Search Results - Ghizlane, Zouiri

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  1. 1
    Diagnostic accuracy of the lactate stress test for detecting mitochondrial disorders: Systematic review and meta-analysis

    Diagnostic accuracy of the lactate stress test for detecting mitochondrial disorders: Systematic review and meta-analysis by El Guessabi, Sara, Abouqal, Redouane, Ibrahimi, Azeddine, Zouiri, Ghizlane, Sfifou, Fatima, Finsterer, Josef, Kriouile, Yamna

    Published in Heliyon
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  2. 2
    c.754T>A homozygous mutation described for the first time in three Moroccan patients with Gaucher disease

    c.754T>A homozygous mutation described for the first time in three Moroccan patients with Gaucher disease by Zouiri, Ghizlane, Rhouda, Hajar, Kriouile, Yamna

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  3. 3
    Pathologic Confirmation of Lafora Disease

    Pathologic Confirmation of Lafora Disease by Rhouda, Hajar, Malihy, Abderrahmane, Zouiri, Ghizlane, Kriouile, Yamna

    Published in Pediatric neurology
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  4. 4
    Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder

    Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder by Rochdi, Khaoula, Cerino, Mathieu, Da Silva, Nathalie, Delague, Valerie, Bouzidi, Aymane, Nahili, Halima, Zouiri, Ghizlane, Kriouile, Yamna, Gorokhova, Svetlana, Bartoli, Marc, Saïle, Rachid, Barakat, Abdelhamid, Krahn, Martin

    Published in Clinica chimica acta
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  5. 5
    A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration

    A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration by Efthymiou, Stephanie, Kriouile, Yamna, Salpietro, Vincenzo, Hajar, Rhouda, Ghizlane, Zouiri, Mankad, Kshitij, El Khorassani, Mohamed, Aguennouz, Mhammed, Houlden, Henry, Wiethoff, Sarah

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  6. 6
    Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder

    Clinical and genetic characterization of a progressive RBL2-associated neurodevelopmental disorder by Aughey, Gabriel N, Cali, Elisa, Maroofian, Reza, Zaki, Maha S, Pagnamenta, Alistair T, Ali, Zafar, Abdulllah, Uzma, Rahman, Fatima, Menzies, Lara, Shafique, Anum, Suri, Mohnish, Roze, Emmanuel, Aguennouz, Mohammed, Ghizlane, Zouiri, Saadi, Saadia Maryam, Fatima, Ambrin, Cheema, Huma Arshad, Anjum, Muhammad Nadeem, Morel, Godelieve, Robin, Stephanie, McFarland, Robert, Altunoglu, Umut, Kraus, Verena, Shoukier, Moneef, Murphy, David, Flemming, Kristina, Yttervik, Hilde, Rhouda, Hajar, Lesca, Gaetan, Chatron, Nicolas, Rossi, Massimiliano, Murtaza, Bibi Nazia, Ur Rehman, Mujaddad, Lord, Jenny, Giacopuzzi, Edoardo, Hayat, Azam, Siraj, Muhammad, Badv, Reza Shervin, Seo, Go Hun, Beetz, Christian, Kayserili, Hülya, Krioulie, Yamna, Chung, Wendy K, Naz, Sadaf, Maqbool, Shazia, Chandler, Kate, Kershaw, Christopher, Wright, Thomas, Banka, Siddharth, Gleeson, Joseph G, Taylor, Jenny C, Efthymiou, Stephanie, Baig, Shahid Mahmood, Severino, Mariasavina, Jepson, James E C, Houlden, Henry

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  7. 7
    GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families

    GNE Myopathy and Duchenne Muscular Dystrophy in Two Moroccans Families by Sifeddine, N., Amalou, G., Charif, M., Nahili, H., Bouzidi, A., Salaheddine, R., Morjane, I., Zouiri, G., Kriouile, Y., Elkhalfi, B., Lenaers, G., Barakat, A.

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  8. 8
    A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration

    A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration by Efthymiou, Stephanie, Kriouile, Yamna, Salpietro, Vincenzo, Hajar, Rhouda, Ghizlane, Zouiri, Mankad, Kshitij, El Khorassani, Mohamed, Aguennouz, Mhammed, Houlden, Henry, Wiethoff, Sarah

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