記事
Characteristic tubulointerstitial nephritis in IgG4-related disease
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CiNii Research
Characteristic tubulointerstitial nephritis in IgG4-related disease
- 資料種別
- 記事
- 著者
- Yutaka Yamaguchiほか
- 出版者
- Elsevier BV
- 出版年
- 2012-04
- 資料形態
- デジタル
- 掲載誌名
- Human Pathology 43 4
- 掲載ページ
- p.536-549
資料詳細
要約等:
- Nephropathy associated with IgG4-related disease is characterized by tubulointerstitial nephritis. To better identify its pathology, the present study...
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デジタル
- 資料種別
- 記事
- 出版年月日等
- 2012-04
- 出版年(W3CDTF)
- 2012-04
- タイトル(掲載誌)
- Human Pathology
- 巻号年月日等(掲載誌)
- 43 4
- 掲載巻
- 43
- 掲載号
- 4
- 掲載ページ
- 536-549
- 掲載年月日(W3CDTF)
- 2012-04
- ISSN(掲載誌)
- 00468177
- 出版事項(掲載誌)
- Elsevier BV
- 対象利用者
- 一般
- DOI
- 10.1016/j.humpath.2011.06.002
- 作成日(W3CDTF)
- 2011-09-01
- 著作権情報
- https://www.elsevier.com/tdm/userlicense/1.0/
- 関連情報(URI)
- 参照
- A condition closely mimicking IgG4-related disease despite the absence of serum IgG4 elevation and IgG4-positive plasma cell infiltrationDistribution and components of interstitial inflammation and fibrosis in IgG4-related kidney disease: analysis of autopsy specimensProposal for diagnostic criteria for IgG4-related kidney diseaseRecovery of renal function after glucocorticoid therapy for IgG4-related kidney disease with renal dysfunctionHypocomplementemia is related to elevated serum levels of IgG subclasses other than IgG4 in IgG4-related kidney diseaseLong-term changes in renal function after treatment initiation and the importance of early diagnosis in maintaining renal function among IgG4-related tubulointerstitial nephritis patients in JapanTubulointerstitial fibrosis in patients with IgG4-related kidney disease: pathological findings on repeat renal biopsyThe clinical course of patients with IgG4-related kidney diseaseMulticentric Castleman Disease With Tubulointerstitial Nephritis Mimicking IgG4-related DiseaseImmunohistological analysis for immunological response and mechanism of interstitial fibrosis in IgG4-related kidney diseaseUsefulness of gallium-67 scintigraphy for evaluating the histopathological activity in interstitial nephritisMonoclonal immunoglobulin G deposits on tubular basement membrane in renal allograft: is this significant for chronic allograft injury?Immunohistochemical Characteristics of IgG4-Related Tubulointerstitial Nephritis: Detailed Analysis of 20 Japanese CasesPrimary Sjögren's syndrome with chronic tubulointerstitial nephritis and lymphadenopathy mimicking IgG4-related diseaseClinical and biochemical characteristics of patients having general symptoms with increased serum IgG4Recent advances in IgG4-related kidney diseaseIgG4-related kidney diseaseTertiary lymphoid tissue in early‐stage IgG4-related tubulointerstitial nephritis incidentally detected with a tumor lesion of the ureteropelvic junction: a case reportComparison of clinicopathological features between patients with and without hypocomplementemia in IgG4-related kidney diseaseUltrastructural Studies of IgG4-related Kidney DiseaseIgG4関連疾患の腎病変5)IgG4 関連腎臓病・IgG4 関連後腹膜線維症Synovitis in a Patient with IgG4-related DiseaseImmunoglobulin G4-related Tubulointerstitial Nephritis with Simultaneous Resolution of Plasma Cell Infiltration and Fibrosis after Steroid Treatment自己免疫性膵炎診療ガイドライン2020
- 参照
- A case of Mikulicz’s disease complicated with interstitial nephritis successfully treated by high-dose corticosteroidTubulointerstitial nephritis associated with IgG4-related systemic diseaseAutoimmune Pancreatitis: A Systemic Immune Complex Mediated DiseaseAutoimmune PancreatitisAbundant IgG4-Positive Plasma Cell Infiltration Characterizes Chronic Sclerosing Sialadenitis (Küttner's Tumor)Analysis of IgG Immune Complexes in Sera from Patients with Membranous Nephropathy: Role of IgG4 Subclass and Low-Avidity AntibodiesChronic Tubulointerstitial Nephritis Presenting as Multiple Renal Nodules and Pancreatic InsufficiencyA new clinicopathological entity of IgG4-related autoimmune diseaseHydronephrosis associated with retroperitoneal fibrosis and sclerosing pancreatitisA case of IgG4‐related autoimmune disease with multiple organ involvementPseudotumors due to IgG4 Immune-Complex Tubulointerstitial Nephritis Associated With Autoimmune Pancreatocentric DiseaseAcute tubulointerstitial nephritis associated with autoimmune-related pancreatitisIgG4-associated idiopathic tubulointerstitial nephritis complicating autoimmune pancreatitisHigh Serum IgG4 Concentrations in Patients with Sclerosing PancreatitisA case of Mikulicz’s disease complicated with severe interstitial nephritis associated with IgG4Asian diagnostic criteria for autoimmune pancreatitis: consensus of the Japan-Korea Symposium on Autoimmune PancreatitisClinicopathological characteristics of patients with IgG4-related tubulointerstitial nephritisTubulointerstitial Nephritis Associated With IgG4-Related Autoimmune DiseaseMembranous nephropathy associated with IgG4-related systemic disease and without autoimmune pancreatitisNephropathy in IgG4-related Systemic DiseaseAutoimmune pancreatitis associated with renal lesions mimicking metastatic tumoursEndocapillary proliferative glomerulonephritis with crescent formation and concurrent tubulo-interstitial nephritis complicating retroperitoneal fibrosis with a high serum level of IgG4A case of IgG4-related tubulointerstitial nephritis showing the progression of renal dysfunction after a cure for autoimmune pancreatitisNoninfectious tubulointerstitial nephritisLymphoplasmacytic Infiltration of Multiple Organs with Immunoreactivity for IgG4: IgG4related Systemic DiseaseRenal Lesions in IgG4-Related Systemic DiseaseMembranoproliferative Glomerulonephritis-Like Glomerular Disease and Concurrent Tubulointerstitial Nephritis Complicating IgG4-Related Autoimmune PancreatitisAutoimmune Pancreatitis Associated with Various Extrapancreatic Lesions during a Long-term Clinical Course Successfully Treated with Azathioprine and Corticosteroid Maintenance Therapy
- 連携機関・データベース
- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- Crossref科学研究費助成事業データベースCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossref