Proposal for diagnostic criteria for IgG4-related kidney disease
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- Material Type
- 記事
- Author/Editor
- Mitsuhiro KawanoTakako SaekiHitoshi Nakashima
- Publication, Distribution, etc.
- Publication Date
- 2011-09-07
- Publication Date (W3CDTF)
- 2011-09-07
- Periodical title
- Clinical and experimental nephrology : official publication of the Japanese Society of Nephrology
- No. or year of volume/issue
- 15(5)
- Volume
- 15(5)
- ISSN (Periodical Title)
- 1437-7799
- ISSN-L (Periodical Title)
- 1437-7799
- Text Language Code
- eng
- DOI
- 10.1007/s10157-011-0521-2
- Persistent ID (NDL)
- info:ndljp/pid/11553498
- Collection
- Collection (Materials For Handicapped People:1)
- Collection (particular)
- 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- Acquisition Basis
- オンライン資料収集制度
- Date Accepted (W3CDTF)
- 2020-10-08T21:45:28+09:00
- Date Captured (W3CDTF)
- 2020-06-16
- Format (IMT)
- application/pdf
- Access Restrictions
- 国立国会図書館内限定公開
- Service for the Digitized Contents Transmission Service
- 図書館・個人送信対象外
- Availability of remote photoduplication service
- 可
- Periodical Title (URI)
- Periodical Title (Persistent ID (NDL))
- info:ndljp/pid/11553497
- Data Provider (Database)
- 国立国会図書館 : 国立国会図書館デジタルコレクション
- Summary, etc.
- コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > その他
- DOI
- 10.1007/s10157-011-0521-2
- Access Restrictions
- インターネット公開
- Related Material (URI)
- Is Referenced By
- A condition closely mimicking IgG4-related disease despite the absence of serum IgG4 elevation and IgG4-positive plasma cell infiltrationFactors related to renal cortical atrophy development after glucocorticoid therapy in IgG4-related kidney disease: a retrospective multicenter study.Distribution and components of interstitial inflammation and fibrosis in IgG4-related kidney disease: analysis of autopsy specimensAssociation of serum levels of fibrosis-related biomarkers with disease activity in patients with IgG4-related diseaseUtility of gastric biopsy in diagnosing IgG4‐related gastrointestinal diseaseClinical and histological changes associated with corticosteroid therapy in IgG4-related tubulointerstitial nephritisConsensus statement on the pathology of IgG4-related diseaseCurrent approach to the diagnosis of IgG4-related disease – Combination of comprehensive diagnostic and organ-specific criteriaAre Classification Criteria for IgG4-RD Now Possible? The Concept of IgG4-Related Disease and Proposal of Comprehensive Diagnostic Criteria in JapanClinical Outcomes After Endovascular Repair and Open Surgery to Treat Immunoglobulin G4–Related and Nonrelated Inflammatory Abdominal Aortic AneurysmsHypocomplementemia is related to elevated serum levels of IgG subclasses other than IgG4 in IgG4-related kidney diseaseDifferent factors underlie recurrent and de novo organ involvement in immunoglobulin G4–related diseaseThe 2020 revised comprehensive diagnostic (RCD) criteria for IgG4-RDLong-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 JapanAmendment of the Japanese consensus guidelines for autoimmune pancreatitis, 2020Development of IgG4-related pancreatitis and kidney disease 7 years after the onset of undiagnosed lymphadenopathy: A case reportInternational Consensus Guidance Statement on the Management and Treatment of IgG4‐Related DiseaseA proposal of a diagnostic algorithm with validation of International Consensus Diagnostic Criteria for autoimmune pancreatitis in a Japanese cohortIgG4-related diseaseIgG4-related disease and its pathogenesis—cross-talk between innate and acquired immunityCutoff Values of Serum IgG4 and Histopathological IgG4+ Plasma Cells for Diagnosis of Patients with IgG4-Related DiseaseNew clues to the nature of immunoglobulin G4-related disease: a retrospective Japanese multicenter study of baseline clinical features of 334 casesAssociation Between Immunoglobulin G4–related Disease and