Succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency: A rare and potentially fatal metabolic disease SC Grünert, W Foster, A Schumann, A Lund, C Pontes, S Roloff, ... Biochimie 183, 55-62, 2021 | 11 | 2021 |
Further delineation of METTL23‐associated intellectual disability M Almannai, O Obaid, E Faqeih, A Alasmari, MM Samman, H Pinz, ... American Journal of Medical Genetics Part A 182 (4), 785-791, 2020 | 4 | 2020 |
Neurological and extra-neurological clinical spectrum observed in pediatric patients with EMC1 gene variants identified by whole exome sequencing AA Peer-Zada, OA Obaid, MA Samman, A AlHashim, H AlAsmari, ... JBCGenetics 4 (2), 93-99, 2021 | 1 | 2021 |
Bilateral Glaucoma as Possible Additional Feature for PGAP3‐Associated Hyperphosphatasia O Obaid, R Batawi, H Alqurashi, T Ewis, AA Obaid Case Reports in Genetics 2024 (1), 3561555, 2024 | | 2024 |
Noninvasive high frequency oscillatory ventilation versus noninvasive positive pressure ventilation in preterm neonates after extubation: A randomized controlled trial WO Ahmed, ISH AbuSaif, SA Salaheldin, HE Hashem, OA Obaid, ... Journal of Neonatal-Perinatal Medicine, 1-10, 2023 | | 2023 |
The clinical spectrum and molecular heterogeneity of Succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency S Grünert, W Foster, A Schumann, L Allan, C Pontes, S Roloff, ... Monatsschrift Kinderheilkunde 170 (Suppl1), S13, 2021 | | 2021 |