uu.seUppsala University Publications
Change search
ReferencesLink to record
Permanent link

Direct link
Molecular Basis of Primary Hyperparathyroidism
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Endocrine Surgery.
Department of Surgery, Yale University School of Medicine, New Haven, CT, USA.
2010 (English)In: World Journal of Endocrine Surgery, ISSN 0975-5039, Vol. 2, no 2, 63-70 p.Article in journal (Other academic) Published
Abstract [en]

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).

Place, publisher, year, edition, pages
2010. Vol. 2, no 2, 63-70 p.
Keyword [en]
Primary hyperparathyroidism, familial, multiglandular
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-197681OAI: oai:DiVA.org:uu-197681DiVA: diva2:613780
Available from: 2013-04-02 Created: 2013-04-02 Last updated: 2013-04-02Bibliographically approved

Open Access in DiVA

No full text

Other links


Search in DiVA

By author/editor
Björklund, PeymanStarker, Lee F
By organisation
Endocrine Surgery
Medical and Health Sciences

Search outside of DiVA

GoogleGoogle Scholar
The number of downloads is the sum of all downloads of full texts. It may include eg previous versions that are now no longer available

Total: 162 hits
ReferencesLink to record
Permanent link

Direct link