Similar articles

• Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion.

  Christenson RA, Pootrakul P, Burnell JM, Teubner EJ, Finch CA, Baylink DJ. Christenson RA, et al. Birth Defects Orig Artic Ser. 1987;23(5A):409-16. Birth Defects Orig Artic Ser. 1987. PMID: 3689925 No abstract available.
• Under-recognized Hypoparathyroidism in Thalassemia.

  Tangngam H, Mahachoklertwattana P, Poomthavorn P, Chuansumrit A, Sirachainan N, Chailurkit L, Khlairit P. Tangngam H, et al. J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):324-330. doi: 10.4274/jcrpe.0020. Epub 2018 May 4. J Clin Res Pediatr Endocrinol. 2018. PMID: 29726397 Free PMC article.
• The spectrum of parathyroid function in thalassaemia subjects with transfusional iron overload.

  Brezis M, Shalev O, Leibel B, Dagan I, Ben-Ishay D. Brezis M, et al. Miner Electrolyte Metab. 1982 Dec;8(6):307-13. Miner Electrolyte Metab. 1982. PMID: 6300636 No abstract available.
• A case of hypoparathyroidism in a child with beta-thalassemia successfully treated with 1 alpha-hydroxy-vitamin D3.

  Matsaniotis N, Karpathios T, Nicolaidou P, Bacopoulos C, Thomaidis T. Matsaniotis N, et al. Helv Paediatr Acta. 1981;36(2):171-3. Helv Paediatr Acta. 1981. PMID: 7251388
• Is there a standard-of-care for transfusion therapy in thalassemia?

  Franchini M, Forni GL, Liumbruno GM. Franchini M, et al. Curr Opin Hematol. 2017 Nov;24(6):558-564. doi: 10.1097/MOH.0000000000000373. Curr Opin Hematol. 2017. PMID: 28719386 Review.