Search Results - Ali Alasmari

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  1. 1
    Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy

    Mutations in UNC80, Encoding Part of the UNC79-UNC80-NALCN Channel Complex, Cause Autosomal-Recessive Severe Infantile Encephalopathy by Hanan E. Shamseldin, Eissa Faqeih, Ali Alasmari, Maha S. Zaki, Joseph G. Gleeson, Fowzan S. Alkuraya

    Published 2015
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  2. 2
    Bacterial Coinfections Increase Mortality of Severely Ill COVID-19 Patients in Saudi Arabia

    Bacterial Coinfections Increase Mortality of Severely Ill COVID-19 Patients in Saudi Arabia by Abdulaziz Alqahtani, Edrous Alamer, Mushtaq Ahmad Mir, Ali Alasmari, Mohammed Alshahrani, Mohammed Asiri, Irfan Ahmad, Abdulaziz Alhazmi, Abdullah Algaissi

    Published 2022
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  3. 3
    Application of artificial intelligence in nursing practice: a qualitative study of Jordanian nurses’ perspectives

    Application of artificial intelligence in nursing practice: a qualitative study of Jordanian nurses’ perspectives by Wesam Taher Almagharbeh, Hazem AbdulKareem Alfanash, Khaldoon Aied Alnawafleh, Amal Ali Alasmari, Faris A. Alsaraireh, Mutaz Dreidi, Abdulqadir J. Nashwan

    Published 2025
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  4. 4
    A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder

    A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder by Hanan E. Shamseldin, Ali Alasmari, Mohammed A. Salih, Manar Samman, Shahzad I. Mian, Tarfa Alshidi, Niema Ibrahim, Mais Hashem, Eissa Faqeih, Futwan Al‐Mohanna, Fowzan S. Alkuraya

    Published 2017
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  5. 5
    Zirconia Crowns for Primary Teeth: A Systematic Review and Meta-Analyses

    Zirconia Crowns for Primary Teeth: A Systematic Review and Meta-Analyses by Sara Douf Alzanbaqi, Rakan Mishaal Alogaiel, Mohammed Ali Alasmari, Ahmed Mohammed Al Essa, Layla Nizar Khogeer, Basim Salem Alanazi, Eyad Sami Hawsah, Ahmed Mohammed Shaikh, Maria Salem Ibrahim

    Published 2022
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  6. 6
    Clinical Impacts and Risk Factors for Central Line-Associated Bloodstream Infection: A Systematic Review

    Clinical Impacts and Risk Factors for Central Line-Associated Bloodstream Infection: A Systematic Review by Khadejah M Alshahrani, Afnan Z Alhuwaishel, Norah M Alangari, Malak A Asiri, Norah A Al-Shahrani, Amal Ali Alasmari, Osama Jamaan Mohammed Alzahrani, Abdulaziz Y Ayedh, Meshari Mari Qitmah

    Published 2023
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  7. 7
    Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation

    Biallelic Mutations in FUT8 Cause a Congenital Disorder of Glycosylation with Defective Fucosylation by Bobby G. Ng, Gege Xu, Nandini Chandy, Joan Steyermark, Deepali N. Shinde, Kelly Radtke, Kimiyo Raymond, Carlito B. Lebrilla, Ali Alasmari, Sharon F. Suchy, Zöe Powis, Eissa Faqeih, Susan A. Berry, David F. Kronn, Hudson H. Freeze

    Published 2018
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  8. 8
    Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance

    Mutations in FBXL4 Cause Mitochondrial Encephalopathy and a Disorder of Mitochondrial DNA Maintenance by Penelope E. Bonnen, John W. Yarham, Arnaud Besse, Ping Chun Wu, Eissa Faqeih, Ali Alasmari, Mohammad A.M. Saleh, Wafaa Eyaid, Alrukban Hadeel, Langping He, Frances J.D. Smith, Shu Yau, Eve M. Simcox, Satomi Miwa, Taraka Donti, Khaled K. Abu‐Amero, Lee‐Jun C. Wong, William J. Craigen, Brett H. Graham, Kenneth L. Scott, Robert McFarland, Robert W. Taylor

    Published 2013
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  9. 9
    Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies

    Expanding the clinical, allelic, and locus heterogeneity of retinal dystrophies by Nisha Patel, Mohammed A. Aldahmesh, Hisham Alkuraya, Shamsa Anazi, Hadeel Alsharif, Arif O. Khan, Asma Sunker, Saleh Al-mohsen, Emad B. Abboud, Sawsan R. Nowilaty, Mohammed Al‐Owain, Hamad Alzaidan, Bandar Al‐Saud, Ali Alasmari, Ghada M. H. Abdel‐Salam, Mohamed Abouelhoda, Firdous Abdulwahab, Niema Ibrahim, Ewa A. Naim, Banan Al‐Younes, Abeer Al‐Mostafa, Abdulelah AlIssa, Mais Hashem, Olga Buzovetsky, Yong Xiong, Dorota Monies, Nada Al Tassan, Ranad Shaheen, Selwa A.F. Al-Hazzaa, Fowzan S. Alkuraya

    Published 2015
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  10. 10
    Expanding the genetic heterogeneity of intellectual disability

    Expanding the genetic heterogeneity of intellectual disability by Shams Anazi, Sateesh Maddirevula, Vincenzo Salpietro, Yasmine T. Asi, Saud Alsahli, Amal Alhashem, Hanan E. Shamseldin, Fatema Alzahrani, Nisha Patel, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Nadia Alhashmi, Fathiya Al Murshedi, Adila Al Kindy, Ahmad Alshaer, Ahmed Al Rumayyan, Saeed Al Tala, Wesam Kurdi, Abdulaziz Alsaman, Ali Alasmari, Selina Banu, Tipu Sultan, Mohammed M. Saleh, Hisham Alkuraya, Mustafa A. Salih, Hesham Aldhalaan, Tawfeg Ben‐Omran, Fatima Al Musafri, Rehab Ali, Jehan Suleiman, Brahim Tabarki, Ayman W. El‐Hattab, Caleb Bupp, Majid Alfadhel, Nada Al Tassan, Dorota Monies, Stefan T. Arold, Mohamed Abouelhoda, Tammaryn Lashley, Henry Houlden, Eissa Faqeih, Fowzan S. Alkuraya

    Published 2017
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