Malignancy within 12 Years after Diagnosis: An Analysis after Longterm FollowupTubulointerstitial fibrosis in patients with IgG4-related kidney disease: pathological findings on repeat renal biopsyA suspected case of coronary periarteritis due to IgG4-related disease as a cause of ischemic heart diseaseA case of IgG4-related tubulointerstitial nephritis and membranous glomerulonephritis during the clinical course of gastric cancer: Imaging features of IgG4-related kidney diseaseMulticentric Castleman Disease With Tubulointerstitial Nephritis Mimicking IgG4-related DiseaseProgressive Renal Dysfunction due to IgG4-Related Kidney Disease Refractory to Steroid Therapy: A Case ReportIgG4-positive cell infiltration in various cardiovascular disorders - results from histopathological analysis of surgical samplesClinical features of IgG4-related periaortitis/periarteritis based on the analysis of 179 patients with IgG4-related disease: a case–control studyChanges in N-glycans of IgG4 and its relationship with the existence of hypocomplementemia and individual organ involvement in patients with IgG4-related diseaseImmunohistological analysis for immunological response and mechanism of interstitial fibrosis in IgG4-related kidney diseaseValidation of the comprehensive diagnostic criteria for IgG4-related disease in a SMART registryInvolvement of two or more sets of lacrimal glands and/or major salivary glands is related to greater systemic disease activity due to multi-organ involvement in IgG4-related dacryoadenitis/sialadenitisPositive disease-specific autoantibodies have limited clinical significance in diagnosing IgG4-related disease in daily clinical practiceIs serum cholinesterase level a predictor of the extent of organ involvement in immunoglobulin G4-related disease?IgG4-IgE complex in a patient with IgG4-related diseaseSerum free light chain assessment in type 1 autoimmune pancreatitisClinical profile of IgG4-related disease in Japan based on the rare disease data registryA case of IgG4-related lymphadenopathy, pericarditis, coronary artery periarteritis and luminal stenosisCurrent concept and diagnosis of IgG4-related disease in the hepato-bilio-pancreatic systemGastrointestinal manifestation of immunoglobulin G4-related disease: clarification through a multicenter surveyDistinct cytokine mRNA expression pattern in immunoglobulin G4-related kidney disease associated with renal cell carcinomaImmunohistochemical Characteristics of IgG4-Related Tubulointerstitial Nephritis: Detailed Analysis of 20 Japanese CasesPrimary Sjögren's syndrome with chronic tubulointerstitial nephritis and lymphadenopathy mimicking IgG4-related diseaseA case developing minimal change disease during the course of IgG4-related diseaseRenal Involvement in Retroperitoneal Fibrosis: Prevalence, Impact and Management ChallengesValidation of the 2019 ACR/EULAR criteria for IgG4-related disease in a Japanese kidney disease cohort: a multicentre retrospective study by the IgG4-related kidney disease working group of the Japanese Society of NephrologyRecent advances in IgG4-related kidney diseaseCase Report: IgG4-related kidney disease complicated by interstitial pneumoniaImproved Renal Function in Initial Treatment Improves Patient Survival, Renal Outcomes, and Glucocorticoid-Related Complications in IgG4-Related Kidney Disease in JapanDiagnosis and classification of autoimmune pancreatitisProposed diagnostic criteria for IgG4-related respiratory diseaseGlucocorticoid receptor expression in resident and hematopoietic cells in IgG4-related diseaseClinical course after corticosteroid therapy in IgG4-related aortitis/periaortitis and periarteritis: a retrospective multicenter studyAbundant a proliferation-inducing ligand (APRIL)-producing macrophages contribute to plasma cell accumulation in immunoglobulin G4-related diseasePathogenicity of IgG in patients with IgG4-related diseaseCT Findings of Upper Urinary