| A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis MY Ahmed, A Al-Khayat, F Al-Murshedi, A Al-Futaisi, BA Chioza, ... Brain 140 (3), 547-554, 2017 | 87 | 2017 |
| PLPHP deficiency: clinical, genetic, biochemical, and mechanistic insights DL Johnstone, HH Al-Shekaili, M Tarailo-Graovac, NI Wolf, AS Ivy, ... Brain 142 (3), 542-559, 2019 | 74 | 2019 |
| Reanalysis of exome sequencing data of intellectual disability samples: yields and benefits M Al‐Nabhani, S Al‐Rashdi, F Al‐Murshedi, A Al‐Kindi, K Al‐Thihli, ... Clinical genetics 94 (6), 495-501, 2018 | 74 | 2018 |
| A clinician's approach to peripheral neuropathy P Siao, M Kaku Seminars in neurology 39 (05), 519-530, 2019 | 71 | 2019 |
| International survey of critically ill children with acute neurologic insults: the prevalence of acute critical neurological disease in children: a global epidemiological … EL Fink, PM Kochanek, RC Tasker, J Beca, MJ Bell, RSB Clark, ... Pediatric Critical Care Medicine 18 (4), 330-342, 2017 | 65 | 2017 |
| Predictive value of clinical and EEG features in the diagnosis of stroke and hypoxic ischemic encephalopathy in neonates with seizures MF Rafay, MA Cortez, GA deVeber, C Tan-Dy, A Al-Futaisi, W Yoon, ... Stroke 40 (7), 2402-2407, 2009 | 64 | 2009 |
| Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases E Perenthaler, A Nikoncuk, S Yousefi, WM Berdowski, M Alsagob, I Capo, ... Acta Neuropathologica 139, 415-442, 2020 | 49 | 2020 |
| Vincristine‐induced neuropathy in pediatric patients with acute lymphoblastic leukemia in Oman: Frequent autonomic and more severe cranial nerve involvement HF Nazir, A AlFutaisi, M Zacharia, M Elshinawy, ST Mevada, A Alrawas, ... Pediatric blood & cancer 64 (12), e26677, 2017 | 45 | 2017 |
| Evaluation children with global developmental delay: A prospective study at Sultan Qaboos University Hospital, Oman R Koul, M Al-Yahmedy, A Al-Futaisi Oman medical journal 27 (4), 310, 2012 | 42 | 2012 |
| Prospective study of children with Guillain-Barre syndrome RL Koul, A Alfutaisi The Indian Journal of Pediatrics 75, 787-790, 2008 | 34 | 2008 |
| Clinical characteristics of childhood guillain-barré syndrome R Koul, A Al-Futaisi, A Chacko, M Fazalullah, S Al Nabhani, S Al-Awaidy, ... Oman Medical Journal 23 (3), 158, 2008 | 31 | 2008 |
| Learning disabilities: Opportunities and challenges in Oman A Al-Mahrezi, A Al-Futaisi, W Al-Mamari Sultan Qaboos University Medical Journal 16 (2), e129, 2016 | 27 | 2016 |
| Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation AM Al-Futaisi, MN Al-Kindi, AM Al-Mawali, RL Koul, S Al-Adawi, ... Pediatric neurology 46 (2), 89-93, 2012 | 26 | 2012 |
| Comorbidity of learning disorders and attention deficit hyperactivity disorder in a sample of Omani schoolchildren WS Al-Mamari, MM Emam, AM Al-Futaisi, AM Kazem Sultan Qaboos University Medical Journal 15 (4), e528, 2015 | 25 | 2015 |
| Rituximab in severe seronegative juvenile myasthenia gravis: review of the literature R Koul, A Al Futaisi, R Abdwani Pediatric neurology 47 (3), 209-212, 2012 | 25 | 2012 |
| Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with hyperintense brainstem nuclei on magnetic resonance imaging: new finding in three siblings R Koul, R Jain, A Chacko, A Alfutaisi, J Hashim, J Chacko Journal of child neurology 21 (6), 523-525, 2006 | 24 | 2006 |
| TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia LC Tábara, F Al-Salmi, R Maroofian, AM Al-Futaisi, F Al-Murshedi, ... Brain 145 (9), 3095-3107, 2022 | 19 | 2022 |
| Hidden focal EEG seizures during prolonged suppressions and high-amplitude bursts in early infantile epileptic encephalopathy A Al-Futaisi, B Banwell, A Ochi, J Hew, B Chu, M Oishi, H Otsubo Clinical neurophysiology 116 (5), 1113-1117, 2005 | 19 | 2005 |
| Nonketotic hyperglycinemia: two case reports and review RP Poothrikovil, K Al Thihli, A Al Futaisi, F Al Murshidi The Neurodiagnostic Journal 59 (3), 142-151, 2019 | 17 | 2019 |
| Spectrum of paediatric lysosomal storage disorders in Oman AA Al-Maawali, SN Joshi, RL Koul, AA Al-Maawali, HS Al-Sedari, ... Sultan Qaboos University Medical Journal 12 (3), 295, 2012 | 15 | 2012 |
Roshan KoulInstitute of Liver and Biliary SciencesVerified email at squ.edu.om
