Search Results - Ourteni, I.

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  1. 1
    Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family

    Autosomal recessive congenital cataract, intellectual disability phenotype linked to STX3 in a consanguineous Tunisian family by Chograni, M., Alkuraya, F.S., Ourteni, I., Maazoul, F., Lariani, I., Chaabouni, H.B.

    Published in Clinical genetics
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  2. 2
    Identification of barley landrace genotypes with contrasting salinity tolerance at vegetative growth stage

    Identification of barley landrace genotypes with contrasting salinity tolerance at vegetative growth stage by Chikha, Mariem Ben, Hessini, Kamel, Ourteni, Rim Nefissi, Ghorbel, Abdelwahed, Zoghlami, Nejia

    Published in Plant Biotechnology
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  3. 3
    Two peculiarities of the nutcracker syndrome : rare association with multiples thrombosis and successful medical treatment (Pentoxifylline)

    Two peculiarities of the nutcracker syndrome : rare association with multiples thrombosis and successful medical treatment (Pentoxifylline) by Labidi, Jannet, Ibn Arabiyah, Yusra, Achouch, Sonia, Umrani, Marwah, Ourteni, Imen

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  4. 4
    Two Peculiarities of the Nutcracker Syndrome: Rare Association with Multiples Thrombosis and Successful Medical Treatment (Pentoxifylline)

    Two Peculiarities of the Nutcracker Syndrome: Rare Association with Multiples Thrombosis and Successful Medical Treatment (Pentoxifylline) by Ariba, Yosra Ben, Achouch, Sonia, Omrani, Marwa, Ourteni, Imen, Labidi, Jannet

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  5. 5
    OA71 Le syndrome du canal carpien. Apport de l’echographie

    OA71 Le syndrome du canal carpien. Apport de l’echographie by Alouini-Mekki, R., Allani, M., Alouini, B., Laadhari, H., Bellara, I., Ourteni, M., Nikolova, N.

    Published in Journal de radiologie
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