Tract Lesions in IgG4-Related Disease: Comparison With Urothelial CarcinomaIgG4-related disease: Changing epidemiology and new thoughts on a multisystem diseaseTertiary lymphoid tissue in early‐stage IgG4-related tubulointerstitial nephritis incidentally detected with a tumor lesion of the ureteropelvic junction: a case reportA case of eosinophilic granulomatosis with polyangiitis as a mimicker of IgG4-related diseaseSerum IgG4 levels at diagnosis can predict unfavorable outcomes of untreated patients with IgG4-related diseaseNationwide epidemiological survey of immunoglobulin G4‐related disease with malignancy in JapanPerformance of classification and diagnostic criteria for IgG4-related disease and comparison of patients with and without IgG4-related diseaseComparison of clinicopathological features between patients with and without hypocomplementemia in IgG4-related kidney diseaseAutoimmune Pancreatitis and IgG4-Related Disease: The Storiform Discovery to TreatmentClinicopathological differential diagnosis of IgG4‐related disease: A historical overview and a proposal of the criteria for excluding mimickers of IgG4‐related diseaseIgG4-related pleural disease with aortitis and submandibular glands involvement successfully treated with corticosteroid: case-based reviewDiagnostic criteria for IgG4-related ophthalmic diseaseCorticosteroid Therapy for a Patient with Relapsing Polychondritis Complicated by IgG4-Related DiseaseIgG4関連疾患の診断マーカーと治療マーカーとしての血清IgG4値測定の有用性IgG4-Related Disease: Diagnostic Methods and Therapeutic Strategies in JapanUltrastructural Studies of IgG4-related Kidney Disease5)IgG4 関連腎臓病・IgG4 関連後腹膜線維症IgG4-related Dacryoadenitis and Sialadenitis with Palatal Gland SwellingIgG4関連疾患の病態および診断と治療IgG4-related Disease: Recent Topics on Immunological Aspects of This Disorder and Their Application in New Treatment StrategiesPossible IgG4-Related Kidney Disease Requiring a Differential Diagnosis of Membranous Lupus NephritisA New Clinical Entity: IgG4-Related Disease (IgG4-RD) Discovered in the 21st CenturyMyeloperoxidase Antineutrophil Cytoplasmic Antibody (MPO-ANCA) Associated Crescentic and Necrotizing Glomerulonephritis (GN) with Membranoproliferative GN FeaturesIgG4-related Disease - A Systemic Disease that Deserves Attention Regardless of One's SubspecialtyIgG4-related Disease: A Mass Lesion in the Intrarenal Sinus near the Renal PelvisIgG4-related Disease Involving Multiple Organs with Elevated Serum Interleukin-6 LevelsPericardial Involvement in IgG4-related DiseaseIgG4-related Kidney Disease in Which the Urinalysis, Kidney Function and Imaging Findings Were Normal他科に学ぶ自己免疫疾患1.尿異常から腎生検までDevelopment of Nephritis and Abnormal Lung Shadow in a Patient with IgG4-related Hypertrophic Pachymeningitis with MPO-ANCA Positivity after Unplanned Interruption of Maintenance Glucocorticoid TherapyDevelopment of Myeloperoxidase Anti-neutrophil Cytoplasmic Antibody-positive Necrotizing Crescentic Glomerulonephritis in an Elderly Patient with Immunological Kidney Disease2020年 改訂 IgG4関連疾患包括診断基準―The 2020 Revised Comprehensive Diagnostic(RCD)Criteria for IgG4-RD ―厚生労働省難治性疾患等政策研究事業 IgG4関連疾患の診断基準並びに診療指針の確立を目指す研究班Immunoglobulin G4-related Tubulointerstitial Nephritis with Simultaneous Resolution of Plasma Cell Infiltration and Fibrosis after Steroid Treatment新たなIgG4関連疾患診断基準―2020改訂IgG4関連疾患包括診断基準とThe 2019 ACR/EULAR classification criteria for IgG4-related diseaseAn Atypical Cystic Renal Mass in a Patient with IgG4-Related Kidney DiseaseIgG4-Positive Plasmacytic Infiltration in Aortic Wall and Aortic Valve Surgical Samples and Its Relation to Preoperative Serum IgG4 LevelsRefractory Eosinophilic Granulomatosis with Polyangiitis Complicated with IgG4-related Disease Showing Different Treatment Responses for Each OrganProposal of diagnostic criteria for IgG4-related thyroid disease自己免疫性膵炎診療ガイドライン2020CLINICAL INVESTIGATION : A prevalence study of IgG4-related ophthalmic disease in JapanValidation of the diagnostic criteria for IgG4-related kidney disease (IgG4-RKD) 2011, and proposal of a new 2020 versionA case of IgG4-related kidney disease with predominantly unilateral renal atrophyLow-density lipoprotein apheresis for PLA2R-related membranous glomerulonephritis accompanied by IgG4-related tubulointerstitial nephritis
