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Molecular Basis of ...
Molecular Basis of Primary Hyperparathyroidism
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- Björklund, Peyman (författare)
- Uppsala universitet,Endokrinkirurgi
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- Starker, Lee F (författare)
- Department of Surgery, Yale University School of Medicine, New Haven, CT, USA
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Fonseca, A (författare)
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Carling, T (författare)
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(creator_code:org_t)
- 2010
- 2010
- Engelska.
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Ingår i: World Journal of Endocrine Surgery. - 0975-5039. ; 2:2, s. 63-70
- Relaterad länk:
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https://urn.kb.se/re...
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Abstract
Ämnesord
Stäng
- During the past decade and a half, studies of genetic predisposition, parathyroid tumorigenesis, and molecular genetics of familialhyperparathyroid disorders have started to unveil the molecular basis of pHPT. Primary HPT is found in several distinct disorders withautosomal dominant inheritance such as in multiple endocrine neoplasia type 1 (MEN1), MEN2A, the HPT-jaw tumor syndrome (HPT-JT),familial isolated hyperparathyroidism (FIHPT), autosomal dominant mild hyperparathyroidism (ADMH), and neonatal severe HPT (NSHPT).
Nyckelord
- Primary hyperparathyroidism
- familial
- multiglandular
Publikations- och innehållstyp
- vet (ämneskategori)
- art (ämneskategori)
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