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Familial antiglomerular basement membrane disease in zero human leukocyte antigen mismatch siblings
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Angioi A, Cheungpasitporn W, Sethi S, De Vriese AS, Lepori N, Schwab TR, Fervenza FC. Angioi A, et al. Clin Nephrol. 2017 Nov;88(11):277-283. doi: 10.5414/CN109206. Clin Nephrol. 2017. PMID: 28853702
Despite severe acute kidney injury requiring hemodialysis, the patient responded well to the standard therapy with cyclophosphamide, plasmapheresis, and systemic corticosteroids. At her 3-month follow-up visit, the patient's kidney functions had recovered, and hemodialysis …
Despite severe acute kidney injury requiring hemodialysis, the patient responded well to the standard therapy with cyclophosphamide, plasmap …
An unusual presentation of childhood vasculitis presenting in adulthood: a challenging diagnosis of henoch-schönlein purpura.
Thongprayoon C, Cheungpasitporn W, Thamcharoen N, Bruminhent J. Thongprayoon C, et al. N Am J Med Sci. 2014 Oct;6(10):543-4. doi: 10.4103/1947-2714.143289. N Am J Med Sci. 2014. PMID: 25489569 Free PMC article.
She continued to do well with normal kidney function at a 3-month follow-up visit. CONCLUSION: HSP, a systemic IgA vasculitis, is a predominantly pediatric vasculitis and is uncommon in adults. ...
She continued to do well with normal kidney function at a 3-month follow-up visit. CONCLUSION: HSP, a systemic IgA vasculitis, is a p …