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Fukumoto S, Namba N, Ozono K, et al. Causes and differential diagnosis of hypocalcemia-recommendation proposed by expert panel supported by Ministry of Health, Labour and Welfare, Japan. Endocr J 55: 787-794, 2008.","DOI":"10.1507\/endocrj.K08E-076"},{"key":"2","unstructured":"2. Lienhardt A, Bai M, Lagarde JP, et al. Activating mutations of the calcium-sensing receptor: management of hypocalcemia. J Clin Endocrinol Metab 86: 5313-5323, 2001."},{"key":"3","unstructured":"3. Gunn IR, Gaffney D. Clinical and laboratory features of calcium-sensing receptor disorders: a systematic review. Ann Clin Biochem 41: 441-458, 2004."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Pllak MR, Brown EM, Estep HL, et al. Autosomal dominant hypocalcemia caused by a Ca<sup>2+<\/sup>-sensing receptor gene mutation. Nat Genet 8: 303-307, 1994.","DOI":"10.1038\/ng1194-303"},{"key":"5","unstructured":"5. Mittelman SD, Hendy GN, Fefferman RA, et al. A hypocalcemic child with a novel activating mutation of the calcium-sensing receptor gene: successful treatment with recombinant human parathyroid hormone. J Clin Endocrinol Metab 91: 2474-2479, 2006."},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Canaff L, Hendy GN. Human calcium-sensing receptor gene. Vitamin D response elements in promoters P1 and P2 confer transcriptional responsiveness to 1,25-dihydroxyvitamin D. J Biol Chem 277: 30337-30350, 2002.","DOI":"10.1074\/jbc.M201804200"},{"key":"7","unstructured":"7. Heihachirou A, Seihou K. Parathyroid disease, Nerve and muscular symptom. Neurology 21: 199-215, 1984."},{"key":"8","doi-asserted-by":"crossref","unstructured":"8. Chou YH, Brown EM, Levi T, et al. The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families. Nat Genet 1: 295-300, 1997.","DOI":"10.1038\/ng0792-295"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Baron J, Winer KK, Yanovski JA, et al. Mutations in the Ca<sup>2+<\/sup>-sensing receptor gene cause autosomal dominant and sporadic hypoparathyroidism. Hum Mol Genet 5: 601-606, 1996.","DOI":"10.1093\/hmg\/5.5.601"},{"key":"10","unstructured":"10. Pidasheva S, D'Souza-Li L, Canaff L, Cole DE, Hendy GN. CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia. Hum Mutat 24: 107-111, 2004."},{"key":"11","doi-asserted-by":"crossref","unstructured":"11. Hirai H, Nakajima S, Miyaguchi A, et al. A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia. J Hum Genet 46: 41-44, 2001.","DOI":"10.1007\/s100380170124"},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Brannan TS, Burger AA, Chaudhary MY. Bilateral basal ganglia calcifications visualized on CT scan. J Neurol Neurosurg Psychiatry 43: 403-406, 1980.","DOI":"10.1136\/jnnp.43.5.403"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Illum F, Dupont E. Prevalences of CT-detected calcification in the basal ganglia in idiopathic hypoparathyroidism and pseudohypoparathyroidism. Neuroradiology 27: 32-37, 1985.","DOI":"10.1007\/BF00342514"},{"key":"14","unstructured":"14. Raue F, Pichl J, Dorr HG, et al. Activating mutations in the calcium sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcemia-a German survey. Clin Endocrinol 75: 760-765, 2011."},{"key":"15","unstructured":"15. Smits M, Gabreels F, Froeling P, et al. Autosomal dominant idiopathic hypoparathyroidism and nervous system dysfunction: report of three cases and review of the literature. J Neurol 228: 113-122, 1982."},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Abe S, Tojo K, Shigematsu T, Hasegawa T, Morita M, Sakai O. A rare case of idiopathic hypoparathyroidism with varied neurological manifestations. Intern Med 35: 129-134, 1996.","DOI":"10.2169\/internalmedicine.35.129"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17. Goel A, Bhatnagar MK, Vashishta A, Verma NP. Hypoparathyroidism with extensive intracranial calcification. Postgrad Med J 70: 913-915, 1994.","DOI":"10.1136\/pgmj.70.830.913"},{"key":"18","doi-asserted-by":"crossref","unstructured":"18. Boller F, Boller N, Gilbert J. Familial idiopathic cerebral calcification. J Neurol Neurosurg Psychiatry 40: 280-285, 1977.","DOI":"10.1136\/jnnp.40.3.280"},{"key":"19","doi-asserted-by":"crossref","unstructured":"19. McKinney AS. Idiopathic hypoparathyroidism presenting as chorea. Neurology 12: 485-491, 1962.","DOI":"10.1212\/WNL.12.7.485"},{"key":"20","doi-asserted-by":"crossref","unstructured":"20. Muenter MD, Whisnant JP. Basal ganglia calcification, hypoparathyroidism and extrapyramidal motor manifestations. 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