Search Results - "Alfaraidi, Huda"

Healthcare workers experience in dealing with Coronavirus (COVID-19) pandemic by Almaghrabi, Rana H, Alfaraidi, Huda A, Al Hebshi, Wejdan A, Albaadani, Mohammed M

“…To analyze healthcare workers experiences in dealing with the Coronavirus (COVID-19) pandemic. Methods: An anonymous open web-based survey study was conducted…”
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Wolman's disease presenting with secondary hemophagocytic lymphohistiocytosis: a case report from Saudi Arabia and literature review by Alabbas, Fahad, Elyamany, Ghaleb, Alanzi, Talal, Ali, Tahani Bin, Albatniji, Fatma, Alfaraidi, Huda

“…Hemophagocytic lymphohistiocytosis (HLH) is a rare and potentially fatal syndrome that is characterized by strong activation of the immune system from…”
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Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation by Altawil, Lama, Alshihry, Hind, Alfaraidi, Huda, Alhashem, Amal, Alhumidi, Ahmed, Alkuraya, Fowzan S.

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Genotype and Phenotype of Adenosine Deaminase 2 Deficiency: a Report from Saudi Arabia by Alabbas, Fahad, Alanzi, Talal, Alrasheed, Abdulrahman, Essa, Mohammed, Elyamany, Ghaleb, Asiri, Abdulrahman, Almutairi, Sajdi, Al-Mayouf, Sulaiman, Alenazi, Abdullatif, Alsafadi, Danyah, Ballourah, Walid, Albalawi, Naif, Hanafy, Ehab, Al-Hebshi, Abdulqader, Alrashidi, Seham, Albatniji, Fatma, Alfaraidi, Huda, Ali, Tahani Bin, Al Qwaiee, Mansour, AlHilali, Maryam, Aldeeb, Hayam, Alhaidey, Ali, Aljasem, Hassan, Althubaiti, Sami, Alsultan, Abdulrahman

“…Adenosine deaminase 2 deficiency (DADA2), a rare and potentially fatal systemic autoinflammatory disease, is characterized by low or lack of ADA2 activity due…”
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Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation by Altawil, Lama, Alshihry, Hind, Alfaraidi, Huda, Alhashem, Amal, Alhumidi, Ahmed, Alkuraya, Fowzan S

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