Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups.
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Type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi JewsThe Pathogenesis of Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Cervical Adenitis Syndrome: A Review of Current ResearchInteraction between pyrin and the apoptotic speck protein (ASC) modulates ASC-induced apoptosisPredominant role of host genetics in controlling the composition of gut microbiota.Familial mediterranean Fever: a retrospective clinical and molecular study in the East of anatolia region of Turkey.Usefulness of mean platelet volume and neutrophil-to-lymphocyte ratio for evaluation of children with Familial Mediterranean fever.Pathogenesis of familial periodic fever syndromes or hereditary autoinflammatory syndromes.MEFV mutations in Northwest of Iran: a cross sectional studyE148Q is a disease-causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean feverSevere disease in patients with rheumatoid arthritis carrying a mutation in the Mediterranean fever gene.Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean fever.Assessment of MEFV Gene Mutations in Exon 10 in Familial Mediterranean Fever Patients from Iranian Azeri and Turkish Population.Prevalence and significance of mutations in the familial Mediterranean fever gene in patients with Crohn's disease.CATERPILLERs, pyrin and hereditary immunological disorders.High prevalence of spondyloarthritis and ankylosing spondylitis among familial Mediterranean fever patients and their first-degree relatives: further evidence for the connection.The risk of familial Mediterranean fever in MEFV heterozygotes: a statistical approachMonogenic autoinflammatory diseases: concept and clinical manifestations.Colchicine-free remission in familial Mediterranean fever: featuring a unique subset of the disease-a case control study.Familial Mediterranean fever--a review.Clinical Review: Familial Mediterranean Fever-An Overview of Pathogenesis, Symptoms, Ocular Manifestations, and Treatment.The differential contribution of MEFV mutant alleles to the clinical profile of familial Mediterranean fever.Common MEFV mutations among Jewish ethnic groups in Israel: high frequency of carrier and phenotype III states and absence of a perceptible biological advantage for the carrier state.Aortic Flow Propagation Velocity in Patients with Familial Mediterranean Fever: an Observational Study.Evidence of digenic inheritance in autoinflammation-associated genes.Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.A case report of cutaneous polyarteritis nodosa in siblings.Patient with FMF and Triple MEFV Gene Mutations.Familial Mediterranean fever associated with MEFV mutations in a large cohort of Cypriot patients.Diagnostic validity of colchicine in patients with Familial Mediterranean fever.MEFV gene mutations in Henoch-Schönlein purpura.Exertional leg pain as a manifestation of occult spondyloarthropathy in familial Mediterranean fever: an MRI evaluation.Familial Mediterranean FeVer gene (MEFV) mutations as a modifier of systemic lupus erythematosus.Common MEFV mutations in Iranian Azeri Turkish patients with Behçet's disease.MEFV mutation carriage in Israeli Jewish individuals from ethnicities with low risk for familial Mediterranean fever.Prevalence of known mutations in the familial Mediterranean fever gene (MEFV) in various carrier screening populations.Common FMF alleles may predispose to development of Behcet's disease with increased risk for venous thrombosis.Familial Mediterranean fever among patients from Karabakh and the diagnostic value of MEFV gene analysis in all classically affected populations.Common mutations in the familial Mediterranean fever gene associate with rapid progression to disability in non-Ashkenazi Jewish multiple sclerosis patients.Familial Mediterranean fever: the segregation of four different mutations in 13 individuals from one inbred family: genotype-phenotype correlation and intrafamilial variability.An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome.
P2860
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P2860
Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups.
description
2000 nî lūn-bûn
@nan
2000年の論文
@ja
2000年学术文章
@wuu
2000年学术文章
@zh-cn
2000年学术文章
@zh-hans
2000年学术文章
@zh-my
2000年学术文章
@zh-sg
2000年學術文章
@yue
2000年學術文章
@zh
2000年學術文章
@zh-hant
name
Higher than expected carrier r ...... various Jewish ethnic groups.
@en
Higher than expected carrier r ...... various Jewish ethnic groups.
@nl
type
label
Higher than expected carrier r ...... various Jewish ethnic groups.
@en
Higher than expected carrier r ...... various Jewish ethnic groups.
@nl
prefLabel
Higher than expected carrier r ...... various Jewish ethnic groups.
@en
Higher than expected carrier r ...... various Jewish ethnic groups.
@nl
P2093
P356
P1476
Higher than expected carrier r ...... various Jewish ethnic groups.
@en
P2093
G J Halpern
N Stoffman
Y Lifshitz
P2888
P304
P356
10.1038/SJ.EJHG.5200446
P577
2000-04-01T00:00:00Z