Hanene Benrhouma

Tunis, Tunisia

Last Updated: 09/26/2026

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Found 40 publications

A transposase-derived gene required for human brain development.

A transposase-derived gene required for human brain development.

Journal: Science advances

Published: January 14, 2026

A founder variant in Tunisian PMM2-CDG patients: An integrated clinical, radiological, biochemical, and genetic study.

A founder variant in Tunisian PMM2-CDG patients: An integrated clinical, radiological, biochemical, and genetic study.

Journal: Molecular genetics and metabolism

Published: August 06, 2025

Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus Guidelines.

Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus Guidelines.

Journal: Pediatrics

Published: May 13, 2025

A Tunisian POLG mutation expands the clinical spectrum of POLG-related disorders.

A Tunisian POLG mutation expands the clinical spectrum of POLG-related disorders.

Journal: Mitochondrion

Published: April 27, 2025

Subacute Sclerosing Panencephalitis in a North African Cohort: Findings From the Post-Measles Epidemic Era.

Subacute Sclerosing Panencephalitis in a North African Cohort: Findings From the Post-Measles Epidemic Era.

Journal: Sage open pediatrics

Published: January 08, 2025

Post-mumps encephalitis mimicking metabolic disease on brain magnetic resonance imaging: a case report.

Post-mumps encephalitis mimicking metabolic disease on brain magnetic resonance imaging: a case report.

Journal: Pediatric radiology

Published: September 08, 2024

Biotinidase Deficiency: Report of a Tunisian Case With Neuromyelitis Optica-Like Presentation and Review of the Literature.

Biotinidase Deficiency: Report of a Tunisian Case With Neuromyelitis Optica-Like Presentation and Review of the Literature.

Journal: Case reports in neurological medicine

Published: March 20, 2024

Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families.

Tremor Ataxia With Central Hypomyelation Phenotype Related to a Recurrent POLR3A Mutation in Six Unrelated Tunisian Families.

Journal: Molecular genetics & genomic medicine

Published: February 28, 2024

RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.

RTN2 deficiency results in an autosomal recessive distal motor neuropathy with lower limb spasticity.

Journal: Brain : a journal of neurology

Published: August 30, 2023

A transposase-derived gene required for human brain development.

A transposase-derived gene required for human brain development.

Journal: bioRxiv : the preprint server for biology

Published: May 10, 2023

Pediatric Neurotuberculosis: A cases series and review of the literature.

Pediatric Neurotuberculosis: A cases series and review of the literature.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: May 31, 2022

Manic syndrome in mitochondrial membrane protein-associated neurodegeneration: A case report.

Manic syndrome in mitochondrial membrane protein-associated neurodegeneration: A case report.

Journal: Psychiatry and clinical neurosciences

Published: April 05, 2022

Showing 1-12 of 40

Last Updated: 09/26/2026