Bovine Viral Diarrhea Epidemiology in Moroccan Cattle Population.

Insights into Bovine Viral Diarrhea Epidemiology in Moroccan Cattle Population.

Journal: Veterinaria italiana
Published: September 11, 2024

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

Novel pathogenic WHRN variant causing hearing loss in a moroccan family.

Journal: Molecular biology reports
Published: July 18, 2023

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

Homozygous Missense Variants in FOXI1 and TMPRSS3 Genes Associated with Non-syndromic Deafness in Moroccan Families.

Journal: Biochemical genetics
Published: May 02, 2023

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco.

Journal: Molecular biology reports
Published: August 23, 2021

Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1.

Omenn syndrome caused by a novel homozygous mutation in recombination activating gene 1.

Journal: Immunobiology
Published: July 21, 2020

A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.

A Homozygous RAG1 Gene Mutation in a Case of Combined Immunodeficiency: Clinical, Molecular, and Computational Analysis.

Journal: Human heredity
Published: February 05, 2020

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.

Journal: Journal of immunology research
Published: May 23, 2019

Poikiloderma with Neutropenia in Morocco: a Report of Four Cases.

Poikiloderma with Neutropenia in Morocco: a Report of Four Cases.

Journal: Journal of clinical immunology
Published: November 09, 2016

Association of CD209L tandem repeats polymorphism with susceptibility to human immunodeficiency virus-1 infection, disease progression, and treatment outcomes: a Moroccan cohort study.

Association of CD209L tandem repeats polymorphism with susceptibility to human immunodeficiency virus-1 infection, disease progression, and treatment outcomes: a Moroccan cohort study.

Journal: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
Published: October 06, 2014
Showing 1-12 of 12

Last Updated: 09/26/2026