Familial Mediterranean fever (Q28183734)

https://scigraph.springernature.com/pub.10.1007/s00467-003-1185-2

Europe PubMed Central

title

Familial Mediterranean fever (English)

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author name string

Aysin Bakkaloglu

series ordinal

1

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language of work or name

English

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publication date

September 2003

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published in

Pediatric Nephrology

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volume

18

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page(s)

853-9

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issue

9

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exact match

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cites work

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Acute phase response and evolution of familial Mediterranean fever

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Evolutionary study of multigenic families mapping close to the human MHC class I region

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Allogeneic bone marrow transplantation: cure for familial Mediterranean fever.

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Rapid progressive glomerulonephritis in patients with familial Mediterranean fever

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Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever.

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Ancient Missense Mutations in a New Member of the RoRet Gene Family Are Likely to Cause Familial Mediterranean Fever

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Unusual Immunologic Findings in Familial Mediterranean Fever

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Circulating immune complexes in familial Mediterranean fever, systemic lupus erythematosus and HBsAg carriers

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MEFV mutations and phenotype-genotype correlations in North African Jews and Armenians with familial Mediterranean fever

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MEFV mutations in Turkish patients suffering from Familial Mediterranean Fever

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Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

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Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever-associated vasculitis

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Periodic peritonitis, onset simultaneously with menstruation

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Thoughts on the proposed links between Behçet's disease and familial Mediterranean fever

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Familial Mediterranean fever. A survey of 470 cases and review of the literature

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Criteria for the diagnosis of familial Mediterranean fever

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Polyarteritis nodosa type vasculitis in a patient with familial Mediterranean fever treated with cyclosporin A.

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Colchicine for familial Mediterranean fever

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A Case of Familial Mediterranean Fever with Cutaneous Vasculitis and Immune Complex Nephritis: Light, Electron, and Immunofluorescent Study of Renal Biopsy

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Genotype/phenotype correlations in Arab patients with familial Mediterranean fever

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Spectrum of renal involvement in familial Mediterranean fever

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Mutation frequency of Familial Mediterranean Fever and evidence for a high carrier rate in the Turkish population

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Protracted febrile myalgia in patients with familial Mediterranean fever

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Periodic disease in Turkey

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The efficacy of interferon alpha on colchicine-resistant familial Mediterranean fever attacks: a pilot study

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Periodic fever compatible with familial Mediterranean fever

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MEFV-Gene analysis in armenian patients with Familial Mediterranean fever: diagnostic value and unfavorable renal prognosis of the M694V homozygous genotype-genetic and therapeutic implications

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Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.

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Identification of MEFV-independent modifying genetic factors for familial Mediterranean fever

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The gene for familial Mediterranean fever, MEFV, is expressed in early leukocyte development and is regulated in response to inflammatory mediators.

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Vasculitis in familial Mediterranean fever

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The spectrum of Familial Mediterranean Fever (FMF) mutations

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MEFV gene mutations in familial Mediterranean fever phenotype II patients with renal amyloidosis in childhood: a retrospective clinicopathological and molecular study

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Familial Mediterranean fever

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Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF).

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Familial Mediterranean fever--amyloidosis and the Val726Ala mutation

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The familial Mediterranean fever protein, pyrin, associates with microtubules and colocalizes with actin filaments

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Urticaria, deafness, and amyloidosis: a new heredo-familial syndrome

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Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: clinical characteristics and outcome

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Interaction of tubulin with single ring analogues of colchicine

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Prevalence of juvenile chronic arthritis and familial Mediterranean fever in Turkey: a field study.

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Colchicine Treatment in Conception and Pregnancy: Two Hundred Thirty‐one Pregnancies in Patients With Familial Mediterranean Fever

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Familial Mediterranean fever in Armenians: autosomal recessive inheritance with high gene frequency

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Familial Mediterranean fever and polyarteritis nodosa: experience of five paediatric cases. A causal relationship or coincidence?

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Successful treatment of familial Mediterranean fever attacks with thalidomide in a colchicine resistant patient.

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Colchicine: 1998 update.

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MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever

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Clinical spectrum of familial Hibernian fever: a 14-year follow-up study of the index case and extended family

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A controlled trial of colchicine in preventing attacks of familial mediterranean fever

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Familial Mediterranean fever in children: report of a large series and discussion of the risk and prognostic factors of amyloidosis

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Taiwanese patient with recurrent polyserositis: report of a case

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Familial Mediterranean fever: the genetics of inflammation

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Polyarteritis nodosa and familial Mediterranean fever: a report of 2 cases and review of the literature

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Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis

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Colchicine inhibition of chemotaxis

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Familial Mediterranean fever: clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients

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Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in Israel

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A chronic, infantile, neurological, cutaneous and articular (CINCA) syndrome. A specific entity analysed in 30 patients

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Familial Mediterranean fever: prevalence, penetrance and genetic drift

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Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis

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SErum Amyloid a Protein in Amyloidosis, Rheumatic, and Neoplastic Diseases

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Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relationships and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population.

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Familial Mediterranean fever (recurrent hereditary polyserositis) in Arabs--a study of 175 patients and review of the literature

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A candidate gene for familial Mediterranean fever

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The coexistence of familial Mediterranean fever and polyarteritis nodosa; report of a case

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Familial Mediterranean fever among the Turkish people

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12 December 2020