Last Posted: Sep 15, 2019
- Association Between Human Leukocyte Antigen-B*27 and Pathogenesis in Seronegative Spondyloarthropathies in Federation of Bosnia and Herzegovina.
Fejzic Elma, et al. Archives of rheumatology 2019 6 (2) 166-175
- MICA and NKG2D variants as risk factors in spondyloarthritis: a case-control study.
Fechtenbaum Marie, et al. Genes and immunity 2018 9
- Disease-association of different killer cell immunoglobulin-like receptors (KIR) and HLA-C gene combinations in reactive arthritis.
Sun Hong Sheng, et al. Modern rheumatology 2018 5 1-20
- Association of human leukocyte A, B, and DR antigens in Colombian patients with diagnosis of spondyloarthritis.
Santos Ana M, et al. Clinical rheumatology 2016 12
- Attack rate of Chlamydia-induced reactive arthritis and effect of the CCR5-Delta-32 mutation: a prospective analysis.
Carter John D, et al. The Journal of rheumatology 2013 9 (9) 1578-82
- Role of hla-B alleles and clinical presentation of b27 negative spondyloarthritis patients from mumbai, Western India.
Parasannanavar Devaraj J, et al. Autoimmune diseases 2014 0 327315
- The role of monocytes and SLC11A1 polymorphisms in the pathogenesis of Chlamydia-induced reactive arthritis.
Chen YJ, et al. Scandinavian journal of rheumatology 2012 12
- Risk and prognosis of campylobacteriosis in relation to polymorphisms of host inflammatory cytokine genes.
Nielsen H, et al. Scandinavian journal of immunology 2012 4 (4) 449-54
- Reactive arthritis
From NCATS Genetic and Rare Diseases Information Center
- Functional CCR5 receptor protects patients with arthritis from high synovial burden of infecting Chlamydia trachomatis.
Gérard Hervé C, et al. The American journal of the medical sciences 2010 12 (6) 448-51
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
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