- References
- Characteristic findings in images of extra-pancreatic lesions associated with autoimmune pancreatitisRenal cortical lesions in patients with autoimmune pancreatitis: A clue to differentiation from pancreatic malignancyA case of Mikulicz’s disease complicated with interstitial nephritis successfully treated by high-dose corticosteroidWegener’s granulomatosis presenting as renal mass: A case for nephron-sparing surgeryDiagnosis of Autoimmune Pancreatitis: The Mayo Clinic ExperienceCharacteristic tubulointerstitial nephritis in IgG4-related diseaseHistopathologic and Clinical Subtypes of Autoimmune Pancreatitis: The Honolulu Consensus DocumentAutoimmune Pancreatitis: A Systemic Immune Complex Mediated DiseaseIgG4-Related DiseaseNumerous IgG4-positive plasma cells are ubiquitous in diverse localised non-specific chronic inflammatory conditions and need to be distinguished from IgG4-related systemic disordersRenal lesions associated with autoimmune pancreatitis: CT findingsChronic Tubulointerstitial Nephritis Presenting as Multiple Renal Nodules and Pancreatic InsufficiencyQuality of life following high‐intensity focused ultrasound for the treatment of localized prostate cancer: A prospective studyWegener’s Granulomatosis Presenting as a Renal MassAutoimmune pancreatitis and IgG4-related sclerosing diseaseA case of IgG4‐related autoimmune disease with multiple organ involvementSubclassification of Autoimmune PancreatitisPseudotumors 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 PancreatitisAsian diagnostic criteria for autoimmune pancreatitis: consensus of the Japan-Korea Symposium on Autoimmune PancreatitisAn abundance of IgG4+ plasma cells is not specific for IgG4-related tubulointerstitial nephritisClinicopathological 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 pancreatitisProposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disordersAbdominal extrapancreatic lesions associated with autoimmune pancreatitis: Radiological findings and changes after therapyNephropathy in IgG4-related Systemic DiseaseAutoimmune pancreatitis associated with renal lesions mimicking metastatic tumoursClinical diagnostic criteria of autoimmune pancreatitis: revised proposalElevated IgG4 concentrations in serum of patients with Mikulicz's diseaseClinical Characteristics of 327 Asian Patients With Autoimmune Pancreatitis Based on Asian Diagnostic CriteriaInternational Consensus Diagnostic Criteria for Autoimmune PancreatitisRenal Involvement in Patients with Autoimmune Pancreatitis: CT and MR Imaging FindingsSarcoidosis Associated with Renal Masses on Computed TomographyAnalysis of serum IgG subclasses in Churg-Strauss syndrome—the meaning of elevated serum levels of IgG4IgG4-related Tubulointerstitial Nephritis and Hepatic Inflammatory Pseudotumor without Hypocomplementemia自己免疫性膵炎臨床診断基準2006の解説‐3.血清学的診断‐Membranoproliferative Glomerulonephritis-Like Glomerular Disease and Concurrent Tubulointerstitial Nephritis Complicating IgG4-Related Autoimmune PancreatitisIgG4-related Chronic Tubulointerstitial Nephritis without Autoimmune Pancreatitis and the Time Course of Renal FunctionAutoimmune Pancreatitis Associated with Various Extrapancreatic Lesions during a Long-term Clinical Course Successfully Treated with Azathioprine and Corticosteroid Maintenance Therapy
- Data Provider (Database)
- 国立情報学研究所 : CiNii Research
- Original Data Provider (Database)
- 雑誌記事索引データベースCrossref科学研究費助成事業データベース科学研究費助成事業データベース科学研究費助成事業データベース科学研究費助成事業データベースCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossref
- Bibliographic ID (NDL)
- 11553498