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I Ben Youssef-Turki

Showing results (1-10 of 7) with videos related to

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Revue Neurologique|October 10, 2006
[Type I glutaric aciduria: an unrecognized cause of progressive dystonia]N Gouider-Khouja, I Ben Youssef-Turki
Revue Neurologique|June 24, 2014
[Botulinum toxin in the management of spasticity in children]H Benrhouma, J Yacoubi, I Kraoua, et al.
Revue Neurologique|January 27, 2009
[An overview of neurometabolic diseases in Tunisia. a 3-year prospective study]I Kraoua, H Benrhouma, A Rouissi, et al.
Revue Neurologique|November 18, 2015
[Acute disseminated encephalomyelitis in Tunisia: Report of a pediatric cohort]N Ben Achour, O Ben Waddey, I Kraoua, et al.
Neuro-Chirurgie|April 20, 2013
[Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension]N Ben Achour, I Kraoua, A Rouissi, et al.
Molecular Genetics & Genomic Medicine|November 2, 2020
SQSTM1 mutation: Description of the first Tunisian case and literature reviewM Akkari, I Kraoua, H Klaa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 30, 2017
Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian childT Ben Younes, I Kraoua, H Benrhouma, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Revue Neurologique|October 10, 2006
[Type I glutaric aciduria: an unrecognized cause of progressive dystonia]N Gouider-Khouja, I Ben Youssef-Turki
Revue Neurologique|June 24, 2014
[Botulinum toxin in the management of spasticity in children]H Benrhouma, J Yacoubi, I Kraoua, et al.
Revue Neurologique|January 27, 2009
[An overview of neurometabolic diseases in Tunisia. a 3-year prospective study]I Kraoua, H Benrhouma, A Rouissi, et al.
Revue Neurologique|November 18, 2015
[Acute disseminated encephalomyelitis in Tunisia: Report of a pediatric cohort]N Ben Achour, O Ben Waddey, I Kraoua, et al.
Neuro-Chirurgie|April 20, 2013
[Congenital stenosis of interventricular foramina revealed by recurrent intracranial hypertension]N Ben Achour, I Kraoua, A Rouissi, et al.
Molecular Genetics & Genomic Medicine|November 2, 2020
SQSTM1 mutation: Description of the first Tunisian case and literature reviewM Akkari, I Kraoua, H Klaa, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 30, 2017
Pyridoxine-dependent epilepsy: A novel mutation in a Tunisian childT Ben Younes, I Kraoua, H Benrhouma, et al.
Pageof 1