Genetic alterations in primary and secondary hyperparathyroidism.

SHAN L; NAKAMURA Y; NAKAMURA M; YOKOI T; KAKUDO K

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J-GLOBAL ID：200902172062058517 Reference number：98A0832932

Genetic alterations in primary and secondary hyperparathyroidism.

原発性及び二次性上皮小体機能亢進症における遺伝的変性

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Material：
Volume： 48 Issue： 8 Page： 569-574 Publication year： Aug. 1998
JST Material Number： W0853A ISSN： 1320-5463 Document type： Article
Article type：文献レビュー Country of issue： Australia (AUS) Language： ENGLISH (EN)

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Endocrine diseases

Reference (54)：

ARNOLD, A. Monoclonality of parathyroid tumors in chronic renal failure and in primary parathyroid hyperplasia. J. Clin. Invest. 1995, 95, 2047-2053
GRIMELIUS, L. Parathyroid histopathology. Endocr. Pathol. 1996, 7, 165-171
TAHARA, H. Molecular basis of hyperparathyroidism. J. Bone Miner. Metab. 1997, 15, 173-178
CALENDER, A. Primary hyperparathyroidism : Genetic heterogeneity suggesting different pathogenesis in sporadic and familial forms of parathyroid hyperplasia and tumors. Eur. J. Endocrinol. 1996, 134, 263-266
FARNEBO, F. Differential loss of heterozygosity in familial, sporadic and uremic hyperparathyroidism. Hum. Genet. 1997, 99, 342-349

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