Search Results - Hamad, Aleidi

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  1. 1
    Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report

    Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report by Al Mutairi, Fuad, Alkhalaf, Randa, Alkhorayyef, Abdullah, Alroqi, Fayhan, Yusra, Alyafee, Umair, Muhammad, Nouf, Fetaini, Khan, Amjad, Meshael, Alharbi, Hamad, Aleidi, Monira, Alaujan, Asiri, Abdulaziz, Alhamoudi, Kheloud M, Alfadhel, Majid

    Published in BMC pulmonary medicine
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  2. 2
    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype

    Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype by Al Tuwaijri, Abeer, Alyafee, Yusra, Umair, Muhammad, Alsubait, Arwa, Alharbi, Mashael, AlEidi, Hamad, Ballow, Mariam, Aldrees, Mohammed, Alam, Qamre, Al Abdulrahman, Abdulkareem, Alrifai, Muhammad Talal, Alfadhel, Majid

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  3. 3
    The Relation Between Body Mass Index and Musculoskeletal Injury

    The Relation Between Body Mass Index and Musculoskeletal Injury by Alangari, Abdulaziz A, Almutairi, Mohammed M, Alrrajeh, Abdulmalik M, Aleidi, Mohammad A, Alqarni, Mohammed A, Almeneif, Hesham A, Alolaywi, Hamad K, Almuklass, Awad M

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  4. 4
    Research Trend in The Inhibition of Transient Receptor Potential Vanilloid 1 (TRPV1): Bibliometric Analysis and Visualization

    Research Trend in The Inhibition of Transient Receptor Potential Vanilloid 1 (TRPV1): Bibliometric Analysis and Visualization by Aleidi, Shereen M., Harb, Amani A., Dahabiyeh, Lina A., AL-Iede, Montaha, Hamad, Islam, Alshaer, Walhan, Almasri, Ihab M., Bustanji, Yasser

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