Reanalysis of exome sequencing data of intellectual disability samples: Yields and benefits von Al‐Nabhani, Maryam, Al‐Rashdi, Samiya, Al‐Murshedi, Fathiya, Al‐Kindi, Adila, Al‐Thihli, Khalid, Al‐Saegh, Abeer, Al‐Futaisi, Amna, Al‐Mamari, Watfa, Zadjali, Fahad, Al‐Maawali, Almundher

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Missense mutations in SLC25A1 are associated with congenital myasthenic syndrome type 23 von Al‐Futaisi, Amna, Ahmad, Faraz, Al‐Kasbi, Ghalia, Al‐Thihli, Khalid, Koul, Roshan, Al‐Maawali, Almundher

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Variability of non‐lethal Fowler syndrome phenotype associated with FLVCR2 variants von Al‐Murshedi, Fathiya, Mirza, Hassan, Al‐Saegh, Abeer, Al‐Nabhani, Maryam, Al‐Shabibi, Saud, Baawain, Saleh, Al‐Futaisi, Amna, Al‐Shehhi, Wafaa, Al‐Maawali, Almundher

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Telemedicine in the era of COVID-19 and beyond : a new horizon von Alsaffar, Hussain, Almamari, Watfa, Al Futaisi, Amna

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Transient response to high‐dose niacin therapy in a patient with NAXE deficiency von Al‐Amrani, Fatema, Al‐Thihli, Khalid, Al‐Ajmi, Eiman, Al‐Futaisi, Amna, Al‐Murshedi, Fathiya

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Pediatric migraines: A comprehensive review and perspectives on diagnosis and treatment von Amna Al-Futaisi

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Inappropriate Laughter in a Patient with Hypothalamic Hamartoma von Ahmad , Faraz, Elmanzalawy , Alaa, Al Kalbani , Faris, Al Futaisi , Amna

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Rituximab in Severe Seronegative Juvenile Myasthenia Gravis: Review of the Literature von Koul, Roshan, MD, Al Futaisi, Amna, MD, Abdwani, Reem, MD

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Comorbidity of Learning Disorders and Attention Deficit Hyperactivity Disorder in a Sample of Omani Schoolchildren von Al-Mamari , Watfa S, Al-Futaisi , Amna M, Emam , Mahmoud M, Kazem , Ali M

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Tuberous sclerosis complex with renal stones and distal renal tubular acidosis: Case report and literature review von Al Omairi, Anwar, Al Futaisi, Amna

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Case report: Cyclosporine A-induced extrapyramidal syndrome following hematopoietic stem cell transplantation von Al-Amrani, Fatema, Al Rawas, Abdulhakeem, Al-Ajmi, Eiman, Al Futaisi, Amna

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Expanding the clinical spectrum of cytosolic phosphoenolpyruvate carboxykinase deficiency: novel PCK1 variants in four Arabian Gulf families von Al Busaidi, Marwa, Mohamed, Feda E, Al-Ajmi, Eiman, Al Hashmi, Nadia, Al-Thihli, Khalid, Al Futaisi, Amna, Al Mamari, Watfa, Al-Murshedi, Fathiya, Al-Jasmi, Fatma

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The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families von Al-Kasbi, Ghalia, Al-Murshedi, Fathiya, Al-Kindi, Adila, Al-Hashimi, Nadia, Al-Thihli, Khalid, Al-Saegh, Abeer, Al-Futaisi, Amna, Al-Mamari, Watfa, Al-Asmi, Abdullah, Bruwer, Zandre, Al-Kharusi, Khalsa, Al-Rashdi, Samiya, Zadjali, Fahad, Al-Yahyaee, Said, Al-Maawali, Almundher

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The Parental and Children Report of the Prevalence of Depressive Symptoms in Children and Adolescents Amid the COVID-19 Pandemic: A Cross-Sectional Study From Oman von Zadjali, Fahad, Al-Futaisi, Amna, Al-Hosni, Amira, Al-Huseini, Salim, Crommelin, Maarten, Mirza, Hassan

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Recessive mutations in SCYL2 cause a novel syndromic form of arthrogryposis in humans von Seidahmed, Mohammed Zain, Al-Kindi, Adila, Alsaif, Hessa S., Miqdad, Abeer, Alabbad, Nasser, Alfifi, Abdallah, Abdelbasit, Omer Bashir, Alhussein, Khalid, Alsamadi, Abdulmohsen, Ibrahim, Niema, Al-Futaisi, Amna, Al-Maawali, Almundher, Alkuraya, Fowzan S.

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Corrigendum: Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendations von Bashiri, Fahad A., Hundallah, Khaled, Abukhaled, Musaad, Alyahya, Mossaed Mohammed, Al Futaisi, Amna, Alshowaeir, Daniah, Al Tawari, Asmaa, Abdullah, Shaker, Maaz, Ata Ur Rehman, AlShamsi, Eman Taryam, Alshuaibi, Walaa, Alotaibi, Faisal, Aldhalaan, Hesham

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Perception about telemedicine services among parents of children with neurodevelopmental disorders in a specialised tertiary centre in Oman von B Idris, Ahmed, Al-Mamari, Watfa, Al Humaidi, Taif Saud, Al Ma'ashri, Kawther Abdullah, Alhabsi, Ahmed, Jalees, Saquib, Gaber, Ahlam, Al-Jabri, Muna, Islam, M Mazharul, Al-Futaisi, Amna

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Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendations von Bashiri, Fahad A, Hundallah, Khaled, Abukhaled, Musaad, Alyahya, Mossaed Mohammed, Al Futaisi, Amna, Alshowaeir, Daniah, Al Tawari, Asmaa, Abdullah, Shaker, Maaz, Ata Ur Rehman, AlShamsi, Eman Taryam, Alshuaibi, Walaa, Alotaibi, Faisal, Aldhalaan, Hesham

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Assessment of quality of life in children with epilepsy in Oman von Alnaamani, Asia, Ahmad, Faraz, Al-Saadoon, Muna, Rizvi, Syed Gauhar Alam, Al-Futaisi, Amna

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Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement von Bashiri, Fahad A., Hundallah, Khalid, Al-Baradie, Raidah, Al-Otaibi, Ali, Ismayl, Omar, AlMalik, Mohamed Elhadi, Muthaffar, Osama Y., Futaisi, Amna Al, Kurdi, Daniah, Tawari, Asmaa Al, AlSowat, Daad, Shafi, Shatha AL, Ali, Ayman, AlHajjar, Lynn M., Aldakhil, Abdullah

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