Hasil Pencarian - Ahmed Al-Rumayyan

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  1. 1
    Familial Hemiplegic Migraine with Prolonged Coma and Hyperthermia: ATP1A2 Gene Mutation Case Report in a Single Saudi Family.

    Familial Hemiplegic Migraine with Prolonged Coma and Hyperthermia: ATP1A2 Gene Mutation Case Report in a Single Saudi Family. oleh Waleed Altwaijri, Fuad Almalki, Ahmed Al-Rumayyan, Safiyyah Asiri

    Diterbitkan 2019-06-01
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  2. 2
    Prognostic factors and treatment outcomes in pediatric autoimmune encephalitis: a multicenter study

    Prognostic factors and treatment outcomes in pediatric autoimmune encephalitis: a multicenter study oleh Ahlam Ahmed Abu Melha, Ahlam Ahmed Abu Melha, Ahlam Ahmed Abu Melha, Ahlam Ahmed Abu Melha, Amjad Saad Aldress, Amjad Saad Aldress, Amjad Saad Aldress, Amjad Saad Aldress, Fahad Alamri, Lama Saleh Aljomah, Lama Saleh Aljomah, Lama Saleh Aljomah, Lama Saleh Aljomah, Raid Hommady, Raid Hommady, Raid Hommady, Raid Hommady, Ahmed Al-Rumayyan, Ahmed Al-Rumayyan, Ahmed Al-Rumayyan, Ahmed Al-Rumayyan, Fahad Albassam

    Diterbitkan 2024-09-01
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  3. 3
    Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish

    Mutated VWA8 Is Associated With Developmental Delay, Microcephaly, and Scoliosis and Plays a Novel Role in Early Development and Skeletal Morphogenesis in Zebrafish oleh Muhammad Umair, Muhammad Farooq Khan, Mohammed Aldrees, Marwan Nashabat, Kheloud M. Alhamoudi, Kheloud M. Alhamoudi, Muhammad Bilal, Yusra Alyafee, Abeer Al Tuwaijri, Manar Aldarwish, Ahmed Al-Rumayyan, Hamad Alkhalaf, Mohammad A. M. Wadaan, Majid Alfadhel, Majid Alfadhel

    Diterbitkan 2021-10-01
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  4. 4
    Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening

    Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening oleh Majid Alfadhel, Muhammad Umair, Bader Almuzzaini, Saif Alsaif, Sulaiman A. AlMohaimeed, Maher A. Almashary, Wardah Alharbi, Latifah Alayyar, Abdulrahman Alasiri, Mariam Ballow, Abdulkareem AlAbdulrahman, Monira Alaujan, Marwan Nashabat, Ali Al‐Odaib, Waleed Altwaijri, Ahmed Al‐Rumayyan, Muhammad T. Alrifai, Ahmed Alfares, Mohammed AlBalwi, Brahim Tabarki

    Diterbitkan 2019-10-01
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  5. 5
    The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data

    The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data oleh Majid Alfadhel, Majid Alfadhel, Majid Alfadhel, Mohammed Almuqbil, Mohammed Almuqbil, Fuad Al Mutairi, Fuad Al Mutairi, Muhammad Umair, Mohammed Almannai, Malak Alghamdi, Hamad Althiyab, Rayyan Albarakati, Fahad A. Bashiri, Walaa Alshuaibi, Duaa Ba-Armah, Duaa Ba-Armah, Mohammed A. Saleh, Ali Al-Asmari, Eissa Faqeih, Waleed Altuwaijri, Waleed Altuwaijri, Ahmed Al-Rumayyan, Ahmed Al-Rumayyan, Mohammed Ali Balwi, Mohammed Ali Balwi, Faroug Ababneh, Abdulrahman Faiz Alswaid, Abdulrahman Faiz Alswaid, Wafaa M. Eyaid, Wafaa M. Eyaid, Naif A. M. Almontashiri, Naif A. M. Almontashiri, Amal Alhashem, Amal Alhashem, Khalid Hundallah, Aida Bertoli-Avella, Peter Bauer, Christian Beetz, Muhammad Talal Alrifai, Muhammad Talal Alrifai, Ahmed Alfares, Ahmed Alfares, Brahim Tabarki

    Diterbitkan 2021-05-01
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