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5. Congenital familial hypoparathyroidism. Management of an infant, genetics, pathogenesis of hypoparathyroidism, and fetal undermineralization. Gorodischer R; Aceto T; Terplan K Am J Dis Child; 1970 Jan; 119(1):74-8. PubMed ID: 5308088 [No Abstract] [Full Text] [Related]
6. Familial hypoparathyroidism: identification of a novel gain of function mutation in transmembrane domain 5 of the calcium-sensing receptor. Watanabe T; Bai M; Lane CR; Matsumoto S; Minamitani K; Minagawa M; Niimi H; Brown EM; Yasuda T J Clin Endocrinol Metab; 1998 Jul; 83(7):2497-502. PubMed ID: 9661634 [TBL] [Abstract][Full Text] [Related]
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8. Familial isolated hypoparathyroidism: case report with serum PTHrP examination. Koshiyama H; Mori S; Koh T; Tatsuoka Y; Mune T; Katakami H Endocr J; 1996 Oct; 43(5):569-72. PubMed ID: 8980898 [TBL] [Abstract][Full Text] [Related]
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12. Activating mutations of the calcium-sensing receptor: management of hypocalcemia. Lienhardt A; Bai M; Lagarde JP; Rigaud M; Zhang Z; Jiang Y; Kottler ML; Brown EM; Garabédian M J Clin Endocrinol Metab; 2001 Nov; 86(11):5313-23. PubMed ID: 11701698 [TBL] [Abstract][Full Text] [Related]
13. Familial early hypoparathyroidism associated with hypomagnesaemia. Niklasson E Acta Paediatr Scand; 1970 Nov; 59(6):715-9. PubMed ID: 5312271 [No Abstract] [Full Text] [Related]
14. [Vitamin D3 in the combined treatment of patient with hypoparathyroidism]. Komissarenko IV; Pomerantsev IuV; Zavernyĭ IuL Vrach Delo; 1989 Jul; (7):14-6. PubMed ID: 2552680 [TBL] [Abstract][Full Text] [Related]
15. Autosomal dominant hypoparathyroidism with intracranial calcification outside the basal ganglia. McLeod DR; Hanley DA; McArthur RG Am J Med Genet; 1989 Jan; 32(1):32-5. PubMed ID: 2705481 [TBL] [Abstract][Full Text] [Related]
16. A familial syndrome of hypocalcemia with hypercalciuria due to mutations in the calcium-sensing receptor. Pearce SH; Williamson C; Kifor O; Bai M; Coulthard MG; Davies M; Lewis-Barned N; McCredie D; Powell H; Kendall-Taylor P; Brown EM; Thakker RV N Engl J Med; 1996 Oct; 335(15):1115-22. PubMed ID: 8813042 [TBL] [Abstract][Full Text] [Related]