Results 211 to 220 of about 243,754 (245)

Idiopathic Membranous Nephropathy

Drugs, 2009
Treatment of idiopathic membranous nephropathy is based on a 'symptomatic' therapy that includes ACE inhibitors or angiotensin II receptor antagonists, and on an 'aetiological' therapy aimed at modulating underlying immunological mechanisms. The role of the latter is still debated given the usually indolent course of disease; furthermore, traditional ...
QUAGLIA, Marco, STRATTA, Piero
openaire   +3 more sources

Altered Th17/Treg ratio as a possible mechanism in pathogenesis of idiopathic membranous nephropathy.

Cytokine, 2021
Idiopathic membranous nephropathy (IMN) as a single organ autoimmune disease is a main cause of nephrotic syndrome in adults which is determined through autoantibodies to podocytes proteins.
R. Motavalli, J. Etemadi, M. Soltani-Zangbar, M. Ardalan, H. Kahroba, L. Roshangar, M. Nouri, Leili Aghebati-Maleki, F. M. Khiavi, S. Abediazar, Amir Mehdizadeh, M. Hojjat-Farsangi, A. Mahmoodpoor, Hossein Samadi Kafil, M. Zolfaghari, Javad Ahmadian Heris, M. Yousefi   +16 more
semanticscholar   +1 more source

Idiopathic membranous nephropathy in children

The Journal of Pediatrics, 1982
To determine the prognosis in children with membranous nephropathy, we reviewed the clinicopathologic features and outcome of 22 patients, 11 male and 11 female, age 11 months to 19.9 years (mean 12.0 years). Patients had biopsies within six months of onset of symptoms and were divided into two groups according to the biopsy findings: group 1 (Stages I
F, Ramirez, B H, Brouhard, L B, Travis, E N, Ellis   +3 more
openaire   +2 more sources

Therapy of idiopathic membranous nephropathy

Springer Seminars in Immunopathology, 1987
Whether and how treating idiopathic membranous nephropathy (IMN) is still a matter of debate. While there is general agreement that nonnephrotic patients should be given symptomatic treatment alone, the results of specific therapy addressed to interfere with direct or indirect causes of renal damage are controversial.
C, Ponticelli, P, Zucchelli, P, Passerini   +2 more
openaire   +2 more sources

Idiopathic membranous nephropathy in children

Pediatric Nephrology, 2006
Idiopathic membranous nephropathy (MN) is a rare cause of asymptomatic proteinuria (AP) or nephrotic syndrome (NS) in childhood. To improve our understanding of its clinical course, we retrospectively reviewed 19 cases of idiopathic MN seen in our hospital over a period of 28.5 years, i.e., from January 1977 to July 2005.
Beom Hee, Lee, Hee Yeon, Cho, Hee Gyung, Kang, Il Soo, Ha, Hae Il, Cheong, Kyung Chul, Moon, In Seok, Lim, Yong, Choi   +7 more
openaire   +2 more sources

The Clinical Course of Idiopathic Membranous Nephropathy.

Annals of Internal Medicine, 1973
Excerpt Idiopathic membranous nephropathy, well defined morphologically, is usually associated with the nephrotic syndrome and has a variable disease course.
D T, Erwin, J V, Donadio, K E, Holley
openaire   +2 more sources

Idiopathic Membranous Nephropathy

QJM: An International Journal of Medicine, 1977
Abstract The clinical and histopathological features of 37 patients with idiopathic membranous nephropathy are presented. Males were four times as commonly affected as females and the age at presentation ranged from nine to 70 years. The period of observation varied from three months to 23 years.
A M, Pierides, P, Malasit, A R, Morley, R, Willkinson, P R, Uldall, D N, Kerr   +5 more
openaire   +2 more sources

Identical twins with idiopathic membranous nephropathy

Journal of Nephrology, 2020
The pathogenesis of idiopathic membranous nephropathy is associated with autoantibodies, most often against the phospholipase A2 receptor (PLA2R) and with genetic factors, especially those involving human leukocyte antigen (HLA) genes. Idiopathic membranous nephropathy is not a typical inherited Mendelian disorder.
Tian Tao, Jue Wang, Song Lei, Zhangxue Hu   +3 more
openaire   +2 more sources

Idiopathic Membranous Nephropathy in Two Brothers

Nephron, 2008
Idiopathic membranous nephropathy has been reported rarely to develop in genetic association with certain HLA antigens. This paper describes two male siblings presenting with nephrotic syndrome with histologically proven membranous nephropathy. The younger brother maintained a normal renal function with slight proteinuria during the 3 years of follow ...
K, Sato, H, Oguchi, K, Hora, T, Furukawa, S, Furuta, H, Shigematsu, S, Yoshizawa   +6 more
openaire   +2 more sources

Idiopathic Membranous Nephropathy: Back to the Future?

Lancet, The, 2013
Giuseppe Remuzzi, Piero Ruggenenti
exaly   +3 more sources