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1. ヘノッホ・シェーンライン紫斑病 (IgA血管炎)の腎症状 renal manifestations of henoch schonlein purpura iga vasculitis
2. ヘノッホ・シェーンライン紫斑病（IgA血管炎）：臨床症状および診断 henoch schonlein purpura immunoglobulin a vasculitis clinical manifestations and diagnosis
3. 小児における糸球体腎炎の病因と原因の概要 overview of the pathogenesis and causes of glomerulonephritis in children

Outcome of Henoch-Schönlein purpura 8 years after treatment with a placebo or prednisone at disease onset.

Jauhola O, Ronkainen J, Koskimies O, Ala-Houhala M, Arikoski P, Hölttä T, Jahnukainen T, Rajantie J, Örmälä T, Nuutinen M.SourceDepartment of Children and Adolescents, Oulu University Hospital, PO Box 23, 90029, Oulu, Finland.
Pediatric nephrology (Berlin, Germany).Pediatr Nephrol.2012 Jun;27(6):933-9. Epub 2012 Feb 5.
BACKGROUND: Corticosteroids have been shown not to prevent the development of Henoch-Schönlein nephritis. However, long-term follow-up data are scarce.METHODS: The long-term outcome of patients in a randomized placebo-controlled prednisone study was evaluated 8 years later with a health questionnai
PMID 22311342

Increased Serum Concentration of Sphingosine-1-phosphate in Juvenile-onset Systemic Lupus Erythematosus.

Watson L, Tullus K, Marks SD, Holt RC, Pilkington C, Beresford MW.SourceDepartment of Women's and Children's Health, Institute of Translational Medicine, University of Liverpool, Alder Hey Children's NHS Foundation Trust Hospital, Eaton Road, Liverpool, L12 2AP, UK, louise.watson@liverpool.ac.uk.
Journal of clinical immunology.J Clin Immunol.2012 May 31. [Epub ahead of print]
PURPOSE: Sphingosine-1-phosphate (S1P) is an active sphingolipid with chemotactic abilities and has been linked to inflammatory mediators and autoimmune disease. The aim of this study was to assess whether children with juvenile-onset systemic lupus erythematosus (JSLE) express increased systemic an
PMID 22648459

服部元史
日本アフェレシス学会雑誌 30(2), 90-96, 2011-05-31
… In this article, the efficacy of plasmapheresis and possible mechanisms of action of plasmapheresis in renal diseases, especially focusing on 1) a rapidly progressive type of Henoch-Schonlein purpura nephritis (HSPN), 2) steroid-resistant primary focal segmental glomerulosclerosis (FSGS) and 3) post-transplant recurrence of FSGS are reviewed. …
NAID 110008661247

津田匠,濱田吉則,高田晃平,權雅憲
日本小児外科学会雑誌 47(2), 237-241, 2011-04-20
… Henoch-Schonlein紫斑病(本症)はIgA型免疫複合体が全身の細静脈に沈着して引き起こされる血管炎で,臨床的には皮膚症状,関節症状,腹部症状を3主徴とする非血小板減少性の紫斑病である.合併症としては腸重積.腎炎などがあるが,腸重積は1.3?13.6%の割合で認められ外科的治療を必要とすることもある.乳児でみられる特発性腸重積症は小腸結腸型が多いのに比べて,本症に合併する腸重積症はその約半数が小 …
NAID 110008607766