Search Results - Rahbeeni, Ahmad A

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  1. 1
    From Symptoms to Diagnosis: An Observational Study of the Journey of SLE Patients in Saudi Arabia

    From Symptoms to Diagnosis: An Observational Study of the Journey of SLE Patients in Saudi Arabia by Karremah, Mishal F, Hassan, Rola Y, Faloudah, Ammar Z, Alharbi, Lujain K, Shodari, Albraa F, Rahbeeni, Ahmad A, Alharazi, Nouf K, Binjabi, Ahmad Z, Cheikh, Mohamed M, Manasfi, Hanadi, Abdulaziz, Sultana, Hussein, Albadr Hamza, Alhazmi, Ahmed, Almoallim, Hani

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  2. 2
    Phenotypic expansion of Zimmermann- Laband syndrome associated with cardiac and hearing loss: a case report

    Phenotypic expansion of Zimmermann- Laband syndrome associated with cardiac and hearing loss: a case report by Galal, Mohammed, Mashali, Mohamed, Zaheer, Ahmad, Rahbeeni, Zuhair

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  3. 3
    In search of triallelism in Bardet-Biedl syndrome

    In search of triallelism in Bardet-Biedl syndrome by ABU-SAFIEH, Leen, AL-ANAZI, Shamsa, AL-SALEM, Ahmad, ALRASHED, May, FAQEIH, Eissa, SOFTAH, Ameen, AL-HASHEM, Amal, WALI, Sami, RAHBEENI, Zuhair, ALSAYED, Moeen, KHAN, Arif O, AL-GAZALI, Lihadh, AL-ABDI, Lama, TASCHNER, Peter Em, AL-HAZZAA, Selwa, ALKURAYA, Fowzan S, HASHEM, Mais, ALKURAYA, Hisham, ALAMR, Mushari, SIRELKHATIM, Mugtaba O, AL-HASSNAN, Zuhair, ALKURAYA, Basim, MOHAMED, Jawahir Y

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  4. 4
    Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome

    Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome by Altassan, Ruqaiah, Qudair, Ahmad, Alokaili, Riyadh, Alhasan, Khalid, Faqeih, Eissa A., Alhashem, Amal, Alowain, Muhammed, Alsayed, Moeanaldeen, Rahbeeni, Zuhair, Albadi, Lama, Alkuraya, Fowzan S., Anderson, Eric N., Rajan, Deepa, Pandey, Udai Bhan

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  5. 5
    Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

    Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency by Faiyaz-Ul-Haque, Muhammad, Al-Owain, Mohammed, Al-Dayel, Fouad, Al-Hassnan, Zuhair, Al-Zaidan, Hamad, Rahbeeni, Zuhair, Al-Sayed, Moeen, Balobaid, Ameera, Cluntun, Ahmad, Toulimat, Mohamed, Abalkhail, Hala, Peltekova, Iskra, Zaidi, Syed H. E.

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  6. 6
    Novel FBPI gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency

    Novel FBPI gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency by FAIYAZ-UL-HAQUE, Muhammad, AL-OWAIN, Mohammed, ABALKHAIL, Hala, PELTEKOVA, Iskra, ZAIDI, Syed H. E, AL-DAYEL, Fouad, AL-HASSNAN, Zuhair, AL-ZAIDAN, Hamad, RAHBEENI, Zuhair, AL-SAYED, Moeen, BALOBAID, Ameera, CLUNTUN, Ahmad, TOULIMAT, Mohamed

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