Search Results - Almajhad, Nabil A

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  1. 1
    Neuronal ceroid lipofuscinoses type 8: Expanding genotype/phenotype diversity-first report from Saudi Arabia

    Neuronal ceroid lipofuscinoses type 8: Expanding genotype/phenotype diversity-first report from Saudi Arabia by Alkhars, Fatimah Z, Bo Ali, Ahmed Y, Almohanna, Mostafa A, Almajhad, Nabil A

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  2. 2
    Neurological expression of an inherited translocation of chromosomal 1 and 7

    Neurological expression of an inherited translocation of chromosomal 1 and 7 by AlMajhad, Nabil A, AlHashem, Amal M, Bouhjar, Inesse A, Tabarki, Brahim M

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  3. 3
    Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures

    Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures by Tabarki, Brahim, AlMajhad, Nabil, AlHashem, Amal, Shaheen, Ranad, Alkuraya, Fowzan S.

    Published in Human genetics
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  4. 4
    Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association?

    Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association? by Alkhars, Fatimah Z, Almajhad, Nabil, Al-Obaid, Jaafer, Alghadeer, Fatimah, Bo Ali, Ahmed Y

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  5. 5
    Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association?

    Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association? by Alkhars, Fatimah Z, Almajhad, Nabil, Al-Obaid, Jaafer, Alghadeer, Fatimah, Bo Ali, Ahmed Y

    Published in Cureus
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