MRI in sarcoglycanopathies: a large international cohort study G Tasca, M Monforte, J Díaz-Manera, G Brisca, C Semplicini, A D’Amico, ... Journal of Neurology, Neurosurgery & Psychiatry 89 (1), 72-77, 2018 | 71 | 2018 |
Biallelic inactivating variants in the GTPBP2 gene cause a neurodevelopmental disorder with severe intellectual disability AM Bertoli-Avella, JM Garcia-Aznar, O Brandau, F Al-Hakami, Z Yüksel, ... European Journal of Human Genetics 26 (4), 592-598, 2018 | 26 | 2018 |
Perception of pain during electromyography in children: A prospective study NM Alshaikh, JP Martinez, MC Pitt Muscle & Nerve 54 (3), 422-426, 2016 | 25 | 2016 |
Vitamin D in corticosteroid-naïve and corticosteroid-treated Duchenne muscular dystrophy: what dose achieves optimal 25 (OH) vitamin D levels? N Alshaikh, A Brunklaus, T Davis, SA Robb, R Quinlivan, P Munot, ... Archives of Disease in Childhood 101 (10), 957-961, 2016 | 17 | 2016 |
Consensus statement on the management of duchenne muscular dystrophy in Saudi Arabia during the coronavirus disease 2019 pandemic AK Bamaga, F Alghamdi, N Alshaikh, W Altwaijri, FA Bashiri, K Hundallah, ... Frontiers in pediatrics 9, 629549, 2021 | 14 | 2021 |
Type III spinal muscular atrophy mimicking muscular dystrophies AS Alsaman, NM AlShaikh Pediatric Neurology 48 (5), 363-366, 2013 | 12 | 2013 |
Hepatic encephalopathy coexists with acquired chronic hepatocerebral degeneration FZ Huang, X Hou, TQ Zhou, S Chen Neurosciences Journal 20 (3), 277-279, 2015 | 11 | 2015 |
A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19 F Alghamdi, N Alshaikh, AK Bamaga, FA Bashiri, K Hundullah, A Alshehri, ... Neurosciences Journal 25 (3), 230-237, 2020 | 4 | 2020 |
Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia AS AlSaman, F Al Ghamdi, AK Bamaga, N AlShaikh, M Al Muqbil, ... Frontiers in Pediatrics 10, 1020059, 2022 | 3 | 2022 |
Bridging the Gap: Parents’ Knowledge of Childhood Developmental Milestones and the Early Identification of Children With Developmental Delay HM Alghamdi, BA Altirkistani, RA Baatya, YO Marghalani, NM Alshaikh Cureus 15 (11), 2023 | 1 | 2023 |
Clinical and molecular characteristics of tectonic (TCTN1) gene-related Joubert syndrome in a Saudi boy BH Shirah, NM Alshaikh, A Shawli, MI Naseer Brain and Development 44 (4), 299-302, 2022 | | 2022 |
Erratum: A consensus statement on spinal muscular atrophy management in Saudi Arabia in the context of COVID-19. F Alghamdi, N Alshaikh, AK Bamaga, FA Bashiri, K Hundallah, A Alshehri, ... Neurosciences (Riyadh, Saudi Arabia) 25 (5), 440-440, 2020 | | 2020 |
Validation of gene causality for neurological disorders by WES/WGS analyses in a diagnostic setting AM Avella, Z Yueksel, H Yavuz, C Baldi, A Marais, JM Garcia-Aznar, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 524-526, 2019 | | 2019 |
BALANCING PLACEBO AND NOCEBO EFFECTS DURING ELECTROMYOGRAPHY IN CHILDREN REPLY NM Alshaikh, JP Martinez, MC Pitt MUSCLE & NERVE 54 (4), 812-812, 2016 | | 2016 |
Editor's Choice Articles TM Jenkins, JJP Alix, RH Kandler, PJ Shaw, CJ McDermott, NM Alshaikh, ... Perception, 2016 | | 2016 |
Vitamin D in corticosteroid treated Duchenne muscular dystrophy: What dose achieves serum 25OH vitamin D sufficiency? N Alshaikh, A Brunklaus, T Davis, S Robb, R Quinlivan, P Munot, ... Neuromuscular Disorders 25, S302, 2015 | | 2015 |
Clinical outcomes in a large cohort of boys and adolescents with Duchenne muscular dystrophy N Alshaikh, A Brunklaus, S Robb, R Quinlivan, P Munot, A Sarkozy, ... Neuromuscular Disorders 25, S302-S303, 2015 | | 2015 |