Vitamin D supplementation to prevent vitamin D deficiency for children with epilepsy: Randomized pragmatic trial protocol von Khalifah, Reem Al, Hudairi, Abrar, Homyani, Doua Al, Hamad, Muddathir H., Bashiri, Fahad A.

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International alliance and AGREE-ment of 71 clinical practice guidelines on the management of critical care patients with COVID-19: a living systematic review von Amer, Yasser S., Titi, Maher A., Godah, Mohammad W., Wahabi, Hayfaa A., Hneiny, Layal, Abouelkheir, Manal Mohamed, Hamad, Muddathir H., ElGohary, Ghada Metwally, Hamouda, Mohamed Ben, Ouertatani, Hella, Velasquez-Salazar, Pamela, Acosta-Reyes, Jorge, Alhabib, Samia M., Esmaeil, Samia Ahmed, Fedorowicz, Zbys, Zhang, Ailing, Chen, Zhe, Liptrott, Sarah Jayne, Frungillo, Niccolò, Jamal, Amr A., Almustanyir, Sami A., Dieyi, Newman Ugochukwu, Powell, John, Hon, Katrina J., Alzeidan, Rasmieh, Azzo, Majduldeen, Zambrano-Rico, Sara, Ramirez-Jaramillo, Paulina, Florez, Ivan D.

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An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families von Koko, Mahmoud, Yahia, Ashraf, Elsayed, Liena E., Hamed, Ahlam A., Mohammed, Inaam N., Elseed, Maha A., Hamad, Muddathir H. A., Babai, Arwa M., Siddig, Rayan A., Abd Allah, Amal S. I., Mohamed, Mayada, EL‐Amin, Melka, Esteves, Typhaine, Altmüller, Janine, Toliat, Mohammad Reza, Thiele, Holger, Nürnberg, Peter, Salih, Mustafa A., Ahmed, Ammar E., Lerche, Holger, Stevanin, Giovanni

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Appraisal of clinical practice guidelines for the management of attention deficit hyperactivity disorder (ADHD) using the AGREE II Instrument: A systematic review von Amer, Yasser Sami, Al-Joudi, Haya Faisal, Varnham, Jeremy L, Bashiri, Fahad A, Hamad, Muddathir Hamad, Al Salehi, Saleh M, Daghash, Hadeel Fakhri, Albatti, Turki Homod

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First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient von Alsagob, Maysoon, Salih, Mustafa A, Hamad, Muddathir H A, Al-Yafee, Yusra, Al-Zahrani, Jawaher, Al-Bakheet, Albandary, Nester, Michael, Sakati, Nadia, Wakil, Salma M, AlOdaib, Ali, Colak, Dilek, Kaya, Namik

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Vitamin D Supplementation for Children with Epilepsy on Antiseizure Medications: A Randomized Controlled Trial von Bashiri, Fahad A, Hudairi, Abrar, Hamad, Muddathir H, Al-Sulimani, Lujain K, Al Homyani, Doua, Al Saqabi, Dimah, Kentab, Amal Y, Al Khalifah, Reem A

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Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes von Himmelreich, Nastassja, Bertoldi, Mariarita, Alfadhel, Majid, Alghamdi, Malak Ali, Anikster, Yair, Bao, Xinhua, Bashiri, Fahad A., Zeev, Bruria Ben, Bisello, Giovanni, Ceylan, Ahmet Cevdet, Chien, Yin-Hsiu, Choy, Yew Sing, Elsea, Sarah H., Flint, Lisa, García-Cazorla, Àngels, Gijavanekar, Charul, Gümüş, Emel Yılmaz, Hamad, Muddathir H., Hişmi, Burcu, Honzik, Tomas, Hübschmann, Oya Kuseyri, Hwu, Wuh-Liang, Ibáñez-Micó, Salvador, Jeltsch, Kathrin, Juliá-Palacios, Natalia, Kasapkara, Çiğdem Seher, Kurian, Manju A., Kusmierska, Katarzyna, Liu, Ning, Ngu, Lock Hock, Odom, John D., Ong, Winnie Peitee, Opladen, Thomas, Oppeboen, Mari, Pearl, Phillip L., Pérez, Belén, Pons, Roser, Rygiel, Agnieszka Magdalena, Shien, Tan Ee, Spaull, Robert, Sykut-Cegielska, Jolanta, Tabarki, Brahim, Tangeraas, Trine, Thöny, Beat, Wassenberg, Tessa, Wen, Yongxin, Yakob, Yusnita, Yin, Jasmine Goh Chew, Zeman, Jiri, Blau, Nenad

