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The spectrum of the hypoparathyroid states: A classification based on physiologic principles.

作者信息

Nusynowitz M L, Frame B, Kolb F O

出版信息

Medicine (Baltimore). 1976 Mar;55(2):105-19. doi: 10.1097/00005792-197603000-00001.

DOI:10.1097/00005792-197603000-00001
PMID:768709
Abstract
摘要

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Multiple brown tumors: a bone complication due to long-term untreated pseudohypoparathyroidism.多发性棕色瘤：由于长期未治疗的假性甲状旁腺功能减退症引起的骨骼并发症。
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Pseudohypoparathyroidism presenting as renal osteodystrophy.
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Deficient guanine nucleotide regulatory unit activity in cultured fibroblast membranes from patients with pseudohypoparathyroidism type I. a cause of impaired synthesis of 3',5'-cyclic AMP by intact and broken cells.I型假性甲状旁腺功能减退症患者培养的成纤维细胞膜中鸟嘌呤核苷酸调节单位活性不足。完整细胞和破碎细胞合成3',5'-环磷酸腺苷受损的一个原因。
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J Med Genet. 1981 Dec;18(6):431-5. doi: 10.1136/jmg.18.6.431.
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Secondary hyperparathyroidism with 1,25-dihydroxyvitamin D deficiency and pseudohypoparathyroidism in childhood: relationship between plasma 1,25-dihydroxyvitamin D and parathyroid hormone levels and urinary cyclic AMP response to exogenous PTH.儿童继发性甲状旁腺功能亢进伴1,25 - 二羟维生素D缺乏及假性甲状旁腺功能减退：血浆1,25 - 二羟维生素D与甲状旁腺激素水平及尿中环磷酸腺苷对外源性甲状旁腺激素反应之间的关系
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Primary familial hypoparathyroidism with an autosomal dominant mode of inheritance.
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