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Genetics of parathyroid tumours

Abstract:

Primary hyperparathyroidism (PHPT), due to parathyroid tumours, may occur as part of a complex syndrome or as an isolated (non-syndromic) disorder, and both forms can occur as familial (i.e. hereditary) or non-familial (i.e. sporadic) disease. Syndromic PHPT includes multiple endocrine neoplasia (MEN) types 1 to 4 (MEN1 to MEN4) and the hyperparathyroidism-jaw tumour (HPT-JT) syndrome. Syndromic and hereditary PHPT are often associated with multiple parathyroid tumours, in contrast to spora...

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Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1111/joim.12523

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Institution:
University of Oxford
Division:
MSD
Department:
RDM
Sub department:
OCDEM
Role:
Author
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Funding agency for:
Thakker, R
Grant:
G10001167
More from this funder
Funding agency for:
Thakker, R
Grant:
G10001167
More from this funder
Funding agency for:
Thakker, R
Grant:
G10001167
More from this funder
Funding agency for:
Thakker, R
Grant:
G10001167
More from this funder
Funding agency for:
Thakker, R
Grant:
G10001167
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Publisher:
Wiley Publisher's website
Journal:
Journal of Internal Medicine Journal website
Volume:
280
Issue:
6
Pages:
574–583
Host title:
Journal of Internal Medicine
Publication date:
2016-06-01
Acceptance date:
2017-05-12
DOI:
Source identifiers:
622984
Keywords:
Pubs id:
pubs:622984
UUID:
uuid:bdddf37b-2830-4771-931f-3ab9175d5875
Local pid:
pubs:622984
Deposit date:
2016-05-19

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