Periodic fever syndromes

Current Opinion in Pediatrics

Volumn 12, Issue 6, 2000, Pages 563-566

  Scholl, Paul R ^a,b  

^a NORTHWESTERN UNIVERSITY   (United States)

^b Children's Mem Inst Educ and Res   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

IBUPROFEN; PARACETAMOL; PREDNISONE;

APHTHOUS STOMATITIS; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; DISEASE COURSE; DRUG RESPONSE; FAMILIAL MEDITERRANEAN FEVER; FEVER; GENETIC ASSOCIATION; HUMAN; HYPERIMMUNOGLOBULINEMIA; HYPERIMMUNOGLOBULINEMIA D AND PERIODIC FEVER SYNDROME; LYMPHADENOPATHY; NEUTROPENIA; PATHOPHYSIOLOGY; PERIODICITY; PFAPA SYNDROME; PHARYNGITIS; PRIORITY JOURNAL; RECURRENT DISEASE; REVIEW; SYNDROME; TUMOR NECROSIS FACTOR RECEPTOR ASSOCIATED PERIODIC SYNDROME;

CHILD; FAMILIAL MEDITERRANEAN FEVER; FEVER; HUMANS; PERIODICITY;

EID: 0033731122     PISSN: 10408703     EISSN: None     Source Type: Journal    
DOI: 10.1097/00008480-200012000-00009     Document Type: Review

References (32)

1. New interest in an old disease: Familial Mediterranean fever
2. Familial Mediterranean fever in children: The expanded clinical profile
3. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial Mediterranean fever: The International FMF Consortium
4. A candidate gene for familial Mediterranean fever: The French FMF Consortium
5. Mutation and haplotype studies of familial Mediterranean fever reveal new ancestral relations and evidence for a high carrier frequency with reduced penetrance in the Ashkenazi Jewish population
6. Clinical versus genetic diagnosis of familial Mediterranean fever
7. 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
8. MEFV mutation analysis in patients suffering from amyloidosis of familial Mediterranean fever
9. Phenotype-genotype correlation in familial Mediterranean fever: Evidence for an association between Met694Val and amyloidosis
10. Familial Mediterranean fever: Clinical and genetic characterization in a mixed pediatric population of Jewish and Arab patients
11. Late-onset familial Mediterranean fever (FMF): A subset with distinct clinical, demographic, and molecular genetic characteristics
12. Serum soluble intercellular adhesion molecule 1 and interleukin 8 levels in familial Mediterranean fever
13. Activation of the cytokine network in familial Mediterranean fever
14. Hematopoietic-specific expression of MEFV, the gene mutated in familial Mediterranean fever, and subcellular localization of its corresponding protein, pyrin
15. The gene for familial Mediterranean fever, MEFV, is expressed in early leukocyte development and is regulated in response to inflammatory mediators
16. Syndrome of periodic fever, pharyngitis, and aphthous stomatitis
17. Periodic fever syndrome in children
18. Periodic fever, aphthous stomatitis, pharyngitis, and adenopathy syndrome: Clinical characteristics and outcome
19. Syndrome of periodic fever, aphthous stomatitis, pharyngitis, and adenitis (PFAPA) - What it isn't. What is it?
20. Mutations in ELA2, encoding neutrophil elastase, define a 21-day biologic clock in cyclic haematopoiesis
21. Occurrence of periodic oscillations in the differential blood counts of congenital, idiopathic, and cyclical neutropenic patients before and during treatment with G-CSF
22. Hyperimmunoglobulinemia D and periodic fever: A new syndrome
23. Hyperimmunoglobulinemia D and periodic fever syndrome. The clinical spectrum in a series of 50 patients. International Hyper-IgD Study Group
24. Crescentic glomerulonephritis in hyper IgD syndrome
25. Cytokine activation during attacks of the hyperimmunoglobulinemia D and periodic fever syndrome
26. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group
27. Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulin D and periodic fever syndrome
28. Molecular cloning of human mevalonate kinase and identification of a missense mutation in the genetic disease mevalonic aciduria
29. Identification of an active site alanine in mevalonate kinase through characterization of a novel mutation in mevalonate kinase deficiency
30. Linkage of familial Hibernian fever to chromosome 12p13
31. Gene localization for an autosomal dominant familial periodic fever to 12p13
32. Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes