Transverse Myelitis
What's New
Last Posted: May 01, 2023
- What Kept Back on the Mirror of COVID-19-Related Acute Transverse Myelitis? A Genetic Background!
Reza Sinaei, et al. Iranian journal of child neurology 2023 0 (2) 143-147 - Familial monophasic acute transverse myelitis due to the pathogenic variant in VPS37A.
Mealy Maureen A, et al. Neurology. Genetics 2018 0 (1) e213 - Genetic factors for susceptibility to and manifestations of neuromyelitis optica.
Matsushita Takuya, et al. Annals of clinical and translational neurology 2020 0 (11) 2082-2093 - Long-Term Outcome of a Series of Patients With Narcolepsy Type 1 and Comorbidity With Immunopathological and Autoimmune Diseases.
Martinez-Orozco Francisco J, et al. Journal of clinical medicine research 2022 0 (8) 309-314 - Patients with laboratory criteria of anti-phospholipid syndrome and 'non-criteria' manifestations: a multicenter cohort.
Pires da Rosa G, et al. Scandinavian journal of rheumatology 2022 0 (2) 190-195 - A case of refractory systemic lupus erythematosus with monocytosis exhibiting somatic KRAS mutation.
Law Sze-Ming, et al. Inflammation and regeneration 2022 0 (1) 10 - Association of HLA DRB1-DQB1 Haplotypes with the Risk for Neuromyelitis Optica among South Indians.
Kanikannan Meena A, et al. Neurology India 0 0 (4) 1481-1486 - Association between covid-19 vaccination, SARS-CoV-2 infection, and risk of immune mediated neurological events: population based cohort and self-controlled case series analysis.
Li Xintong et al. BMJ (Clinical research ed.) 2022 3 e068373 - [Correlation of AQP4 gene polymorphism with NMO clinical phenotypes and its underlying mechanism].
Qiu Wei, et al. Zhonghua yi xue za zhi 2015 2 (7) 501-6 - Association Between the Single Nucleotide Polymorphism and the Level of Aquaporin-4 Protein Expression in Han and Minority Chinese with Inflammatory Demyelinating Diseases of the Central Nervous System.
Chu Lan, et al. Molecular neurobiology 2015 4
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
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
- Content source: