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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. 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.
Spectrum of the KIT Gene Mutations in Gastrointestinal Stromal Tumors in Arab Patients.
Faiyaz-Ul-Haque M, Al-Dayel F, Tulba A, Abalkhail H, Alhussaini H, Memon M, Bazarbashi S, Amin T, Satti MB, Peltekova I, Nawaz Z, Zaidi SH. Faiyaz-Ul-Haque M, et al. Asian Pac J Cancer Prev. 2018 Oct 26;19(10):2905-2910. doi: 10.22034/APJCP.2018.19.10.2905. Asian Pac J Cancer Prev. 2018. PMID: 30362320 Free PMC article.
52 results