Search Results - Issa, M.Y.

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  1. 1
    Hypermanganesemia with dystonia, polycythemia and cirrhosis in 10 patients: Six novel SLC30A10 mutations and further phenotype delineation

    Hypermanganesemia with dystonia, polycythemia and cirrhosis in 10 patients: Six novel SLC30A10 mutations and further phenotype delineation by Zaki, M.S., Issa, M.Y., Elbendary, H.M., El‐Karaksy, H., Hosny, H., Ghobrial, C., El Safty, A., El‐Hennawy, A., Oraby, A., Selim, L., Abdel‐Hamid, M.S.

    Published in Clinical genetics
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  2. 2
    PGAP3‐related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation

    PGAP3‐related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation by Abdel‐Hamid, M.S., Issa, M.Y., Otaify, G.A., Abdel‐Ghafar, S.F., Elbendary, H.M., Zaki, M.S.

    Published in Clinical genetics
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  3. 3
    Optimization of fuel briquette made from bi-composite biomass for domestic heating applications

    Optimization of fuel briquette made from bi-composite biomass for domestic heating applications by Oladosu, K.O., Babalola, S.A., Kareem, M.W., Ajimotokan, H.A., Kolawole, M.Y., Issa, W.A., Olawore, A.S., Ponle, E.A.

    Published in Scientific African
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  4. 4
    Electrical properties of charge transfer complexes of diaminonaphthalene donors with dinitro- and trinitrobenzene acceptors

    Electrical properties of charge transfer complexes of diaminonaphthalene donors with dinitro- and trinitrobenzene acceptors by Ayad, Mohamad M.Y., Amer, Saiid A., Issa, Raafat M.

    Published in Thermochimica acta
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