Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations

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Clinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/RHEUMATOLOGY/KEI279
P8608Fatcat IDrelease_grriiw4agnf6rfrid3teelkzga
P3181OpenCitations bibliographic resource ID2428791
P698PubMed publication ID16403826

P2093author name stringA Bybee
B Sengül
D R Booth
H J Lachmann
J R Gallimore
M Soytürk
M Tunca
P N Hawkins
S Akar
S E Booth
T U Yavuzşen
P2860cites workInteraction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosisQ28212112
Serum amyloid A (SAA): a concise review of biology, assay methods and clinical usefulnessQ33658740
A candidate gene for familial Mediterranean feverQ34065122
Familial Mediterranean fever: prevalence, penetrance and genetic driftQ34088721
C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart diseaseQ34311841
The spectrum of Familial Mediterranean Fever (FMF) mutationsQ34314032
Acute phase response in familial Mediterranean feverQ35550951
Familial Mediterranean fever. A survey of 470 cases and review of the literatureQ40051008
The characterization of soluble amyloid prepared in waterQ40349915
Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter studyQ40517425
Familial Mediterranean fever (FMF) mutations occur frequently in the Greek-Cypriot population of CyprusQ40576728
Clinical versus genetic diagnosis of familial Mediterranean feverQ40622322
Criteria for the diagnosis of familial Mediterranean feverQ40645936
Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosisQ40647672
Long-term colchicine treatment in children with familial mediterranean feverQ40746167
Colchicine in the prevention and treatment of the amyloidosis of familial Mediterranean feverQ40808965
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Amyloidosis as the sole manifestation of familial Mediterranean fever (FMF). Further evidence of its genetic natureQ40987119
Amyloidosis in familial Mediterranean fever. An independent genetically determined characterQ40994836
The first international standard for serum amyloid A protein (SAA). Evaluation in an international collaborative studyQ47733783
Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean FeverQ56288694
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaQ61560910
Serum amyloid-A protein concentration in inflammatory diseases and its relationship to the incidence of reactive systemic amyloidosisQ72530541
Familial Mediterranean feverQ74309346
Familial Mediterranean fever: from the clinical syndrome to the cloning of the pyrin geneQ74510628
Acute phase response and evolution of familial Mediterranean feverQ77397098
Analytical evaluation of particle-enhanced immunonephelometric assays for C-reactive protein, serum amyloid A and mannose-binding protein in human serumQ77634439
The significance of paired MEFV mutations in individuals without symptoms of familial Mediterranean feverQ78600172
CDC/AHA Workshop on Markers of Inflammation and Cardiovascular Disease: Application to Clinical and Public Health Practice: report from the laboratory science discussion groupQ81178841
P433issue6
P407language of work or nameEnglishQ1860
P921main subjectinflammationQ101991
patientQ181600
familial Mediterranean feverQ1144618
MEFV innate immuity regulator, pyrinQ11681842
negative regulation of inflammatory responseQ14861060
heterozygosityQ124059385
P304page(s)746-50
P577publication date2006-06-01
P1433published inRheumatologyQ7320492
P1476titleClinical and subclinical inflammation in patients with familial Mediterranean fever and in heterozygous carriers of MEFV mutations
P478volume45

Reverse relations

cites work (P2860)
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