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Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population.
Mol Cell Endocrinol. 2018 Feb 5;461:105-111. doi: 10.1016/j.mce.2017.08.022. Epub 2017 Sep 6.
Mol Cell Endocrinol. 2018.
PMID: 28870780
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: alhomaidah ds.
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
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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.
Thyroid. 2016 Feb;26(2):235-41. doi: 10.1089/thy.2015.0510. Epub 2016 Jan 21.
Thyroid. 2016.
PMID: 26711586
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Coexistence of endocrinopathies in children with rheumatic diseases.
Alhomaidah D, Alsagheir A, Al-Mayouf SM.
Alhomaidah D, et al.
Int J Pediatr Adolesc Med. 2016 Sep;3(3):119-122. doi: 10.1016/j.ijpam.2016.04.002. Epub 2016 May 24.
Int J Pediatr Adolesc Med. 2016.
PMID: 30805481
Free PMC article.
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