Association between restless legs syndrome and hypertension: a preliminary population-based study in South Tyrol, Italy
✍ Scribed by Giannini, G.; Zanigni, S.; Melotti, R.; Gögele, M.; Provini, F.; Facheris, M. F.; Cortelli, P.; Pramstaller, P. P.
- Book ID
- 120931301
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- English
- Weight
- 468 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1351-5101
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Genetic contributions to restless legs syndrome (RLS) have been consistently recognized from population and family studies. To determine the clinical and genetic features of RLS in a population isolate and explore linkage to three previously described susceptibility loci on chromosomes 12q, 14q, and
## Abstract Three loci for the restless legs syndrome (RLS) on chromosomes 12q, 14q, and 9p (RLS1, RLS2, and RLS3) have been mapped, but no gene has been identified as yet. RLS1 has been confirmed in families from three different populations. We conducted a family‐based association study of 159 Eur
## Abstract Restless legs syndrome (RLS) is a highly prevalent movement disorder. However, prevalences seem to vary amongst different ethnicities. To date, no community‐based prevalence studies on RLS have been reported from the African continent. We have conducted a community‐based, door‐to‐door s
## Abstract ## Objective: We previously mapped a genetic locus for restless legs syndrome (RLS) to chromosome 9p22‐24 (__RLS3__) and a later genome‐wide association study (GWAS) implicated the __PTPRD__ gene at the __RLS3 l__ocus as a susceptibility gene for RLS. However, from the standpoint of ge