CS Capannini

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Address: 1Department of Biomedicine, Division of Rheumatology, Transition Unit, University of Florence, Florence, Italy, 2Department of Paediatrics, Rheumatology Unit, University of Padua, Padua, Italy, 3Department of Paediatrics, Rheumatology Unit, University of Messina, Messina, Italy and 4A. Meyer Children's Hospital, Rheumatology Unit, University of(More)
Methods The study population included 162 pts (113 F and 49 M, mean age 10.6 ± 3.1 yrs) affected with JIA: 77 oligoarticular, 48 polyarticular RF-, 15 systemic, and 22 enthesitisrelated arthritis (ERA) onset. All patients underwent bone mass evaluation by DXA at lumbar spine (L2–L4). DXA values were correlated with JIA category, age at onset, disease(More)
Patients The boy developed at 8 yrs musculoskeletal pain and painful nodules on the legs, than vertigo, tinnitus, and diplopia, neurosensorial ipoacusia, left central facial palsy and hypertension. Angio MRI revealed ischemic alterations on Willis's circle and prompted to diagnose PAN. Despite aggressive therapy the boy developed ischemic lesions of 3(More)
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