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Page 1
TMEM63C mutations cause mitochondrial morphology defects and underlie hereditary spastic paraplegia.
Brain. 2022 Sep 14;145(9):3095-3107. doi: 10.1093/brain/awac123.
Brain. 2022.
PMID: 35718349
Free PMC article.
Pituitary Adenoma Prevalence and Characteristics of Omani Patients: A Single Center Experience.
Al Futaisi AM, Al Marzouqi AM, Al Abri MA, Al Riyami MZ.
Al Futaisi AM, et al.
Oman Med J. 2024 Jan 31;39(1):e589. doi: 10.5001/omj.2024.44. eCollection 2024 Jan.
Oman Med J. 2024.
PMID: 38567166
Free PMC article.
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Novel mutation of GLRA1 in Omani families with hyperekplexia and mild mental retardation.
Al-Futaisi AM, Al-Kindi MN, Al-Mawali AM, Koul RL, Al-Adawi S, Al-Yahyaee SA.
Al-Futaisi AM, et al.
Pediatr Neurol. 2012 Feb;46(2):89-93. doi: 10.1016/j.pediatrneurol.2011.11.008.
Pediatr Neurol. 2012.
PMID: 22264702
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Subcutaneous administration of testosterone. A pilot study report.
Al-Futaisi AM, Al-Zakwani IS, Almahrezi AM, Morris D.
Al-Futaisi AM, et al.
Saudi Med J. 2006 Dec;27(12):1843-6.
Saudi Med J. 2006.
PMID: 17143361
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Spectrum of paediatric lysosomal storage disorders in oman.
Al-Maawali AA, Joshi SN, Koul RL, Al-Maawali AA, Al-Sedari HS, Al-Amri BM, Al-Futaisi AM.
Al-Maawali AA, et al. Among authors: al futaisi am.
Sultan Qaboos Univ Med J. 2012 Aug;12(3):295-9. doi: 10.12816/0003142. Epub 2012 Jul 15.
Sultan Qaboos Univ Med J. 2012.
PMID: 22912921
Free PMC article.
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Comorbidity of Learning Disorders and Attention Deficit Hyperactivity Disorder in a Sample of Omani Schoolchildren.
Al-Mamari WS, Emam MM, Al-Futaisi AM, Kazem AM.
Al-Mamari WS, et al. Among authors: al futaisi am.
Sultan Qaboos Univ Med J. 2015 Nov;15(4):e528-33. doi: 10.18295/squmj.2015.15.04.015. Epub 2015 Nov 23.
Sultan Qaboos Univ Med J. 2015.
PMID: 26629382
Free PMC article.
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