Aida Rouissi
Tunis, Tunisia
Last Updated: 09/26/2026
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Found 24 publications
Expanding the Phenotypic Spectrum of Trafficking Protein Particle Complex Subunit 9-Related Intellectual Developmental Disorder: Prader-Willi-like Presentation in a Tunisian Family.
Journal: Genetic testing and molecular biomarkers
Published: July 08, 2026
Subacute Sclerosing Panencephalitis in a North African Cohort: Findings From the Post-Measles Epidemic Era.
Journal: Sage open pediatrics
Published: January 08, 2025
Genetic investigation of the ubiquitin-protein ligase E3A gene as putative target in Angelman syndrome.
Journal: World journal of clinical cases
Published: October 31, 2023
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
Acute Movement Disorders in Childhood: A Cohort Study and Review of the Literature.
Journal: Pediatric emergency care
Published: September 01, 2021
Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort.
Journal: Journal of immunology research
Published: November 21, 2020
SQSTM1 mutation: Description of the first Tunisian case and literature review.
Journal: Molecular genetics & genomic medicine
Published: July 29, 2020
Rasmussen's Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review.
Journal: Case reports in neurological medicine
Published: March 07, 2020
Muscle-Specific Kinase Autoimmune Myasthenia Gravis: Report of a Pediatric Case and Literature Review.
Journal: Neuropediatrics
Published: December 22, 2018
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
Last Updated: 09/26/2026