Ichraf Kraoua
Tunis University
73 Papers
56 Citations
Ichraf Kraoua is an academic researcher from Tunis University. The author has contributed to research in topics: Medicine & Biology. The author has an hindex of 9, co-authored 41 publications.
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Papers
MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder
Gali Heimer,Juha M. Kerätär,Lisa G. Riley,Shanti Balasubramaniam,Eran Eyal,Laura P. Pietikäinen,J. Kalervo Hiltunen,Dina Marek-Yagel,Jeffrey Hamada,Allison Gregory,Caleb Rogers,Penelope Hogarth,Martha Nance,Nechama Shalva,Alvit Veber,Michal Tzadok,Andreea Nissenkorn,Davide Tonduti,Florence Renaldo,Ichraf Kraoua,Celeste Panteghini,Lorella Valletta,Barbara Garavaglia,Mark J. Cowley,Velimir Gayevskiy,Tony Roscioli,Jonathon M. Silberstein,Chen Hoffmann,Annick Raas-Rothschild,Valeria Tiranti,Yair Anikster,John Christodoulou,Alexander J. Kastaniotis,Bruria Ben-Zeev,Susan J. Hayflick +34 more
TL;DR: The results suggest that mutations in MECR cause a distinct human disorder of the mtFAS pathway, and the observation of decreased lipoylation raises the possibility of a potential therapeutic strategy.
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Movement disorders in neuro-metabolic diseases
TL;DR: The primary goal of this article is to describe the types of movement disorders most frequently observed in NMD and to discuss their clinical value in the setting of specific types of NMD.
35
Movement disorders in neuro-metabolic diseases.
N. Gouider-Khouja,Ichraf Kraoua,Hanene Benrhouma,Narjes Fraj,Aida Rouissi +4 more
TL;DR: The primary goal of this article is to describe the types of movement disorders most frequently observed in NMD and to discuss their clinical value in the setting of specific types of NMD.
20
Novel POLR1C mutation in RNA polymerase III-related leukodystrophy with severe myoclonus and dystonia.
Ichraf Kraoua,Adnane Karkar,Adnane Karkar,Cyrine Drissi,Hanene Benrhouma,Hedia Klaa,Simon Samaan,Florence Renaldo,Monique Elmaleh,Mohamed Ben Hamouda,Sonia Abdelhak,Odile Boespflug-Tanguy,Ilfghem Ben Youssef-Turki,Imen Dorboz +13 more
TL;DR: RNA polymerase III (Pol III)‐related leukodystrophies are a group of autosomal recessive neurodegenerative disorders caused by mutations in PolR3A and POLR3B.
11
Epilepsy Aspects and EEG Patterns in Neuro-Metabolic Diseases
Ilhem Ben Youssef-Turki,Ichraf Kraoua,Sourour Smirani,Kchaou Mariem,Hanene Benrhouma,Aida Rouissi,Neziha Gouider-Khouja +6 more
TL;DR: The seizure type, EEG patterns and response to antiepileptic drugs in NMD and to discuss clinical value of epilepsy type in the setting of specific NMD are described and discussed.