Uncertainties in distinction of typical primary hyperparathyroidism from familial hypocalciuric hypercalcemia.
作者信息
Marx S J
出版信息
West J Med. 1982 Feb;136(2):145-5.
Abstract
摘要
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本文引用的文献
1
Familial hypocalciuric hypercalcemia: recognition among patients referred after unsuccessful parathyroid exploration.家族性低钙血症性高钙血症：在甲状旁腺探查失败后转诊患者中的识别。
Ann Intern Med. 1980 Mar;92(3):351-6. doi: 10.7326/0003-4819-92-3-351.
2
Primary hyperparathyroidism. Incidence, morbidity, and potential economic impact in a community.原发性甲状旁腺功能亢进症。社区中的发病率、患病率及潜在经济影响。
N Engl J Med. 1980 Jan 24;302(4):189-93. doi: 10.1056/NEJM198001243020402.
3
The hypocalciuric or benign variant of familial hypercalcemia: clinical and biochemical features in fifteen kindreds.家族性高钙血症的低钙尿症或良性变异型：15个家系的临床和生化特征
Medicine (Baltimore). 1981 Nov;60(6):397-412. doi: 10.1097/00005792-198111000-00002.
4
The parathyroid glands in familial hypocalciuric hypercalcemia.家族性低钙血症性高钙血症中的甲状旁腺
Hum Pathol. 1981 Mar;12(3):229-37. doi: 10.1016/s0046-8177(81)80123-2.
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Combined treatment with sustained-release theophylline and beta2-adrenoceptor-stimulating agents in chronic childhood asthma.长效茶碱与β2 - 肾上腺素受体激动剂联合治疗儿童慢性哮喘。
Br Med J (Clin Res Ed). 1981 Mar 28;282(6269):1029-31. doi: 10.1136/bmj.282.6269.1029.
6
Maximal urine-concentrating ability: familial hypocalciuric hypercalcemia versus typical primary hyperparathyroidism.最大尿浓缩能力：家族性低钙血症性高钙血症与典型原发性甲状旁腺功能亢进症的比较
J Clin Endocrinol Metab. 1981 Apr;52(4):736-40. doi: 10.1210/jcem-52-4-736.
7
Primary hyperparathyroidism: changes in the pattern of clinical presentation.原发性甲状旁腺功能亢进症：临床表现模式的变化
Lancet. 1980 Jun 21;1(8182):1317-20. doi: 10.1016/s0140-6736(80)91783-3.
8
Familial benign hypercalcemia.家族性良性高钙血症
J Pediatr. 1972 Dec;81(6):1060-7. doi: 10.1016/s0022-3476(72)80232-4.
9
Family studies in patients with primary parathyroid hyperplasia.原发性甲状旁腺增生患者的家族研究。
Am J Med. 1977 May;62(5):698-706. doi: 10.1016/0002-9343(77)90873-7.
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Neonatal primary hyperparathyroidism with autosomal dominant inheritance.具有常染色体显性遗传的新生儿原发性甲状旁腺功能亢进症。
J Pediatr. 1977 Feb;90(2):269-72. doi: 10.1016/s0022-3476(77)80649-5.
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