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EMNA BARKAOUI

Research Profile

Chemicals & Drugs

Disorders

Living Beings

Infants

Activities & Behaviors

Child Language

Geographic Areas

Tunisia

Anatomy

Pyramidal Tracts

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Co-author Network

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Publications

TOP 3
EMNA BARKAOUI; W Cherif; Néji Tebib; Cherine Charfeddine; F Ben Rhouma; H Azzouz; A Ben Chehida; Kamel Monastiri; Jalel Chemli; Fethi Amri; Hadhami Ben Turkia; Mohamed Slim Abdelmoula; Neziha Kaabachi; Sonia Abdelhak; Mohamed Ben Dridi
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
EMNA BARKAOUI; D Debray; D Habès; H Ogier; O Bernard
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I].
Jean-Marc Pinard; Cécile Marsac; EMNA BARKAOUI; Isabelle Desguerre; M Birch-Machin; P Reinert; Gérard Ponsot
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin].

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All Publications

2007: EMNA BARKAOUI; W Cherif; Néji Tebib; Cherine Charfeddine; F Ben Rhouma; H Azzouz; A Ben Chehida; Kamel Monastiri; Jalel Chemli; Fethi Amri; Hadhami Ben Turkia; Mohamed Slim Abdelmoula; Neziha Kaabachi; Sonia Abdelhak; Mohamed Ben Dridi
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
Journal of inherited metabolic disease 2007;30(6):989.
1999: EMNA BARKAOUI; D Debray; D Habès; H Ogier; O Bernard
[Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1999;6(5):540-4.
1999: Jean-Marc Pinard; Cécile Marsac; EMNA BARKAOUI; Isabelle Desguerre; M Birch-Machin; P Reinert; Gérard Ponsot
[Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1999;6(4):421-6.

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