Výsledky vyhledávání - Osama H. Ababneh

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  1. 1
    Enucleation and evisceration at a tertiary care hospital in a developing country

    Enucleation and evisceration at a tertiary care hospital in a developing country Autor Osama H. Ababneh, Eman A. AboTaleb, Mohammad A. Abu Ameerh, Yacoub A. Yousef

    Vydáno 2015
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  2. 2
    Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling

    Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling Autor Jing Tian, Ling Ling, Mohammad Shboul, Hane Lee, Brian D. O’Connor, Barry Merriman, Stanley F. Nelson, Simon M. Cool, Osama H. Ababneh, Azmy M. Al-Hadidy, Amira Masri, Hanan Hamamy, Bruno Reversade

    Vydáno 2010
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  3. 3
    Mesenchymal stem cells and conditioned media in the treatment of multiple sclerosis patients: Clinical, ophthalmological and radiological assessments of safety and efficacy

    Mesenchymal stem cells and conditioned media in the treatment of multiple sclerosis patients: Clinical, ophthalmological and radiological assessments of safety and efficacy Autor Said Dahbour, Fatima Jamali, Dana Alhattab, Ali Al‐Radaideh, Osama H. Ababneh, Nosaiba Tawfik Al-Ryalat, Muawyeh Al‐Bdour, Bayan Hourani, Mohammed Msallam, Murad Rasheed, Ammar Huneiti, Yacoub Bahou, Emad S. Tarawneh, Abdalla Awidi

    Vydáno 2017
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  4. 4
    Delayed Intravitreal Anti-VEGF Therapy for Patients During the COVID-19 Lockdown: An Ethical Endeavor

    Delayed Intravitreal Anti-VEGF Therapy for Patients During the COVID-19 Lockdown: An Ethical Endeavor Autor Mutasem Elfalah, Saif Aldeen AlRyalat, Mario Damiano Toro, Robert Ręjdak, Sandrine Zweifel, Rashed Mustafa Nazzal, Mohammed Abu‐Ameerh, Osama H. Ababneh, Almutez Gharaibeh, Zuhair Sharif, Jehad Meqbil, Mo’ath AlShawabkeh, Amal Alwreikat, Muawyah Al Bdour, Maysa Al‐Hussaini, Yacoub A. Yousef

    Vydáno 2021
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  5. 5
    INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex

    INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex Autor Lauren G. Mascibroda, Mohammad Shboul, Nathan D. Elrod, Laurence Colleaux, Hanan Hamamy, Kai-Lieh Huang, Natoya Peart, Moirangthem Kiran Singh, Hane Lee, Barry Merriman, Jeanne N. Jodoin, Poojitha Sitaram, Laura A. Lee, Raja Fathalla, Baeth Al‐Rawashdeh, Osama H. Ababneh, Mohammad El-Khateeb, Nathalie Escande‐Beillard, Stanley F. Nelson, Yixuan Wu, Liang Tong, Linda J. Kenney, Sudipto Roy, William K. Russell, Jeanne Amiel, Bruno Reversade, Eric J. Wagner

    Vydáno 2022
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