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Variants of Alport's syndrome
Variants of Alport's syndrome include mainly those associated with hereditary macrothrombocytopenia (and occasionally leukocyte inclusions) or with esophageal, tracheobronchial and genital leiomyomatosis. With...
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Unusual sites of Salmonella osteoarthritis in patients with sickle cell disease: two cases
Salmonella osteoarticular infections involve mainly long bones such as the femur, tibia, and humerus in patients with sickle cell disease (SCD). We report here two unusual cases of Salmon...
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Is procalcitonin a marker of invasive bacterial infection in acute sickle-cell vaso-occlusive crisis?
Fever is often present during painful vaso-occlusive crisis (VOC) in sickle-cell disease (SCD), but does not always indicate infection. The aim of our study was to test procalcitonin as a marker of invasive ba...
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Open AccessPW02-016 - 41 cases of TRAPS, a rare autoinflammatory disease
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Open AccessOR2-002 – The risk of FMF in MEFV heterozygotes
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Open AccessPW01-022 – Dissociation between CRP and SAA in FMF
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Open AccessPW03-034 – How to classify autoinflammatory diseases?
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Open AccessPReS-FINAL-2231: A series of 41 mutations of TNFRAF1A
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Open AccessFrench Amyloidosis CAPS study: AA Amyloidosis complicating cryopyrin-associated periodic syndrome: a study on 14 cases and review of 53 cases from literature
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Open AccessChronic myelomonocytic leukemia as a cause of fatal uncontrolled inflammation in familial Mediterranean fever
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Open Access“Daily life of CAPS patients treated with canakinumab (Ilaris®) : data from the French observational study - ENVOL Study”
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Open AccessRecommendations for the management of autoinflammatory diseases
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Open AccessVasculitis associated with familial Mediterranean fever: a study on 16 french adult cases
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Open AccessHidradenitis suppurativa and familial Mediterranean fever: a report of 6 cases and literature review