Narcolepsy
What's New
Last Posted: Aug 23, 2024
- Association between human leukocyte antigen class II-DR-DQ and narcolepsy: a case control study.
Andrea Bacelar, et al. Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine 2024 0 - Estimating the prevalence and clinical causality of obstructive sleep apnea in paediatric narcolepsy patients.
Chaofan Geng, et al. Sleep & breathing = Schlaf & Atmung 2024 0 - High-resolution HLA sequencing and hypocretin receptor 2 autoantibodies in narcolepsy type 1 and type 2.
Samia Hamdan, et al. International journal of immunogenetics 2024 0 - Disadvantaged social status contributed to sleep disorders: An observational and genome-wide gene-environment interaction analysis.
Xin Qi, et al. Sleep health 2024 0 - Correlation analysis between HLA-DQA1*0102/DQB1*0602 genotypes and narcolepsy patients in China.
Wanyu Zhao, et al. Frontiers in neurology 2024 0 1379723 - Single cell transcriptomics of cerebrospinal fluid cells from patients with recent-onset narcolepsy.
Alina Huth, et al. Journal of autoimmunity 2024 0 103234 - Association between idiopathic hypersomnia and a genetic variant in the PER3 gene.
Yoan Cherasse, et al. Journal of sleep research 2024 0 e14146 - Narcolepsy and cardiovascular disease: A two-sample Mendelian randomization study.
Yanmin Tao, et al. Sleep medicine 2023 0 6-12 - Natural Selection Signatures in the Hondo and Ryukyu Japanese Subpopulations.
Xiaoxi Liu, et al. Molecular biology and evolution 2023 0 (10) - The immunopathogenesis of narcolepsy type 1.
Roland S Liblau, et al. Nature reviews. Immunology 2023 0
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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
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