Familial Mediterranean Fever
Last Posted: Nov 04, 2021
- The Assessment of Selected miRNA Profile in Familial Mediterranean Fever.
Kahraman Cigdem Yuce et al. BioMed research international 2021 20216495700
- The analysis of genotype-phenotype correlation in familial Mediterranean fever.
Öztürk Kübra et al. Pediatrics international : official journal of the Japan Pediatric Society 2021
- Non-adherence to colchicine treatment is a common misevaluation in familial Mediterranean fever.
Tekgöz Emre et al. Turkish journal of medical sciences 2021
- COVID-19 outcomes in patients with familial Mediterranean fever: a retrospective cohort study.
Güven Serdar Can et al. Rheumatology international 2021
- Clinical significance of E148Q heterozygous variant in paediatric Familial Mediterranean Fever.
Tirosh Irit et al. Rheumatology (Oxford, England) 2021 Feb
- Chronic non-bacterial osteomyelitis: another disease associated with MEFV gene mutations.
Avar-Aydin Pinar Ozge et al. Clinical and experimental rheumatology 2020 Nov
- Comparison of the clinical diagnostic criteria and the results of the next-generation sequence gene panel in patients with monogenic systemic autoinflammatory diseases.
Sözeri Betül et al. Clinical rheumatology 2020 Nov
- Clinical course of COVID-19 in a cohort of 342 familial Mediterranean fever patients with a long-term treatment by colchicine in a French endemic area.
Bourguiba Rim et al. Annals of the rheumatic diseases 2020 Nov
- Erysipelas-like erythema in children with familial Mediterranean fever.
Gezgin Yildirim Deniz et al. Clinical and experimental rheumatology 2020 Oct
- Familial Mediterranean Fever: Clinical State Of The Art.
Egeli Bugra Han et al. QJM : monthly journal of the Association of Physicians 2020 Oct
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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