Hasil Pencarian - Mona O. El Ruby

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  1. 1
    Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls

    Association between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls... oleh Nora N. Esmaiel, Engy A. Ashaat, Ghada M. Al-Ettribi, Alaaeldin Fayez, Sonia A. Alsaiedi, Mona O. El Ruby

    Diterbitkan 2023-04-01
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  2. 2
    miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients

    miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian pat... oleh Alaaeldin G. Fayez, Nora N. Esmaiel, Sohair M. Salem, Engy A. Ashaat, Sonia A. El-Saiedi, Mona O. El Ruby

    Diterbitkan 2022-09-01
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  3. 3
    Altered Adaptive Cellular Immune Function in a Group of Egyptian Children with Autism

    Altered Adaptive Cellular Immune Function in a Group of Egyptian Children with Autism oleh Engy A. Ashaat, Khaled H. Taman, Naglaa Kholoussi, Mona O. El Ruby, Moushira Erfan Zaki, Maged A. El Wakeel, Neveen A. Ashaat, Samira Ismail Ibrahim

    Diterbitkan 2017-10-01
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  4. 4
    Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

    Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children oleh Azza K. Abdel Megeid, Miral M. Refeat, Engy A. Ashaat, Ghada El-Kamah, Sonia A. El-Saiedi, Mona M. Elfalaki, Mona O. El Ruby, Khalda S. Amr

    Diterbitkan 2022-09-01
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  5. 5
    Correlating SFTPC gene variants to interstitial lung disease in Egyptian children

    Correlating SFTPC gene variants to interstitial lung disease in Egyptian children oleh Azza K. Abdel Megeid, Miral M. Refeat, Engy A. Ashaat, Ghada El-Kamah, Sonia A. El-Saiedi, Mona M. Elfalaki, Mona O. El Ruby, Khalda S. Amr

    Diterbitkan 2022-08-01
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  6. 6
    New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects

    New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects oleh Alaaeldin G. Fayez, PhD, Nora N. Esmaiel, PhD, Engy A. Ashaat, MD, Miral M. Refeat, PhD, Randa S. Lotfy, PhD, Haiam Abdel Raouf, PhD, Mona O. El Ruby, MD

    Diterbitkan 2023-12-01
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  7. 7
    Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature

    Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature oleh Mona K. Mekkawy, Alaa K. Kamel, Manal M. Thomas, Engy A. Ashaat, Maha S. Zaki, Ola M. Eid, Samira Ismail, Saida A. Hammad, Hisham Megahed, Heba ElAwady, Khaled M. Refaat, Shymaa Hussien, Nivine Helmy, Sally G. Abd Allah, Amal M. Mohamed, Mona O. El Ruby

    Diterbitkan 2021-02-01
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