Haemophilus Influenzae
What's New
Last Posted: Jan 24, 2024
- Gene polymorphisms of IL-17A and bacterial meningitis in Angolan children.
Johanna Teräsjärvi, et al. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2024 0 105553 - Bacterial Etiology in Subacute Cough.
Ji-Yong Moon, et al. Allergy, asthma & immunology research 2023 0 - Antecedent infections, recent developments and future directions in Guillain-Barré syndrome.
Iqbal Rashid, et al. JPMA. The Journal of the Pakistan Medical Association 2023 0 (1) 117-124 - Genetic mannose binding lectin deficiency is associated with airway microbiota diversity and reduced exacerbation frequency in COPD.
Dicker Alison J, et al. Thorax 2017 0 (6) 510-518 - Differential distribution of IgA-protease genotypes in mucosal and invasive isolates of Haemophilus influenzae in Sweden.
Resman Fredrik, et al. BMC infectious diseases 2018 0 (1) 592 - FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Santos-Cortez Regie Lyn P, et al. American journal of human genetics 2018 0 (5) 679-690 - Gene Polymorphisms of TLR4 and TLR9 and Haemophilus influenzae Meningitis in Angolan Children.
Tenhu Elina, et al. Genes 2020 0 (9) - Detection of Cell-Dissociated Non-Typeable Haemophilus influenzae in the Airways of Patients with Chronic Obstructive Pulmonary Disease.
Thulborn Samantha J, et al. International journal of chronic obstructive pulmonary disease 2020 0 1357-1365 - Genetic predisposition to adverse events in Chinese children aged 3-24 months after diphtheria, tetanus, acellular pertussis and haemophilus influenzae type b combined vaccination.
Ma Yujia, et al. Expert review of vaccines 2022 0 (12) 1923-1928 - Similar humoral immunity parameters in chronic lymphocytic leukemia patients independent of VH gene mutation status.
Sinisalo Marjatta, et al. Leukemia & lymphoma 2004 0 (12) 2451-4
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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
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