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http://dx.doi.org/10.3265/Nefrologia.pre2011.Dec.11157 | DOI Listing |
Clin Kidney J
September 2023
University Center of Excellence on Nephrologic, Rheumatologic and Rare Diseases (ERK-net, ERN-Reconnect and RITA-ERN Member) with Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), Coordinating Center of the Interregional Network for Rare Diseases of Piedmont and Aosta Valley, San Giovanni Bosco Hub Hospital, Turin, Italy.
J Korean Med Sci
August 2012
Division of Nephrology, Department of Internal Medicine, Sungkyunkwan University School of Medicine, Seoul, Korea.
Henoch-Schönlein purpura (HSP) is common in childhood and often self-limiting. There have been limited studies on elderly-onset HSP nephritis (HSPN). A 76-yr-old man was transferred to our hospital with a 1-month history of oliguria, abdominal pain, edema and palpable purpura in the legs.
View Article and Find Full Text PDFIntern Med
January 2013
Department of General Medicine, Flinders Medical Centre, Australia.
Azathioprine hypersensitivity is a clinical syndrome which may manifest from isolated fever and rash to multi-organ failure. This rare condition is usually self-limiting following the discontinuation of azathioprine. Therefore, it is important to maintain a high index of clinical suspicion for hypersensitivity reactions with azathioprine therapy.
View Article and Find Full Text PDFIsr Med Assoc J
February 2010
Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Background: Autoimmune neutropenia of infancy is caused by neutrophil-specific autoantibodies. Primary AIN is characterized by neutrophil count < 500 ml and a benign self-limiting course. Detecting specific antibodies against the polymorphic human neutrophil antigen usually confirms the diagnosis.
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