Behçet Disease
What's New
Last Posted: Nov 20, 2023
- Association of IL-23R and IL-10 variations with Behçet disease: a genetic analysis study.
Guven Yenmis, et al. Immunologic research 2023 0 - HLA Alleles in a Behçet Disease Multiethnic Population With and Without Ophthalmic Manifestations.
Francisco Assis de Andrade, et al. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases 2023 0 (7) 341-346 - The complex HLA-E-nonapeptide in Behçet disease.
Ángel Luís Castaño-Núñez, et al. Frontiers in immunology 2023 0 1080047 - Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.
Burillo-Sanz Sergio, et al. Scientific reports 2017 0 (1) 8453 - KIR3DL1/S1 Allotypes Contribute Differentially to the Development of Behçet Disease.
Petrushkin Harry, et al. Journal of immunology (Baltimore, Md. : 1950) 2019 0 (6) 1629-1635 - Diverse selection pressures shaping the genetic architecture of behçet disease susceptibility.
Sezgin Efe, et al. Frontiers in genetics 2022 0 983646 - Clinical phenotypes of Korean patients with Behcet disease according to gender, age at onset, and HLA-B51.
Ryu Hee Jung, et al. The Korean journal of internal medicine 2017 0 (5) 1025-1031 - [The etiology, diagnosis, and treatment of neurological complications in Behçet disease and its related disorder Sweet disease].
Hisanaga Kinya, et al. Rinsho shinkeigaku = Clinical neurology 2019 0 (1) 1-12 - Association of single nucleotide polymorphisms in CXCR1, CXCR2 and CXCL5 with Behçet disease: a study in the Denizli province of Turkey.
Ar?kan S, et al. Clinical and experimental dermatology 2021 5 - Tuberculosis Exposure With Risk of Behçet Disease Among Patients With Uveitis.
Zhong Zhenyu, et al. JAMA ophthalmology 2021 2
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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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