Harnessing Rift Valley fever virus NSs gene for cancer gene therapy
, 2022 One of the greatest challenges in the treatment of cancer is tumor heterogeneity which results in differential responses to chemotherapy and drugs that work through a single pathway.
Scott, TA, Davis, AM, Morris, KV
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Heterozygous MEFV Mutation Leading to Renal Failure: A Case Study
Global Pediatric HealthFamilial Mediterranean fever (FMF) is an autosomal recessive disorder, particularly common in the Mediterranean area. Mutations in the MEVF gene cause it. AA Amyloidosis is the most severe complication of FMF leading to chronic renal failure. We describe
Souhaila El Gazzane MD +8 more
doaj +1 more source
A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean Fever [PDF]
, 2014 Background: Familial Mediterranean Fever (FMF), characterized by recurrent fever and inflammation of serous membranes, is an autosomal recessive disease caused by mutations in the Mediterranean fever (MEFV) gene.
Hasan Dogan +15 more
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Familial Mediterranean Fever: an unusual cause of liver disease
Italian Journal of Pediatrics, 2019 Background Familial Mediterranean Fever is an autoinflammatory disease typically expressed with recurrent attacks of fever, serositis, aphthous stomatitis, rash. Only a few reports describe the association with hepatic involvement.
Maria Cristina Maggio +2 more
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A Case Of Familial Mediterranean Fever Presenting With Protracted Febrile Myalgia Syndrome
, 2008 Familial Mediterranean fever is the most common in the hereditary periodic fever syndromes. The frequency of vasculitis syndromes are high in familial Mediterranean fever population.
Cüneyt Karagöl +3 more
core
Frequency of Familial Mediterranean Fever Gene Mutation in Patients Presenting With Joint Pain and Diagnosed With Acute Rheumatic Fever. [PDF]
Cureus, 2023 Gullu UU +7 more
europepmc +1 more source
Concurrent TNFRSF1A R92Q and pyrin E230K mutations in a child with multiple sclerosis [PDF]
, 2010 We report a 16-year-old female patient with a severe course of multiple sclerosis and concomitant symptoms suggestive of a hereditary autoinflammatory disease.
K Huss +16 more
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The Turkish Journal of Pediatrics, 2013 Tumor necrosis factor receptor-associated periodic syndrome (TRAPS) is an autosomal dominant autoinflammatory disorder caused by mutations in the TNFRSF1A gene encoding the 55-kDa receptor for tumor necrosis factor (TNF)-α.
Aslı Celebi-Tayfur +4 more
doaj
Immunogenic Potential of the Mediterranean Fever Gene in Patients with Coronavirus Disease: A Cross-Sectional Study. [PDF]
Iran J Med Sci, 2023 Salehzadeh F +5 more
europepmc +1 more source
Neurological Manifestations in Familial Mediterranean Fever: a Genotype-Phenotype Correlation Study
Background and Aims: Familial Mediterranean Fever (FMF) is a periodic auto-inflammatory disease with an autosomal recessive hereditary pattern. The aim of this study is to explain the spectrum of possible neurological manifestations and its genotype ...
مرتضایی, مریم +4 more
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