نتایج جستجو برای: iga glomerulonephritis

تعداد نتایج: 36253  

Journal: :Japanese journal of medicine 1984
M Hatano

Clinical Studies on Primary Glomerular Disease The purpose of this study can be divided into two main categories: I) recent study of the mechanism of development of primary glomerular disease and II) recent problems in the treatment of advanced glomerular disease. I. The morbid types and development of primary glomerular disease Classification of primary glomerular disease has been studied by m...

Journal: :The Malaysian journal of pathology 2001
J J Khoo

Consecutive renal biopsies received from 1994 to 2000 in Johor Bahru were reviewed. There were 441 cases, of which 407 were adequate biopsies (92.3%). Lupus nephritis formed the largest diagnostic entity (126 cases, 31.0%). This reflected the high prevalence of systemic lupus erythematosus (SLE) patients in Malaysia. The most common histological pattern of lupus nephritis was diffuse proliferat...

Journal: :Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2006
Paisal Parichatikanond Ratana Chawanasuntorapoj Chairat Shayakul Boonyarit Choensuchon Somkiat Vasuvattakul Kriengsak Vareesangthip Thawee Chanchairujira Suchai Sritippayawan Attapong Vongwiwatana Nalinee Premasathian Kraiwiporn Kiattisunthorn Ratana Larpkitkachorn Leena Ongajyooth

BACKGROUND The knowledge of the epidemiology of biopsied renal diseases provides useful information in clinical practice. There are several epidemiologic population-based studies of biopsy-proven nephropathies with detailed clinicopathologic correlations that could be different according to the country analyzed. OBJECTIVE To identify the prevalence of primary and secondary glomerular diseases...

Journal: :Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998
J Soma T Saito T Ootaka H Sato K Abe

BACKGROUND An important aspect in glomerular nephritic processes is the enhanced influx of leukocytes into the glomerulus. METHODS To investigate the mechanisms of intraglomerular leukocyte infiltration in IgA nephropathy (IgA-N) and membranoproliferative glomerulonephritis type I (MPGN-I), we immunohistochemically examined the intraglomerular expression of leukocyte function-associated antig...

Journal: :Seminars in nephrology 2003
Jun Wada Hitoshi Sugiyama Hirofumi Makino

Immunoglobulin A (IgA) nephropathy is an immune-complex-mediated glomerulonephritis characterized by the presence of immunoglobulin A deposits in mesangial and paramesangial regions. The patients with IgA nephropathy present with varying clinical symptoms (eg, microhematuria with preserved renal function or progressive deterioration of renal functions resulting in end-stage renal disease). The ...

Journal: :Chest 2021

TOPIC: Critical Care TYPE: Medical Student/Resident Case Reports INTRODUCTION: Staphylococcus-associated glomerulonephritis (SAGN) is an immune complex–mediated (GN) which commonly presents with elevated creatinine, microscopic hematuria, and variable proteinuria; but on rare occasions may manifest as vasculitis that closely mimics Henoch-Schonlein Purpura (HSP). CASE PRESENTATION: A 62-year-ol...

دکتر احمدعلی نیکی‌بخش, , دکتر علی آقایار ماکوئی, , دکتر محمد کرمی‌یار, , دکتر مهران نوروزی, , دکتر هاشم محمودزاده, ,

 Received: 18 Aug, 2008 Accepted: 14 Feb, 2009  Abstract  Renal involvement is one of the most serious sequela of Henoch-Schönlein purpura. The presence of proteinuria (nephritic range) and hematuria is also associated with progression to renal insufficiency. In fifty percent of patients who display a combination of nephritis-nephrotic symptoms, end-stage disease develops. Pharmacologic treatme...

Journal: :Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation 2005
William Couser

Glomerular diseases, including diabetes and various forms of glomerulonephritis, account for more than 70% of patients undergoing renal transplantation. Among these patients, more than 40% develop significant proteinuria, and around 15% develop persistent nephrotic syndrome. The most common cause of posttransplantation proteinuria is chronic allograft nephropathy (60%), followed by recurrent (1...

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