Search Results - Alsahafi, Ashraf F

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  1. 1
    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children

    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children by Hasosah, Mohammed Y, Iskandarani, Alaa I, Shawli, Ayman I, Alsahafi, Ashraf F, Sukkar, Ghassan A, Qurashi, Mansour A

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  2. 2
    IgG4-related sclerosing mesenteritis in a 7-year-old Saudi girl

    IgG4-related sclerosing mesenteritis in a 7-year-old Saudi girl by Hasosah, Mohammed Y, Satti, Mohamed B, Yousef, Yasmin A, Alzahrani, Daifullah M, Almutairi, Sajdi A, Alsahafi, Ashraf F, Sukkar, Ghassan A, Alzaben, Abdullah A

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  3. 3
    Eosinophilic esophagitis in Saudi children: symptoms, histology and endoscopy results

    Eosinophilic esophagitis in Saudi children: symptoms, histology and endoscopy results by Hasosah, Mohammed Y, Sukkar, Ghassan A, Alsahafi, Ashraf F, Thabit, Adel O, Fakeeh, Mohammed E, Al-Zahrani, Daifulah M, Satti, Mohamed B

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  4. 4
    Perinatal cytomegalovirus hepatitis in Saudi infants: a case series

    Perinatal cytomegalovirus hepatitis in Saudi infants: a case series by Hasosah, Mohammed Y, Kutbi, Suzane Y, Al-Amri, Abdulfattah W, Alsahafi, Ashraf F, Sukkar, Ghassan A, Alghamdi, Khaled J, Jacobson, Kevan

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  5. 5
    Seroconversion of hepatitis B envelope antigen (HBeAg) by entecavir in a child with chronic hepatitis B

    Seroconversion of hepatitis B envelope antigen (HBeAg) by entecavir in a child with chronic hepatitis B by Hasosah, Mohammed Y, Ghandourah, Heba S, Alsahafi, Ashraf F, Sukkar, Ghassan A, Jacobson, Kevan

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  6. 6
    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children

    Neuroblastoma amplified sequence gene mutation: A rare cause of recurrent liver failure in children by Hasosah, Mohammed Y, Iskandarani, Alaa I, Shawli, Ayman I, Alsahafi, Ashraf F, Sukkar, Ghassan A, Qurashi, Mansour A

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