Primär hyperparatyreoidism vanligt hos postmenopausala kvinnor. Identifiering av genetiska riskfaktorer kan ge individanpassad behandling
(2001) In Lakartidningen 98(18). p.200-2198- Abstract
Primary hyperparathyroidism (pHPT) is commonly seen in postmenopausal women. Along with the clinical characterisation of the disease, studies of molecular genetics have contributed to increased understanding of the etiology of pHPT. Genetic association studies have revealed that certain vitamin D receptor polymorphisms relate to the development of sporadic pHPT. A new type of familial pHPT was recently discovered. Studies of parathyroid adenomas have demonstrated that the tumor suppressor gene MEN1 and the oncogene cyclinD1 are of importance for the tumorigenesis.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/ae4b20db-4cc5-4714-9819-06e7616577d0
- author
- Correa, Pamela LU ; Szabo, Eva ; Lundgren, Ewa and Carling, Tobias
- alternative title
- Primary hyperparathyroidism is common among postmenopausal women. Identification of genetic risk factors can contribute to individualized treatment
- publishing date
- 2001
- type
- Contribution to specialist publication or newspaper
- publication status
- published
- keywords
- Aged, Calcium/metabolism, Female, Genes, bcl-1, Genetic Predisposition to Disease, Humans, Hyperparathyroidism/diagnosis, Middle Aged, Parathyroid Hormone/genetics, Postmenopause, Risk Factors
- in
- Lakartidningen
- volume
- 98
- issue
- 18
- pages
- 200 - 2198
- publisher
- Swedish Medical Association
- external identifiers
-
- pmid:11402599
- scopus:0035795832
- ISSN
- 0023-7205
- language
- Swedish
- LU publication?
- no
- id
- ae4b20db-4cc5-4714-9819-06e7616577d0
- alternative location
- https://lakartidningen.se/wp-content/uploads/OldPdfFiles/2001/22869.pdf
- date added to LUP
- 2021-12-29 12:27:18
- date last changed
- 2024-01-05 23:28:08
@misc{ae4b20db-4cc5-4714-9819-06e7616577d0, abstract = {{<p>Primary hyperparathyroidism (pHPT) is commonly seen in postmenopausal women. Along with the clinical characterisation of the disease, studies of molecular genetics have contributed to increased understanding of the etiology of pHPT. Genetic association studies have revealed that certain vitamin D receptor polymorphisms relate to the development of sporadic pHPT. A new type of familial pHPT was recently discovered. Studies of parathyroid adenomas have demonstrated that the tumor suppressor gene MEN1 and the oncogene cyclinD1 are of importance for the tumorigenesis.</p>}}, author = {{Correa, Pamela and Szabo, Eva and Lundgren, Ewa and Carling, Tobias}}, issn = {{0023-7205}}, keywords = {{Aged; Calcium/metabolism; Female; Genes, bcl-1; Genetic Predisposition to Disease; Humans; Hyperparathyroidism/diagnosis; Middle Aged; Parathyroid Hormone/genetics; Postmenopause; Risk Factors}}, language = {{swe}}, number = {{18}}, pages = {{200--2198}}, publisher = {{Swedish Medical Association}}, series = {{Lakartidningen}}, title = {{Primär hyperparatyreoidism vanligt hos postmenopausala kvinnor. Identifiering av genetiska riskfaktorer kan ge individanpassad behandling}}, url = {{https://lakartidningen.se/wp-content/uploads/OldPdfFiles/2001/22869.pdf}}, volume = {{98}}, year = {{2001}}, }