Optic Neuritis
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Last Posted: Aug 15, 2024
- HLA-DR genotypes in patients with primary Sjögren's syndrome in Taiwan.
Chang-Yi Yen, et al. The Kaohsiung journal of medical sciences 2024 0 - Association of interleukin-17F (rs763780) single nucleotide polymorphism with multiple sclerosis and optic neuritis.
Shereen Salah, et al. Scientific reports 2024 0 (1) 13643 - Investigating the Relationship between Telomere-Related Gene Variants and Leukocyte Telomere Length in Optic Neuritis Patients.
Monika Duseikaite, et al. Journal of clinical medicine 2024 0 (9) - Optic Neuritis: The Influence of Gene Polymorphisms and Serum Levels of STAT4 (rs10181656, rs7574865, rs7601754, rs10168266).
Greta Gedvilaite, et al. Journal of clinical medicine 2024 0 (1) - Association of retinal vessel pathology and brain atrophy in relapsing-remitting multiple sclerosis.
Eva Feodora Romahn, et al. Frontiers in immunology 2023 0 1284986 - The role of SIRT1 level and SIRT1 gene polymorphisms in optic neuritis patients with multiple sclerosis.
Kubiliute Aleksandra, et al. Orphanet journal of rare diseases 2023 0 (1) 64 - Mendelian randomization analysis reveals causal relationships between gut microbiome and optic neuritis.
Liu Kangcheng, et al. Human genetics 2022 0 - A prospective case-control study comparing optical coherence tomography characteristics in neuromyelitis optica spectrum disorder- optic neuritis and idiopathic optic neuritis.
Zhao Xiujuan, et al. BMC ophthalmology 2018 0 (1) 247 - Association of MMP-2 (?1306 C/T) Gene Polymorphism with Predisposition to Optic Neuritis and Optic Neuritis Together with Multiple Sclerosis.
Liutkevi?ien? Rasa, et al. Medicina (Kaunas, Lithuania) 2018 0 (2) - Does CETP rs5882, rs708272, SIRT1 rs12778366, FGFR2 rs2981582, STAT3 rs744166, VEGFA rs833068, IL6 rs1800795 polymorphisms play a role in optic neuritis development?
Gedvilaite Greta, et al. Ophthalmic genetics 2019 0 (3) 219-226
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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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