Familial mediterranean fever;Fièvre méditerranéenne familiale

Revue du Praticien

Volumn 52, Issue 2, 2002, Pages 149-154

  Cattan, Daniel ^a   Dervichian, Michel ^a  

^a Centre Hospitalier Intercommunal   (France)

Author keywords

[No Author keywords available]

Indexed keywords

COLCHICINE;

AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 16; ENDEMIC DISEASE; FAMILIAL MEDITERRANEAN FEVER; FEVER; GENE LOCATION; GENE MUTATION; INFLAMMATION; KIDNEY AMYLOIDOSIS; MALARIA; PROPHYLAXIS; REVIEW; RHEUMATIC FEVER;

AMYLOIDOSIS; ANTI-INFLAMMATORY AGENTS; CHROMOSOMES, HUMAN, PAIR 16; ETHNIC GROUPS; FAMILIAL MEDITERRANEAN FEVER; HUMANS; MALARIA; PAIN; PERIODICITY; PROGNOSIS; TUBERCULOSIS;

EID: 0037081152     PISSN: 00352640     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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2. La maladie périodique (sur 14 cas personnels dont 8 compliqués de néphropathie)
3. Maladie périodique amylogène
4. Familial mediterranean fever
5. A new approach to the treatment of periodic fever
6. Colchicine for familial mediterranean fever
7. Colchicine in the prevention and treatment of amyloidosis of familial mediterranean fever
8. Mapping of a gene causing familial mediterranean fever to the short arm of chromosome 16
9. A candidate gene for familial mediterranean fever
10. Ancient missense mutations in a new member of the RoRet gene family are likely to cause familial mediterranean fever
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12. Mutations in the MEFV gene in a large series of patients with a clinical diagnosis of familial mediterranean fever
13. The MICA region determines the first modifier locus in familial mediterranean fever
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17. MEFV mutations in Beḩet's disease
18. A single mutated MEFV allele in Israeli patients suffering from familial mediterranean fever and Beḩet's disease (FMF-BD)
19. Prevalence of juvenile chronic arthritis and familial mediterranean fever in Turkey: A field study
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21. Clinical, laboratory and molecular characteristics of children with familial mediterranean fever-associated vasculitis