Search Results - Samadi, Abdelmohsin

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  1. 1
    GABA transaminase deficiency. Case report and literature review

    GABA transaminase deficiency. Case report and literature review by Oshi, Amira, Alfaifi, Abdullah, Seidahmed, Mohammed Z., Al Hussein, Khalid, Miqdad, Abeer, Samadi, Abdelmohsin, Abdelbasit, Omar

    Published in Clinical case reports
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  2. 2
    Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy

    Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy by Seidahmed, Mohammed Zain, Salih, Mustafa A., Abdelbasit, Omer Bashir, Alassiri, Ali H., Hussein, Khalid Al, Miqdad, Abeer, Samadi, Abdelmohsin, Rasheed, Abdallah Al, Alorainy, Ibrahim A., Shaheen, Ranad, Alkuraya, Fowzan S.

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    Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy

    Gonadal mosaicism for ACTA1 gene masquerading as autosomal recessive nemaline myopathy by Seidahmed, Mohammed Zain, Salih, Mustafa A, Abdelbasit, Omer Bashir, Alassiri, Ali H, Hussein, Khalid Al, Miqdad, Abeer, Samadi, Abdelmohsin, Rasheed, Abdallah Al, Alorainy, Ibrahim A, Shaheen, Ranad, Alkuraya, Fowzan S

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