Roeya Kolsi

Sfax, 3029, Tunisia

Last Updated: 09/26/2026

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Found 10 publications

Expanding the Clinical Spectrum of SCN8A-Related Epileptic Encephalopathy: Additional Auditory Impairment, Atypical MRI Abnormalities and Putative Mitochondrial Involvement.

Expanding the Clinical Spectrum of SCN8A-Related Epileptic Encephalopathy: Additional Auditory Impairment, Atypical MRI Abnormalities and Putative Mitochondrial Involvement.

Journal: Journal of molecular neuroscience : MN

Published: October 09, 2025

Pediatric Endobronchial Carcinoid Tumors: Report of Two Cases.

Pediatric Endobronchial Carcinoid Tumors: Report of Two Cases.

Journal: Indian journal of pediatrics

Published: April 25, 2025

EBV-associated leiomyosarcoma in an immunocompromised child: A unique intracranial case with genomic study.

EBV-associated leiomyosarcoma in an immunocompromised child: A unique intracranial case with genomic study.

Journal: International journal of surgery case reports

Published: January 13, 2025

Progressive familial intrahepatic cholestasis type 5 due to a novel mutation in the NR1H4 gene.

Progressive familial intrahepatic cholestasis type 5 due to a novel mutation in the NR1H4 gene.

Journal: BMC pediatrics

Published: January 09, 2025

Study of clinical manifestations and etiologies of megaloblastic anemia in children.

Study of clinical manifestations and etiologies of megaloblastic anemia in children.

Journal: Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine

Published: August 05, 2024

Chronic immune thrombocytopenic purpura in children: Clinical presentations and management.

Chronic immune thrombocytopenic purpura in children: Clinical presentations and management.

Journal: La Tunisie medicale

Published: May 30, 2024

A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.

A novel homozygous PIGO mutation associated with severe infantile epileptic encephalopathy, profound developmental delay and psychomotor retardation: structural and 3D modelling investigations and genotype-phenotype correlation.

Journal: Metabolic brain disease

Published: May 09, 2023

Rheumatic cardiopathies and its risk factors: about 50 cases

Rheumatic cardiopathies and its risk factors: about 50 cases

Journal: Annales de cardiologie et d'angeiologie

Published: April 17, 2023

Miliary tuberculosis mimicking COVID-19 multisystemic inflammatory syndrome in children.

Miliary tuberculosis mimicking COVID-19 multisystemic inflammatory syndrome in children.

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

Published: December 03, 2022

Fulminant mulch pneumonitis in a previously healthy child.

Fulminant mulch pneumonitis in a previously healthy child.

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

Published: April 23, 2018

Showing 1-10 of 10

Last Updated: 09/26/2026