Neziha Khouja-Gouider

15, Rue Djebel Lakhdhar
La Rabta, 1007, Tunisia

Last Updated: 09/26/2026

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Found 19 publications

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

Association of Amyotrophic Lateral Sclerosis and Dopa-responsive dystonia in a Tunisian patient.

Association of Amyotrophic Lateral Sclerosis and Dopa-responsive dystonia in a Tunisian patient.

Journal: Parkinsonism & related disorders

Published: July 31, 2024

Collecting Feedback From Neurologists and Patients to Guide Development of a Parkinson Disease App (DigiPark): Qualitative, Noninterventional Study.

Collecting Feedback From Neurologists and Patients to Guide Development of a Parkinson Disease App (DigiPark): Qualitative, Noninterventional Study.

Journal: JMIR human factors

Published: November 30, 2023

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.

Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review.

Journal: Molecular cytogenetics

Published: August 01, 2022

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.

Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.

Journal: Neuropediatrics

Published: June 30, 2021

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation.

First report of an unusual novel double mutation affecting the transcription repression domain of MeCP2 and causing a severe phenotype of Rett syndrome: Molecular analyses and computational investigation.

Journal: Biochemical and biophysical research communications

Published: January 27, 2018

Status dystonicus in childhood.

Status dystonicus in childhood.

Journal: La Tunisie medicale

Published: June 02, 2016

Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration.

Elevated aspartate aminotransferase and lactate dehydrogenase levels are a constant finding in PLA2G6-associated neurodegeneration.

Journal: European journal of neurology

Published: August 10, 2015

Post-herpes simplex encephalitis chorea: Viral replication or immunological mechanism?

Post-herpes simplex encephalitis chorea: Viral replication or immunological mechanism?

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: July 03, 2014

Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.

Infantile and childhood onset PLA2G6-associated neurodegeneration in a large North African cohort.

Journal: European journal of neurology

Published: January 17, 2014

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.

Journal: Orphanet journal of rare diseases

Published: January 14, 2014

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.

Journal: Brain & development

Published: January 13, 2014

Showing 1-12 of 19

Last Updated: 09/26/2026