Showing 1 - 3 results of 3 for search 'Chayma Sahli', query time: 0.02s Refine Results
  1. 1
    Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia

    Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia by Latifa Chkioua, Yessine Amri, Chayma Sahli, Tawfik Nasri, Mohamed Omar Miladi, Taieb Massoud, Sandrine Laradi, Mohamed Ghorbel, Hassen Ben Abdennebi

    Published 2024-11-01
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  2. 2
    Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b

    Identification of mutations that causes glucose-6-phosphate transporter defect in tunisian patients with glycogenosis type 1b by Latifa Chkioua, Yessine Amri, Chayma Sahli, Ferdawes Ben Rhouma, Amel Ben Chehida, Neji Tebib, Taieb Messaoud, Hassen Ben Abdennebi, Sandrine Laradi

    Published 2023-04-01
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  3. 3
    Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa

    Mucopolysaccharidosis type I: founder effect of the p.P533R mutation in North Africa by Latifa Chkioua, Houda El Fissi, Yessine Amri, Chayma Sahli, Fadoua Bouzid, Hela Boudabous, Neji Tbib, Salima Ferchichi, Taieb Massoud, Najat Alif, Sandrine Laradi, Hassen Ben Abdennebi

    Published 2024-10-01
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    Article

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