Search Results - Mohamed, Zakkiriah

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  1. 1
    A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients

    A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients by Musa, Sara, Eyaid, Wafaa, Kamer, Kimberli, Ali, Rehab, Al-Mureikhi, Mariam, Shahbeck, Noora, Al Mesaifri, Fatma, Makhseed, Nawal, Mohamed, Zakkiriah, AlShehhi, Wafaa Ali, Mootha, Vamsi K., Juusola, Jane, Ben-Omran, Tawfeg

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  2. 2
    Parry-Romberg syndrome in Kuwait

    Parry-Romberg syndrome in Kuwait by Zakkiriah Mohamed, Al Khalaf Maryam KH, Al Mutairi Muna A, Sarah, Al Enezi

    Published in Saudi medical journal
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  3. 3
    Parry-Romberg syndrome in Kuwait. Neurological manifestations in 2 children

    Parry-Romberg syndrome in Kuwait. Neurological manifestations in 2 children by Zakkiriah, Mohammed, Al Khalaf, Maryam Kh, Al Mutairi, Muna A, Al Enezi, Sarah

    Published in Saudi medical journal
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  4. 4
    Phacomatosis pigmentovascularis: Report of four new cases

    Phacomatosis pigmentovascularis: Report of four new cases by Nanda, Arti, Al-Abdulrazzaq, Hamad, Habeeb, Yousif, Zakkiriah, Mohamed, Alghadhfan, Faisal, Al-Noun, Rana, Al-Ajmi, Hejab

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