Hind Dehbi

Casablanca, Morocco

Last Updated: 09/26/2026

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Found 44 publications

Molecular profiling of coronary stent restenosis. A systematic review and functional analysis of implicated genes: Erratum.

Molecular profiling of coronary stent restenosis. A systematic review and functional analysis of implicated genes: Erratum.

Journal: Medicine
Published: July 25, 2026

Epidemiological and Biological Profiles of Constitutional Coagulation Deficiencies at CHU Ibn Rochd Hematology Laboratory.

Epidemiological and Biological Profiles of Constitutional Coagulation Deficiencies at CHU Ibn Rochd Hematology Laboratory.

Journal: Clinical laboratory
Published: July 07, 2026

Minimal Residual Disease of T Acute Lymphoblastic Leukemia: the Experience of University Hospital Center Casablanca - Morocco.

Minimal Residual Disease of T Acute Lymphoblastic Leukemia: the Experience of University Hospital Center Casablanca - Morocco.

Journal: Clinical laboratory
Published: October 13, 2025

Molecular Aspects of Rare Coagulation Factor Deficiencies.

Molecular Aspects of Rare Coagulation Factor Deficiencies.

Journal: Cureus
Published: July 30, 2025

Genetic Variations in TLR2 and TLR4 Genes and Their Association With COVID-19 Severity and Inflammatory Markers in the Moroccan Population.

Genetic Variations in TLR2 and TLR4 Genes and Their Association With COVID-19 Severity and Inflammatory Markers in the Moroccan Population.

Journal: International journal of immunogenetics
Published: June 08, 2025

Molecular profiling of coronary stent testenosis: A systematic review and functional analysis of implicated genes.

Molecular profiling of coronary stent testenosis: A systematic review and functional analysis of implicated genes.

Journal: Medicine
Published: June 02, 2025

The Interleukin-6 gene variants may protect against SARS-CoV-2 infection and the severity of COVID-19: a case-control study in a Moroccan population.

The Interleukin-6 gene variants may protect against SARS-CoV-2 infection and the severity of COVID-19: a case-control study in a Moroccan population.

Journal: BMC medical genomics
Published: January 23, 2024

t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report.

t(1;4) translocation in a child with acute lymphoblastic leukemia: a case report.

Journal: Journal of medical case reports
Published: September 05, 2023

A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report.

A novel SCN8A variant of unknown significance in pediatric epilepsy: a case report.

Journal: The Journal of international medical research
Published: July 27, 2023

The peroxisome proliferator-activated receptor γ coactivator-1 alpha rs8192678 (Gly482Ser) variant and hepatitis B virus clearance.

The peroxisome proliferator-activated receptor γ coactivator-1 alpha rs8192678 (Gly482Ser) variant and hepatitis B virus clearance.

Journal: Infectious diseases (London, England)
Published: June 28, 2023

Prognostic value of residual disease detection in acute myeloid leukemia with normal karyotype and negative FLT3-ITD

Prognostic value of residual disease detection in acute myeloid leukemia with normal karyotype and negative FLT3-ITD

Journal: Annales de biologie clinique
Published: May 05, 2023

Novel FREM1 homozygous variant in an individual with an intermediate phenotype between Bifid Nose with or without Anorectal and Renal Anomalies and Manitoba-oculo-tricho-anal syndromes.

Novel FREM1 homozygous variant in an individual with an intermediate phenotype between Bifid Nose with or without Anorectal and Renal Anomalies and Manitoba-oculo-tricho-anal syndromes.

Journal: Clinical dysmorphology
Published: December 12, 2022
Showing 1-12 of 44

Last Updated: 09/26/2026