Hasil Pencarian - Muddathir H Hamad

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  1. 1
    Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene

    Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene oleh Mohammed F. Alosaimi, Mohammed F. Alosaimi, Muddathir H. Hamad, Muneera J. AlShammari, Dima Z. Jamjoom, Najd S. Musibeeh

    Diterbitkan 2023-09-01
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  2. 2
    Prevalence and Related Risk Factors of Vitamin D Deficiency in Saudi Children with Epilepsy

    Prevalence and Related Risk Factors of Vitamin D Deficiency in Saudi Children with Epilepsy oleh Reem Al Khalifah, Muddathir H. Hamad, Abrar Hudairi, Lujain K. Al-Sulimani, Doua Al Homyani, Dimah Al Saqabi, Fahad A. Bashiri

    Diterbitkan 2022-11-01
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  3. 3
    Genotype–Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital

    Genotype–Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital oleh Fahad A. Bashiri, Rawan AlSheikh, Muddathir H. Hamad, Hamad Alsheikh, Rana Abdullah Alsheikh, Amal Kentab, Najd AlTheeb, Malak Alghamdi

    Diterbitkan 2023-08-01
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  4. 4
    Impact of the Coronavirus Disease 2019 pandemic on an ongoing pragmatic pediatric clinical trial

    Impact of the Coronavirus Disease 2019 pandemic on an ongoing pragmatic pediatric clinical trial oleh Abrar F Hudairi, Fahad A Bashiri, Lujain K AL-Sulimani, Dimah AlSaqabi, Mohamed A A. Mohamed, Muddathir H Hamad, Reem Al Khalifah

    Diterbitkan 2021-01-01
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  5. 5
    Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital

    Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital oleh Khalid A. Alhasan, Walaa Alshuaibi, Muddathir H. Hamad, Suha Salim, Dima Z. Jamjoom, Aqeela H. Alhashim, Malak Ali AlGhamdi, Amal Y. Kentab, Fahad A. Bashiri

    Diterbitkan 2022-09-01
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  6. 6
    Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15)

    Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15) oleh Mohammed Z. Seidahmed, Muddathir H. Hamad, Albandary AlBakheet, Salah A. Elmalik, Abdulmajeed AlDrees, Jumanah Al-Sufayan, Ibrahim Alorainy, Ibrahim M. Ghozzi, Dilek Colak, Mustafa A. Salih, Namik Kaya

    Diterbitkan 2020-05-01
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  7. 7
    Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia

    Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia oleh Amal Y. Kentab, Amal Y. Kentab, Yara Alsalloum, Mai Labani, Abrar Hudairi, Muddathir H. Hamad, Dima Z. Jamjoom, Ali H. Alwadei, Ali H. Alwadei, Reem M. Alhammad, Fahad A. Bashiri, Fahad A. Bashiri

    Diterbitkan 2024-04-01
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  8. 8
    Mutation in GM2A Leads to a Progressive Chorea-Dementia Syndrome

    Mutation in GM2A Leads to a Progressive Chorea-Dementia Syndrome oleh Mustafa A. Salih, Mohammed Z. Seidahmed, Heba Y. El Khashab, Muddathir H. Hamad, Thomas M. Bosley, Sabrina Burn, Angela Myers, Megan L. Landsverk, Patricia L. Crotwell, Kaya Bilguvar, Shrikant Mane, Michael C. Kruer

    Diterbitkan 2015-07-01
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  9. 9
    Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia

    Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia oleh Fahad A. Bashiri, Sultan Al Johani, Muddathir H. Hamad, Amal Y. Kentab, Ali H. Alwadei, Khalid Hundallah, Hamdi H. Hasan, Walaa Alshuaibi, Lamyaa Jad, Muhammad Talal Alrifai, Abrar Hudairi, Rana Al Sheikh, Asma'a Alenizi, Nawaf A. Alharthi, Tayseer A. Abdelmagid, Duaa Ba-Armah, Mustafa A. Salih, Brahim Tabarki

    Diterbitkan 2020-10-01
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  10. 10
    Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative

    Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative oleh Fahad A. Bashiri, Turki H. Albatti, Muddathir H. Hamad, Haya F. Al-Joudi, Hadeel F. Daghash, Saleh M. Al-Salehi, Jeremy L. Varnham, Fatimah Alhaidar, Omar Almodayfer, Abdulkarim Alhossein, Hesham Aldhalaan, Yasser A. Ad-Dab’bagh, Nouf Al Backer, Waleed Altwaijri, Khalid Alburikan, Maysaa W. Buraik, Mohammad Ghaziuddin, Michael J. Nester, Hayfaa A. Wahabi, Samia Alhabib, Amr A. Jamal, Yasser S. Amer

    Diterbitkan 2021-02-01
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  11. 11
    Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome

    Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome oleh Malak Ali Alghamdi, Malak Ali Alghamdi, Hicham Benabdelkamel, Afshan Masood, Narjes Saheb Sharif-Askari, Mahmood Y. Hachim, Hamad Alsheikh, Muddathir H. Hamad, Mustafa A. Salih, Fahad A. Bashiri, Fahad A. Bashiri, Khalid Alhasan, Khalid Alhasan, Khalid Alhasan, Tarek Kashour, Pilar Guatibonza Moreno, Sabine Schröder, Vasiliki Karageorgou, Aida M. Bertoli-Avella, Hisham Alkhalidi, Dima Z. Jamjoom, Ibrahim A. Alorainy, Assim A. Alfadda, Assim A. Alfadda, Assim A. Alfadda, Rabih Halwani

    Diterbitkan 2022-06-01
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