Restless Legs Syndrome
What's New
Last Posted: Apr 24, 2024
- Patients with restless legs syndrome exhibit reduced serum colony-stimulating factor-1, humanin-like 3 and 10 levels.
Asena Gülçiçek, et al. Acta neurologica Belgica 2024 0 - Genetic Association Studies in Restless Legs Syndrome: Risk variants & Ethnic differences.
Brendan Jen-Wei Tan, et al. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2024 0 1-31 - Genomic analysis identifies risk factors in restless legs syndrome.
Fulya Akçimen, et al. medRxiv : the preprint server for health sciences 2024 0 - Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutations.
De Michele Giovanna, et al. Acta neurologica Belgica 2023 0 (1) 221-226 - A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1.
Catoire Helene, et al. Scientific reports 2018 0 (1) 12173 - Systematic review and meta-analysis of observational studies to understand the prevalence of restless legs syndrome in multiple sclerosis: an update.
Ning Pingping, et al. Sleep medicine 2018 0 97-104 - Assessment of cardiac autonomic functions by heart rate variability in patients with restless leg syndrome.
Y?ld?z Abdülmelik, et al. Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2018 0 (3) 191-196 - Genetic Variations Associated with Sleep Disorders in Patients with Schizophrenia: A Systematic Review.
Assimakopoulos Konstantinos, et al. Medicines (Basel, Switzerland) 2018 0 (2) - Prognostic Impact of Restless Legs Syndrome on Patients with Heart Failure.
Yoshihisa Akiomi, et al. International heart journal 2019 0 (5) 1098-1105 - Study on sleep-wake disorders in patients with genetic and non-genetic amyotrophic lateral sclerosis.
Sun Xiaohan, et al. Journal of neurology, neurosurgery, and psychiatry 2020 0 - Difference in background factors between responders to gabapentin enacarbil treatment and responders to placebo: pooled analyses of two randomized, double-blind, placebo-controlled studies in Japanese patients with restless legs syndrome.
Inoue Yuichi, et al. Sleep medicine 2021 0 138-146 - Association of BST1 polymorphism with idiopathic restless legs syndrome in Chinese population.
Huang Yumeng, et al. Sleep & breathing = Schlaf & Atmung 2021 0 (4) 1987-1993 - Correction to: Serum vitamin D, vitamin D receptor and binding protein genes polymorphisms in restless legs syndrome.
Jiménez-Jiménez Félix Javier, et al. Journal of neurology 2021 0 (4) 1473 - LAG3/CD4 Genes Variants and the Risk for Restless Legs Syndrome.
Jiménez-Jiménez Félix Javier, et al. International journal of molecular sciences 2022 0 (23) - The frequency of non-motor symptoms in SCA3 and their association with disease severity and lifestyle factors.
Hengel Holger, et al. Journal of neurology 2022 0 (2) 944-952 - ExomeChip-based rare variant association study in restless legs syndrome.
Tilch Erik, et al. Sleep medicine 2022 0 26-30 - Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs.
Jiang Yun-Jin, et al. The journal of headache and pain 2022 0 (1) 39 - Pleiotropic genetic effects influencing sleep and neurological disorders.
Veatch Olivia J, et al. The Lancet. Neurology 2017 0 (2) 158-170 - Screening of novel restless legs syndrome-associated genes in French-Canadian families.
Akçimen Fulya, et al. Neurology. Genetics 2019 0 (6) e296 - Genetic heterogeneity on sleep disorders in Parkinson's disease: a systematic review and meta-analysis.
Huang Jingxuan et al. Translational neurodegeneration 2022 11(1) 21
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HLBS-PopOmics is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other materials that address the translation of genomic and other precision health discoveries into improved health care and prevention related to Heart and Vascular Diseases(H), Lung Diseases(L), Blood Diseases(B), and Sleep Disorders(S)...more
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Mensah GA, Yu W, Barfield WL, Clyne M, Engelgau MM, Khoury MJ. HLBS-PopOmics: an online knowledge base to accelerate dissemination and implementation of research advances in population genomics to reduce the burden of heart, lung, blood, and sleep disorders. Genet Med. 2018 Sep 10. doi: 10.1038/s41436-018-0118-1
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
- Page last updated:May 18, 2024
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