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Published in 2022 at "Journal of Clinical Ultrasound"
DOI: 10.1002/jcu.23409
Abstract: The most significant complication in familial mediterranean fever (FMF) patients is dysfunction and organ failure developing depending on amyloid deposition in organs. The golden standard for showing amyloid deposition is the biopsy; however, tissue stiffness…
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Keywords:
fmf patients;
gene mutation;
deposition;
relationship mefv ... See more keywords
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Published in 2020 at "Allergologia et immunopathologia"
DOI: 10.1016/j.aller.2019.12.010
Abstract: BACKGROUND Familial Mediterranean fever (FMF) is the most common auto-inflammatory disease and is characterized by self-limiting episodes of fever and polyserositis. The aim of this study was to determine the atopic clinical findings associated with…
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Keywords:
mefv gene;
mediterranean fever;
familial mediterranean;
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Published in 2022 at "Gene"
DOI: 10.1016/j.gene.2022.146447
Abstract: Familial Mediterranean Fever (FMF, OMIM ID: 249100) is the most common autoinflammatory, autosomal recessive disease caused by mutations in the MEFV gene. It is widespread in the Mediterranean, primarily among Turkish, Armenian, Arab and Jewish.…
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Keywords:
gene allele;
mefv gene;
genotype;
3230 patients ... See more keywords
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Published in 2019 at "Gut"
DOI: 10.1136/gutjnl-2019-319051
Abstract: We read with interest the recent work by Schwerd et al 1 showing yet another example of human monogenic diseases that can present with IBD-like intestinal inflammation. Among the genes and diseases related to these…
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Keywords:
western lowland;
disease;
mefv gene;
case ... See more keywords
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Published in 2019 at "International Journal of Inflammation"
DOI: 10.1155/2019/2578760
Abstract: Background Familial Mediterranean Fever (FMF) is a hereditary autosomal recessive disease which is mainly seen in the Turks, Armenians, Arabs, and Jews. It is characterized by recurrent episodes of fever, polyserositis, and rash. MEFV gene,…
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Keywords:
gene mutations;
mefv gene;
familial mediterranean;
gene ... See more keywords
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Published in 2021 at "Gastroenterology Research and Practice"
DOI: 10.1155/2021/5538150
Abstract: Background The clinical and pathological features of inflammatory bowel disease (IBD) and Familial Mediterranean Fever (FMF) are similar. Objective Here, the frequency of Mediterranean Fever (MEFV) gene mutation and its effect on the outcome of…
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Keywords:
mutation;
frequency;
disease;
gene mutation ... See more keywords
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Published in 2019 at "Digestion"
DOI: 10.1159/000502640
Abstract: Background and Aims: Familial mediterranean fever (FMF), an autoinflammatory disease, is characterized by periodic fever and serositis. An MEFV gene mutation has been identified as the cause of FMF. Recently, patients with MEFV gene mutations…
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Keywords:
inflammatory bowel;
gene;
bowel disease;
mefv gene ... See more keywords
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Published in 2023 at "Iranian Journal of Medical Sciences"
DOI: 10.30476/ijms.2022.92802.2408
Abstract: Background: In December 2019, an outbreak of pneumonia caused by the novel coronavirus disease 2019 (COVID-19) became a pandemic and caused a global health crisis. This study evaluates the immunogenic potential of the Mediterranean fever…
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Keywords:
mediterranean fever;
immunogenic potential;
mefv gene;
gene ... See more keywords
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Published in 2018 at "Turkish journal of medical sciences"
DOI: 10.3906/sag-1805-274
Abstract: Background/aim The aim of this study is to determine the ME diterranean F e V er ( MEFV ) gene mutation carrier rate in patients with glomerulonephritis and to investigate the association between disease features…
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Keywords:
carrier rate;
mefv gene;
disease;
study ... See more keywords
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Published in 2019 at "Annals of Saudi Medicine"
DOI: 10.5144/0256-4947.2019.382
Abstract: ABSTRACT BACKGROUND: Familial Mediterranean fever (FMF), an autosomal recessive, autoinflammatory disease that is common in Arabs, Jews, Armenians and Turks, is caused by mutations in the MEFV gene, which encodes a protein called pyrin. The…
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Keywords:
gene mutations;
mefv gene;
familial mediterranean;
disease ... See more keywords
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Published in 2018 at "Archivos argentinos de pediatria"
DOI: 10.5546/aap.2018.eng.e385
Abstract: OBJECTIVE To determine the frequency of the MEFV gene mutations in pediatric patients diagnosed with HSP and to assess the effect of the MEFV gene mutations on their prognosis. Material and Methods. Ccross-sectional study; pediatric…
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Keywords:
gene mutations;
mefv gene;
clinical course;
pediatric patients ... See more keywords