The impact of maternal iron deficiency and iron deficiency anemia on child's health von Abu-Ouf, Noran M, Jan, Mohammed M

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Insight into Genetic Mutations of SZT2: Is It a Syndrome? von Muthaffar, Osama Y, Jan, Mohammed M. S, Alyazidi, Anas S, Alotibi, Taif K, Alsulami, Eman A

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Short-term effectiveness and side effects of ketogenic diet for drug-resistant epilepsy in children with genetic epilepsy syndromes von Muthaffar, Osama Y, Alyazidi, Anas S, Alsowat, Daad, Alasiri, Abdulaziz A, Albaradie, Raidah, Jad, Lamyaa A, Kayyali, Husam, Jan, Mohammed M S, Bamaga, Ahmed K, Alsubaie, Mohammed A, Daghistani, Rawan, Baeesa, Saleh S, Alaifan, Meshari A, Makraz, Abdelhakim, Alsharief, Abrar N, Naseer, Muhammad Imran

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Primary Stabbing “Ice-Pick” Headache von Mukharesh, Loulwah O., MBBS, Jan, Mohammed M.S., MBChB

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Neuroscience Forum: a scientific group on smartphones von Jan, Mohammed Ms

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Dental health of children with cerebral palsy von Jan, Basil M, Jan, Mohammed M

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Shuddering Attacks Are Not Related to Essential Tremor von Jan, Mohammed M. S.

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Whole exome sequencing reveals a homozygous nonsense mutation in HEXA gene leading to Tay-Sachs disease in Saudi Family von Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Jan, Mohammed Mohammed, Chaudhary, Adeel G, Al-Qahtani, Mohammad H

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Survey of non-resuscitation fluids administered during septic shock: a multicenter prospective observational study von Lindén-Søndersø, Anja, Jungner, Mårten, Spångfors, Martin, Jan, Mohammed, Oscarson, Adam, Choi, Sally, Kander, Thomas, Undén, Johan, Griesdale, Donald, Boyd, John, Bentzer, Peter

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Cerebral palsy: comprehensive review and update von Jan, Mohammed M S

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Association of ABO Blood Groups and Obesity in Patients With Diabetes Mellitus in King Abdulaziz University Hospital von Alqahtani, Reem Mohammed, Althagafi, Sohaib Essam, Althagafi, Aseel Ahmed, Alsayyad, Jalal Mohammed, Saeedi, Awatif Abdualaziz, Mishiming, Obadah Suhail, Yaghmour, Khaled A, Jan, Mohammed Anwar

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Lesion Type Analysis of Hemodialysis Patients Who Underwent Endovascular Management for Symptomatic Central Venous Disease von Aljarrah, Qusai, Allouh, Mohammed, Hallak, Amer H, Alghezawi, Shamikh E, Al-Omari, Mamoon, Elheis, Mwaffaq, Al-Jarrah, Mooath, Bakkar, Sohail, Aleshawi, Abdelwahab J, Al-Jarrah, Hussam, Ibrahim, Khalid S, Al Shishani, Jan Mohammed, Almukhtar, Aws

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Assessment of the etiologies and renal outcomes of rapidly progressive glomerulonephritis in pediatric patients at King Abdulaziz University Hospital, Jeddah, Saudi Arabia von Mosaad, Faisal G, Saggaf, Omar Mohammed, Aletwady, Khaled T, Mohammed Jan, Khaled Y, Al-Qarni, Khalid, Al-Harbi, Rakan S, Safdar, Osama Y

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A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family von Naseer, Muhammad Imran, Rasool, Mahmood, Jan, Mohammed M, Chaudhary, Adeel G, Pushparaj, Peter Natesan, Abuzenadah, Adel M, Al-Qahtani, Mohammad H

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Intravenous Methylprednisolone for Intractable Childhood Epilepsy von Almaabdi, Kholoud H., MBBS, Alshehri, Rawan O., MBBS, Althubiti, Areej A., MBBS, Alsharef, Zainab H., MBBS, Mulla, Sara N., MBBS, Alshaer, Dareen S., MBBS, Alfaidi, Nouf S., MBBS, Jan, Mohammed M., MBChB FRCPC

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Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic... von Naseer, Muhammad Imran, Abdulkareem, Angham Abdulrahman, Jan, Mohammed M., Chaudhary, Adeel G., Alharazy, Shatha, AlQahtani, Mohammad H.

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Neurological Examination of Difficult and Poorly Cooperative Children von Jan, Mohammed M. S.

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Pregabalin: Preliminary Experience in Intractable Childhood Epilepsy von Jan, Mohammed M.S., MBChB, Zuberi, Sobia A, Alsaihati, Bayan A

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Copy number variations in Saudi family with intellectual disability and epilepsy von Naseer, Muhammad I, Chaudhary, Adeel G, Rasool, Mahmood, Kalamegam, Gauthaman, Ashgan, Fai T, Assidi, Mourad, Ahmed, Farid, Ansari, Shakeel A, Zaidi, Syed Kashif, Jan, Mohammed M, Al-Qahtani, Mohammad H

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Genome wide analysis of novel copy number variations duplications/deletions of different epileptic patients in Saudi Arabia von Naseer, Muhammad Imran, Faheem, Muhammad, Chaudhary, Adeel G, Kumosani, Taha A, Al-Quaiti, Maha Mohsin, Jan, Mohammed M, Saleh Jamal, Hasan, Al-Qahtani, Mohammad H

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