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2008 | 1 |
2022 | 1 |
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Page 1
Lunapark deficiency leads to an autosomal recessive neurodevelopmental phenotype with a degenerative course, epilepsy and distinct brain anomalies.
Brain Commun. 2023 Aug 17;5(5):fcad222. doi: 10.1093/braincomms/fcad222. eCollection 2023.
Brain Commun. 2023.
PMID: 37794925
Free PMC article.
Association of sodium voltage-gated channel genes polymorphisms with epilepsy risk and prognosis in the Saudi population.
Alghamdi MA, Al-Eitan LN, Asiri A, Rababa'h DM, Alqahtani SA, Aldarami MS, Alsaeedi MA, Almuidh RS, Alzahrani AA, Sakah AH, El Nashar EM, Otaif MY, Abdel Ghaffar NF.
Alghamdi MA, et al. Among authors: otaif my.
Ann Med. 2022 Dec;54(1):1938-1951. doi: 10.1080/07853890.2022.2096257.
Ann Med. 2022.
PMID: 35801810
Free PMC article.
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Vanishing white matter in Saudi Arabia.
Otaif MY, Al-Muhaizea MA, Al-Jofan F, Al-Dhalaan H.
Otaif MY, et al.
Neurosciences (Riyadh). 2008 Oct;13(4):433-6.
Neurosciences (Riyadh). 2008.
PMID: 21063376
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