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Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation.
Faiyaz-Ul-Haque M, AlDhalaan W, AlAshwal A, Bin-Abbas BS, AlSagheir A, Alotaiby M, Rafiq Z, Zaidi SHE. Faiyaz-Ul-Haque M, et al. Among authors: alashwal a. J Pediatr Endocrinol Metab. 2018 Aug 28;31(8):861-868. doi: 10.1515/jpem-2017-0312. J Pediatr Endocrinol Metab. 2018. PMID: 29949513 Free article.
Endocrine sequelae of childhood craniopharyngioma.
Bin-Abbas B, Mawlawi H, Sakati N, Khafaja Y, Chaudhary MA, Al-Ashwal A. Bin-Abbas B, et al. J Pediatr Endocrinol Metab. 2001 Jul-Aug;14(7):869-74. doi: 10.1515/jpem.2001.14.7.869. J Pediatr Endocrinol Metab. 2001. PMID: 11515727
60 results