Last Posted: Mar 06, 2023
- Genes and their single nucleotide polymorphism involved in innate immune response in central nervous system in bacterial meningitis: review of literature data.
Gowin Ewelina, et al. Inflammation research : official journal of the European Histamine Research Society ... [et al.] 2018 0 (8) 655-661
- Clinical presentations, Laboratory analysis and Linear Growth in 50 Neonates and Young Infants with Acute Meningitis: One Year Experience of a Single Center in Qatar.
Abdelmaguid Nadra, et al. Mediterranean journal of hematology and infectious diseases 2019 0 (1) e2019028
- Gene Polymorphisms of TLR4 and TLR9 and Haemophilus influenzae Meningitis in Angolan Children.
Tenhu Elina, et al. Genes 2020 0 (9)
- TLR9 Rs352140 polymorphism contributes to a decreased risk of bacterial meningitis: evidence from a meta-analysis.
Xue Haiyi, et al. Epidemiology and infection 2020 0 e294
- Complement factor H contributes to mortality in humans and mice with bacterial meningitis.
Kasanmoentalib E Soemirien, et al. Journal of neuroinflammation 2019 0 (1) 279
- Individual responsiveness of macrophage migration inhibitory factor predicts long-term cognitive impairment after bacterial meningitis.
Kloek Anne T, et al. Acta neuropathologica communications 2021 0 (1) 4
- Study protocol: The Dutch 20|30 Postmeningitis study: a cross-sectional follow-up of two historical childhood bacterial meningitis cohorts on long-term outcomes.
El Tahir O, et al. BMC pediatrics 2020 0 (1) 519
- Derivation of a clinical-based model to detect invasive bacterial infections in febrile infants.
Yaeger Jeffrey P et al. Journal of hospital medicine 2022
- Gene polymorphisms of TLR10: effects on bacterial meningitis outcomes in Angolan children.
Tenhu Elina, et al. APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 2022 2
- Ability of Procalcitonin and C-Reactive Protein for Discriminating between Bacterial and Enteroviral Meningitis in Children Using Decision Tree.
Babenko Dmitriy et al. BioMed research international 2021 20215519436
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
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Graves Disease
- Huntington Disease
- Myasthenia Gravis
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics 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, 2023
- Page last updated:Jun 09, 2023
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