Hasil Pencarian - Hind Alshihry, MD

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  1. 1
    Integrin α3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction

    Integrin α3 mutation junctional epidermolysis bullosa presenting with hypotrichosis and lacrimal obstruction oleh Hind Alshihry, MD, Shahad D. AlGhamdy, MD, Amal Alhashem, MD, Hind M. Almohanna, MD

    Diterbitkan 2024-01-01
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  2. 2
    Vitamin B12 deficiency secondary to cobalamin F deficiency simulating dyskeratosis congenita

    Vitamin B12 deficiency secondary to cobalamin F deficiency simulating dyskeratosis congenita oleh Lama Altawil, MD, Hind Alshihry, MD, Hala Ahmed, MD, Hanan E. Shamseldin, MD, Fowzan Alkuraya, MD

    Diterbitkan 2020-09-01
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  3. 3
    Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation

    Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutati... oleh Lama Altawil, MD, Hind Alshihry, MD, Huda Alfaraidi, MD, Amal Alhashem, MD, Ahmed Alhumidi, MD, Fowzan S. Alkuraya, MD

    Diterbitkan 2021-08-01
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