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

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Developmental and/or epileptic encephalopathy with spike-and-wave activation in sleep in Saudi Arabia: Electroclinical, etiologic, genetic, and outcome multicenter study von Alsini, Hanin, Alghamdi, Abdulaziz, Alshafi, Shatha, Hundallah, Khalid, Almehmadi, Sameer, Alsowat, Daad, Al-Yamani, Suad, Almuzaini, Hanin, Alwadie, Ali, Al-Otaibi, Ali, Jad, Lamyaa, Almadhi, Asma, Bashiri, Fahad, Kentab, Amal, Hamad, Muddathir H, Baarmah, Duaa, Alrifaie, Mohammed, Almuqbel, Mohammed, Baradie, Raidah Al, Mir, Ali, Jan, Mohammed, Muthaffar, Osama, Aljabri, Mohammed, Ali, Elsayed, Saeed, Mohammed, Matar, Abeer, Tabarki, Brahim

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

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

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

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The natural history of infantile neuroaxonal dystrophy von Altuame, Fadie D., Foskett, Gretchen, Atwal, Paldeep S., Endemann, Sarah, Midei, Mark, Milner, Peter, Salih, Mustafa A., Hamad, Muddathir, Al-Muhaizea, Mohammad, Hashem, Mais, Alkuraya, Fowzan S.

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Appraisal of clinical practice guidelines for the management of attention deficit hyperactivity disorder von Amer, Yasser Sami, Al-Joudi, Haya Faisal, Varnham, Jeremy L, Bashiri, Fahad A, Hamad, Muddathir Hamad, Al Salehi, Saleh M, Daghash, Hadeel Fakhri, Albatti, Turki Homod

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

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Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes von Himmelreich, Nastassja, Bertoldi, Mariarita, Alfadhel, Majid, Alghamdi, Malak Ali, Anikster, Yair, Bao, Xinhua, Bashiri, Fahad A., Zeev, Bruria Ben, Bisello, Giovanni, Ceylan, Ahmet Cevdet, Chien, Yin-Hsiu, Choy, Yew Sing, Elsea, Sarah H., Flint, Lisa, García-Cazorla, Àngels, Gijavanekar, Charul, Gümüş, Emel Yılmaz, Hamad, Muddathir H., Hişmi, Burcu, Honzik, Tomas, Kuseyri Hübschmann, Oya, Hwu, Wuh-Liang, Ibáñez-Micó, Salvador, Jeltsch, Kathrin, Juliá-Palacios, Natalia, Kasapkara, Çiğdem Seher, Kurian, Manju A., Kusmierska, Katarzyna, Liu, Ning, Ngu, Lock Hock, Odom, John D., Ong, Winnie Peitee, Opladen, Thomas, Oppeboen, Mari, Pearl, Phillip L., Pérez, Belén, Pons, Roser, Rygiel, Agnieszka Magdalena, Shien, Tan Ee, Spaull, Robert, Sykut-Cegielska, Jolanta, Tabarki, Brahim, Tangeraas, Trine, Thöny, Beat, Wassenberg, Tessa, Wen, Yongxin, Yakob, Yusnita, Yin, Jasmine Goh Chew, Zeman, Jiri, Blau, Nenad

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Childhood absence epilepsy: Electro-clinical manifestations, treatment options, and outcome in a tertiary educational center von Bashiri, Fahad A., Al dosari, Abdullah, Hamad, Muddathir H., Kentab, Amal Y., Alwadei, Ali H.

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Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies von Salih, Mustafa A., Hamad, Muddathir H., Savarese, Marco, Alorainy, Ibrahim A., Al-Jarallah, Abdullah S., Alkhalidi, Hisham, AlQudairy, Hanan, Albader, Anoud, Alotaibi, Amal Jahz, Alsagob, Maysoon, Al-Bakheet, Albandary, Colak, Dilek, Udd, Bjarne, Kaya, Namik

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

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Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center von Kentab, Amal Y, Al Bulayhi, Shumukh, Hamad, Muddathir H, Al Wadei, Ali, Bashiri, Fahad A

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