The need for national registries for rare endocrine tumor syndromes

Endocrine. 2017 Nov;58(2):205-206. doi: 10.1007/s12020-017-1296-3. Epub 2017 Apr 17.

Authors

Rachel S van Leeuwaarde¹, Wouter W de Herder², Gerlof D Valk¹

Affiliations

¹ Department of Endocrine Oncology, University Medical Center Utrecht, Utrecht, The Netherlands.
² Department of Internal Medicine, Erasmus Medical Center, Rotterdam, The Netherlands. w.w.deherder@erasmusmc.nl.

PMID: 28417312
DOI: 10.1007/s12020-017-1296-3

No abstract available

Publication types

Editorial

MeSH terms

Databases, Factual / standards
Databases, Factual / supply & distribution
Endocrine Gland Neoplasms / epidemiology*
Health Services Needs and Demand* / standards
Humans
Multiple Endocrine Neoplasia Type 1 / epidemiology
Rare Diseases / epidemiology*
Registries*
Syndrome
United States