Erysipelas
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Last Posted: Mar 15, 2023
- Disease severity and genotype-phenotype correlation in adult patients with familial Mediterranean fever.
Tuncer Kuru Fatma, et al. Modern rheumatology 2023 0 - Familial Mediterranean fever in Chinese adult patients.
Wu Di, et al. Rheumatology (Oxford, England) 2018 0 (12) 2140-2144 - Influence of swine leukocyte antigen haplotype on serum antibody titers against swine erysipelas vaccine and reproductive and meat production traits of SLA-defined selectively bred Duroc pigs.
Imaeda Noriaki, et al. The Journal of veterinary medical science 2018 0 (11) 1662-1668 - Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia.
Yildirim Malik Ejder, et al. Annals of Saudi medicine 2019 0 (6) 382-387 - Erysipelas-like erythema in children with familial Mediterranean fever.
Gezgin Yildirim Deniz, et al. Clinical and experimental rheumatology 2020 0 (5) 101-104 - Age of onset as an influencing factor for disease severity in children with familial Mediterranean fever.
Tanatar Ay?e, et al. Modern rheumatology 2020 0 (1) 219-222 - The analysis of genotype-phenotype correlation in familial Mediterranean fever.
Ozturk Kubra, et al. Pediatrics international : official journal of the Japan Pediatric Society 2021 0 (1) e15017 - Presentation of a new mutation in FMF and evaluating the frequency of distribution of the MEFV gene mutation in our region with clinical findings.
Arpac? Abdullah, et al. Molecular biology reports 2021 0 (3) 2025-2033 - Polymorphisms in some proinflammatory genes (TNF? and ?, IL-1?, IL-6, ADAM17) in severe chronic venous disease.
Slonková Veronika, et al. Journal of the European Academy of Dermatology and Venereology : JEADV 2022 0 (3) 590-597 - R202Q prevalence in clinically diagnosed Familial Mediterranean Fever patients: 9 years of data analysis from 1570 patients living Central Black Sea region, Turkey.
Çapraz Mustafa, et al. Irish journal of medical science 2022 0
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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
- Page last updated:Apr 25, 2024
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