Search Results - Naim, Ewa A

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  1. 1
    Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

    Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome by Monies, Dorota M, Al-Hindi, Hindi N, Al-Muhaizea, Mohamed A, Jaroudi, Dyala J, Al-Younes, Banan, Naim, Ewa A, Wakil, Salma M, Meyer, Brian F, Bohlega, Saeed

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  2. 2
    Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis

    Association of a Mutation in LACC1 With a Monogenic Form of Systemic Juvenile Idiopathic Arthritis by Wakil, Salma M., Monies, Dorota M., Abouelhoda, Mohamed, Al‐Tassan, Nada, Al‐Dusery, Haya, Naim, Ewa A., Al‐Younes, Banan, Shinwari, Jameela, Al‐Mohanna, Futwan A., Meyer, Brian F., Al‐Mayouf, Sulaiman

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  3. 3
    Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

    Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families by Alazami, Anas M., Patel, Nisha, Shamseldin, Hanan E., Anazi, Shamsa, Al-Dosari, Mohammed S., Alzahrani, Fatema, Hijazi, Hadia, Alshammari, Muneera, Aldahmesh, Mohammed A., Salih, Mustafa A., Faqeih, Eissa, Alhashem, Amal, Bashiri, Fahad A., Al-Owain, Mohammed, Kentab, Amal Y., Sogaty, Sameera, Al Tala, Saeed, Temsah, Mohamad-Hani, Tulbah, Maha, Aljelaify, Rasha F., Alshahwan, Saad A., Seidahmed, Mohammed Zain, Alhadid, Adnan A., Aldhalaan, Hesham, AlQallaf, Fatema, Kurdi, Wesam, Alfadhel, Majid, Babay, Zainab, Alsogheer, Mohammad, Kaya, Namik, Al-Hassnan, Zuhair N., Abdel-Salam, Ghada M.H., Al-Sannaa, Nouriya, Al Mutairi, Fuad, El Khashab, Heba Y., Bohlega, Saeed, Jia, Xiaofei, Nguyen, Henry C., Hammami, Rakad, Adly, Nouran, Mohamed, Jawahir Y., Abdulwahab, Firdous, Ibrahim, Niema, Naim, Ewa A., Al-Younes, Banan, Meyer, Brian F., Hashem, Mais, Shaheen, Ranad, Xiong, Yong, Abouelhoda, Mohamed, Aldeeri, Abdulrahman A., Monies, Dorota M., Alkuraya, Fowzan S.

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  4. 4
    Elbasvir/grazoprevir in children aged 3-18 years with chronic HCV genotype 1 or 4 infection: a pharmacokinetic modeling study

    Elbasvir/grazoprevir in children aged 3-18 years with chronic HCV genotype 1 or 4 infection: a pharmacokinetic modeling study by Gonzalez-Peralta, Regino P, Wirth, Stefan, Squires, Robert H, Mutschler, Frauke, Lang, Thomas, Pawlowska, Malgorzata, Sluzewski, Wojciech, Majda-Stanislawska, Ewa, Fischler, Bjorn, Balistreri, William F, Jonas, Maureen M, Blondet, Niviann, Rosenthal, Philip, Alkhouri, Naim, Romero, Rene, Grandhi, Anjana, Castronuovo, Patricia, Caro, Luzelena, Du, Lihong, Rosenbloom, Daniel I S, Haber, Barbara A

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