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Metabolic and other morbid complications in congenital generalized lipodystrophy type 4.
Am J Med Genet A. 2024 Jun;194(6):e63533. doi: 10.1002/ajmg.a.63533. Epub 2024 Jan 17.
Am J Med Genet A. 2024.
PMID: 38234231
Establishment of diagnostic reference levels in computed tomography in two large hospitals in Oman.
Bouchareb Y, Al-Maimani A, Al-Balushi AY, Al-Kalbani M, Al-Maskari H, Al-Dhuhli H, Al-Kindi F.
Bouchareb Y, et al. Among authors: al maimani a.
Radiat Prot Dosimetry. 2023 Oct 18;199(17):2148-2155. doi: 10.1093/rpd/ncad225.
Radiat Prot Dosimetry. 2023.
PMID: 37594414
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Distal Arthrogryposis with Impaired Proprioception and Touch: A Novel Variant in PIEZO2 Gene in Omani Patients and a Genotype-Phenotype Review from a Single-Center Experience.
Al Balushi A, Al Hinai M, Al Hosni A, Al Amrani F, Al Maimani A, Al Maki N, Al Hashmi N.
Al Balushi A, et al. Among authors: al maimani a.
J Pediatr Genet. 2023 Feb 24;13(3):175-180. doi: 10.1055/s-0043-1764127. eCollection 2024 Sep.
J Pediatr Genet. 2023.
PMID: 39086452
Free PMC article.
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Spondylo-ocular Syndrome Due to a Novel Variant in XYLT2 in an Omani Patient.
Al-Araimi M, Hamza N, Al-Hosni A, Al Maimani A.
Al-Araimi M, et al. Among authors: al maimani a.
J Pediatr Genet. 2020 Jul 29;11(1):59-62. doi: 10.1055/s-0040-1715113. eCollection 2022 Mar.
J Pediatr Genet. 2020.
PMID: 35186392
Free PMC article.
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