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Page 1
A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population.
Alzahrani AS, Alswailem M, Abbas BB, Qasem E, Alsagheir A, Al Shidhani A, Al Sinani A, Al Badi M, Al-Maqbali A, Al Shawi M, Albunyan A, Bin Nafisah A, Shi Y. Alzahrani AS, et al. Among authors: qasem e. J Endocr Soc. 2021 May 17;5(8):bvab095. doi: 10.1210/jendso/bvab095. eCollection 2021 Aug 1. J Endocr Soc. 2021. PMID: 34258491 Free PMC article.
A high rate of novel CYP11B1 mutations in Saudi Arabia.
Alzahrani AS, Alswailem MM, Murugan AK, Alhomaidah DS, Capper CP, Auchus RJ, Qasem E, Alzahrani OS, Al-Sagheir A, Bin-Abbas B. Alzahrani AS, et al. Among authors: qasem e. J Steroid Biochem Mol Biol. 2017 Nov;174:217-224. doi: 10.1016/j.jsbmb.2017.09.018. Epub 2017 Sep 28. J Steroid Biochem Mol Biol. 2017. PMID: 28962970
Uncommon TERT Promoter Mutations in Pediatric Thyroid Cancer.
Alzahrani AS, Qasem E, Murugan AK, Al-Hindi HN, AlKhafaji D, Almohanna M, Xing M, Alhomaidah D, AlSwailem M. Alzahrani AS, et al. Among authors: qasem e. Thyroid. 2016 Feb;26(2):235-41. doi: 10.1089/thy.2015.0510. Epub 2016 Jan 21. Thyroid. 2016. PMID: 26711586
30 results