Canlyniadau Chwilio - Muddathir H. Hamad
- Dangos 1 - 9 canlyniadau o 9
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1
Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene gan Mohammed F. Alosaimi, Mohammed F. Alosaimi, Muddathir H. Hamad, Muneera J. AlShammari, Dima Z. Jamjoom, Najd S. Musibeeh
Cyhoeddwyd 2023Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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2
Prevalence and Related Risk Factors of Vitamin D Deficiency in Saudi Children with Epilepsy gan Reem Al Khalifah, Muddathir H. Hamad, Abrar Hudairi, Lujain K. Al-Sulimani, Doua Al Homyani, Dimah Al Saqabi, Fahad A. Bashiri
Cyhoeddwyd 2022Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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3
Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital gan Fahad A. Bashiri, Rawan AlSheikh, Muddathir H. Hamad, Hamad Alsheikh, Rana Abdullah Alsheikh, Amal Kentab, Najd AlTheeb, Malak Alghamdi
Cyhoeddwyd 2023Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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4
Impact of the Coronavirus Disease 2019 pandemic on an ongoing pragmatic pediatric clinical trial gan Abrar F Hudairi, Fahad A Bashiri, Lujain K AL-Sulimani, Dimah AlSaqabi, Mohamed A A. Mohamed, Muddathir H Hamad, Reem Al Khalifah
Cyhoeddwyd 2021Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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5
Vitamin D Supplementation for Children with Epilepsy on Antiseizure Medications: A Randomized Controlled Trial gan Fahad A. Bashiri, Abrar Hudairi, Muddathir H. Hamad, Lujain K. Al-Sulimani, Doua Al Homyani, Dimah Al Saqabi, Amal Y. Kentab, Reem A. Al Khalifah
Cyhoeddwyd 2024Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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6
Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital gan 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
Cyhoeddwyd 2022Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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7
Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia gan 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
Cyhoeddwyd 2024Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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8
Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia gan 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
Cyhoeddwyd 2020Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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9
Adapting evidence-based clinical practice guidelines for people with attention deficit hyperactivity disorder in Saudi Arabia: process and outputs of a national initiative gan 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
Cyhoeddwyd 2021Rhif Galw: Llwytho...Connect to this object online.
Wedi'i leoli: Llwytho...
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