EMNA BARKAOUI

Employment

• Children Hospital, Tunis Pediatrician MD PhD, Head of Department
  2007 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (8)

• Novel mutations in Uridyl-diphosphate-glucuronosyl-transferase 1A1 (UGT1A1) gene in Tunisian patients with unconjugated hyperbilirubinemia.
  European journal of medical genetics 2021 DOI: 10.1016/j.ejmg.2021.104139
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• Cholestasis with Normal Gammaglutamyl Transferasis from Management to Molecular Investigation with Novel Mutations in ATP8B1 and ABCB11: Tunisian Study
  Journal of Genetic Disorders 2018
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• Niemann-Pick disease type C in patients enzymatically proven and novel mutations defined the first report from Libya and review of literature
  Biochemistry & Molecular Biology Journal 2018 DOI: 10.21767/2471-8084-c3-015
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• Experience of a Single Center in NTBC Use in Management of Hereditary Tyrosinemia Type I in Libya.
  Iranian journal of pediatrics 2015 DOI: 10.5812/ijp.3608
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• Clinical Variability among Patients with Gilbert Syndrome
  Journal of Molecular Biomarkers & Diagnosis 2014 DOI: 10.4172/2155-9929.1000201
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• Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
  Journal of inherited metabolic disease 2007 DOI: 10.1007/s10545-007-0737-1
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• [Favorable outcome of treatment with NTBC of acute liver insufficiency disclosing hereditary tyrosinemia type I].
  Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 1999 DOI: 10.1016/s0929-693x(99)80562-4
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• [Leigh syndrome and leukodystrophy due to partial succinate dehydrogenase deficiency: regression with riboflavin].
  Archives de pediatrie : organe officiel de la Societe francaise de pediatrie 1999 DOI: 10.1016/s0929-693x(99)80224-3
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