Houda Benrahma

Casablanca, Morocco

Last Updated: 09/26/2026

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Found 35 publications

Celiac Disease Spectrum Among Patients With Iron Deficiency Anemia: A Retrospective Study From a Tertiary Care Center in Morocco.

Celiac Disease Spectrum Among Patients With Iron Deficiency Anemia: A Retrospective Study From a Tertiary Care Center in Morocco.

Journal: Cureus
Published: August 03, 2026

Intravenous Ferric Carboxymaltose Versus Oral Ferrous Sulfate for Iron Deficiency Anemia: A Retrospective Cohort Study of Iron Store Repletion and Safety.

Intravenous Ferric Carboxymaltose Versus Oral Ferrous Sulfate for Iron Deficiency Anemia: A Retrospective Cohort Study of Iron Store Repletion and Safety.

Journal: Cureus
Published: July 04, 2026

Nutritional Impact of High-Dose Melphalan in Autologous Stem Cell Transplantation.

Nutritional Impact of High-Dose Melphalan in Autologous Stem Cell Transplantation.

Journal: Cureus
Published: March 22, 2026

Nutritional Management in Patients With Hematological Malignancies: An Underestimated Supportive Care Issue.

Nutritional Management in Patients With Hematological Malignancies: An Underestimated Supportive Care Issue.

Journal: Cureus
Published: March 04, 2026

Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families.

Mutational spectrum of SLC26A4 and SLC26A5 associated with hereditary hearing loss in Moroccan families.

Journal: Human genomics
Published: January 10, 2026

Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2.

Expanding the genetic spectrum of neurogenetic disorders in moroccan families by exome sequencing: identification of candidate variants in RYR3, POLR3A, and LAMA2.

Journal: Molecular biology reports
Published: December 16, 2025

Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome.

Computational study of deleterious missense SNPs in the USH1G gene implicated in Usher syndrome.

Journal: Journal of biomolecular structure & dynamics
Published: September 02, 2025

Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families.

Novel splice variants implicated in inherited retinal dystrophies in two Moroccan families.

Journal: Molecular biology reports
Published: June 15, 2025

Evaluation of In vitro Vitamin D Supplementation and its Impact on Sperm Quality: A Controlled Experimental Study.

Evaluation of In vitro Vitamin D Supplementation and its Impact on Sperm Quality: A Controlled Experimental Study.

Journal: Journal of human reproductive sciences
Published: May 28, 2025

Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndrome.

Computational study of the potential impact of WHRN protein missense SNPs on WHRN-MYO15A protein complex interaction and their association with Usher syndrome.

Journal: Journal of biomolecular structure & dynamics
Published: May 19, 2025

Genetic diversity of Usher syndrome in Moroccan patients.

Genetic diversity of Usher syndrome in Moroccan patients.

Journal: Human genetics
Published: November 20, 2024

Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.

Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan families.

Journal: Molecular biology reports
Published: April 25, 2024
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Last Updated: 09/26/2026