IK
Ichraf Kraoua

Publications (6)

Case Report: Overlap syndrome of anti–NMDA receptor encephalitis and MOG-associated disease in a pediatric patient—literature insights
Article scientifique · 2026
Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Erratum · 2024
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health
Article scientifique · 2024
Heterogeneous clinical features in Cockayne syndrome patients and siblings carrying the same CSA mutations
Article scientifique · 2022
Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment
Article scientifique · 2021
Heterogeneous clinical features in Cockayne syndrome-A patients with the same mutation and in siblings
Article scientifique · 2021

Domaines principaux

Sciences de la santé4 Sciences de la vie et biotechnologies2

Statistiques

Consultations13
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