HYPERPARATHYROIDISM 3

Known as: HRPT3, FIHP, Hyperparathyroidism, Familial Isolated 
A rare inherited condition in which one or more tumors form in the parathyroid glands (four pea-sized organs found on the thyroid) and cause them to… (More)
National Institutes of Health

Papers overview

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2007
2007
Parafibromin is a tumor suppressor protein encoded by HRPT2, a gene recently implicated in the hereditary hyperparathyroidism-jaw… (More)
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2007
2007
Hypercalcemia in persistent secondary hyperparathyroidism after kidney transplantation is considered to result from increased… (More)
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2006
2006
OBJECTIVE To investigate two patients with the hyperparathyroidism-jaw tumour (HPT-JT) syndrome and three patients with familial… (More)
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2006
2006
UNLABELLED Familial hyperparathyroid syndromes involving mutations of HRPT2 (also CDC73), a tumor suppressor, are important to… (More)
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2006
2006
BACKGROUND A subset of familial isolated primary hyperparathyroidism (FIHP) is a variant of hyperparathyroidism-jaw tumour… (More)
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Highly Cited
2004
Highly Cited
2004
Familial hyperparathyroidism is not uncommon in clinical endocrine practice. It encompasses a spectrum of disorders including… (More)
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2004
2004
BACKGROUND Diagnosing primary hyperparathyroidism (PHP) in patients with osteoporosis is important because of the benefits of… (More)
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Highly Cited
2003
Highly Cited
2003
BACKGROUND Hyperparathyroidism is a common endocrinopathy characterised by the formation of parathyroid tumours. In this study… (More)
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2002
2002
OBJECTIVES Familial hyperparathyroidism may occur as part of hereditary syndromes, including multiple endocrine neoplasia types 1… (More)
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1998
1998
Multiple endocrine neoplasia type 1 (MEN 1) is an autosomal dominant disease characterized by neoplasia of the parathyroid glands… (More)
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