ASI Standing, D Eleftheriou, HJ Lachmann… - …, 2011 - Br Soc Rheumatology Comment on: Familial Mediterranean fever caused by homozygous E148Q mutation complicated by Budd Chiari syndrome and polyarteritis nodosa: reply SIR, We thank Konstantopoulos and Kanta [1] for com- ments on our case report [2]. We agree that E148Q homo- zygosity ... Related articles - All 5 versions
ASI Standing, D Eleftheriou, HJ Lachmann… - …, 2011 - Br Soc Rheumatology Sir, FMF is an inherited disorder characterized by recurrent episodes of fever accompanied by sterile peritonitis, arthritis, pleuritis and a typical inflammatory rash [1]. The association between FMF and mutations such as M694V, M694I and V726A has been clearly established [2]; ... Cited by 3 - Related articles - All 6 versions
R Müller… - Clinical Trials in Rheumatology, 2011 - Springer Trial Treatment of Churg-Strauss syndrome without poor-prognosis factors: a multicenter, prospective, randomized, open-label study of 72 patients Substance Corticosteroid therapy: Iv pulse methylprednisolone (15 mg/kg, n = 72) Followed by oral prednisone (1 mg/kg/day) ...
JY Shin, HS Jang… - 초록집, 2011 - papersearch.net Eosinophilic fasciitis is a rare disorder with varying clinical presentations, making its clinical definition challenging. It is a scleroderma-like syndrome that was first described in 1974 by Shulman in patients with diffuse fasciitis and eosinophilia. Its onset is typically acute and findings ...
D Saadoun, B Terrier, O Semoun… - Arthritis Care & …, 2011 - Wiley Online Library Among a cohort of 161 patients with HCV-related vasculitis, 31 (19.3%) were diagnosed as having PAN. The median age was 64.5 years (interquartile range 49.5–70.5 years), with 54.8% women. Compared with HCV-associated mixed cryoglobulinemia (HCV-MC) vasculitis, ... Cited by 1 - Related articles - All 3 versions