Results 191 to 200 of about 62,770 (234)

Recurrence of immune complex and complement-mediated membranoproliferative glomerulonephritis in kidney transplantation.

Nephrology, Dialysis and Transplantation, 2022
INTRODUCTION Membranoproliferative glomerulonephritis (MPGN) represents a histologic pattern of glomerular injury which may be due to several etiologies.
F. Caravaca-Fontán, N. Polanco, B. Villacorta, Anna Buxeda, A. Coca, A. Ávila, Rocío Martínez-Gallardo, C. Galeano, R. Valero, N. Ramos, N. Allende, L. Cruzado-Vega, M. Pérez-Sáez, Á. Sevillano, E. González, Ana Hernández, E. Rodrigo, M. Fernández-Ruiz, J. Aguado, M. Valdivia, Julio Pascuall, A. Andrés, M. Praga   +22 more
semanticscholar   +1 more source

Membranoproliferative glomerulonephritis: no longer the same disease and may need very different treatment.

Nephrology, Dialysis and Transplantation, 2021
Membranoproliferative glomerulonephritis (MPGN) is a pattern of glomerular injury that may be primary or secondary to infections, autoimmune diseases and haematological disorders. Primary C3G and IC-MPGN are rare and the prognosis is unfavourable.
M. Noris, Erica Daina, G. Remuzzi
semanticscholar   +1 more source

Membranoproliferative glomerulonephritis

Nephrology Secrets, 2019
Jennifer Lopez, Howard Trachtman
openaire   +2 more sources

[Membranoproliferative glomerulonephritis].

Nihon rinsho. Japanese journal of clinical medicine, 2004
MPGN is characterized by its peculiar histological findings; lobular appearance, cellular and mesangial matrix proliferation and double contoured capillary loops. Based on histomorphalogical pattern, three types are subdivided. MPGN may be primary (in most children) or secondary (in most adults) to chronic infections, cryoglobulinemia or systemic ...
Yoshio, Taguma, Shigemi, Chiba, Hiroshi, Sato   +2 more
  +5 more sources

Familial membranoproliferative glomerulonephritis

Nephrology Dialysis Transplantation, 1995
Abstract Four and two male sibs of two separate families who had biopsy-proven membranoproliferative glomerulonephritis (MPGN) are presented. In the first family four sibs of the first-degree consanguineous marriage showed the clinical picture of nephrotic syndrome without hypocomplementaemia at initial laboratory findings.
A, Bakkaloglu, O, Söylemezoglu, K, Tinaztepe, U, Saatçi, F, Söylemezoglu   +4 more
openaire   +2 more sources

Idiopathic Membranoproliferative Glomerulonephritis

Annual Review of Medicine, 1980
Idiopathic membranoproliferative glomerulonephritis (MPGN) is one iden­ tifiable form of chronic nephritis characterized by distinctive glomerular morphology. However, it is not known whether MPGN is a single patho­ genetic entity. It was originally recognized as one type of chronic glomerulonephritis with persistent hypocomplementemia by West et al (1)
Y, Kim, A F, Michael
openaire   +2 more sources

C5 Convertase Blockade in Membranoproliferative Glomerulonephritis: A Single-Arm Clinical Trial.

American Journal of Kidney Diseases, 2019
RATIONALE & OBJECTIVE Primary membranoproliferative glomerulonephritis (MPGN) is a rare glomerulopathy characterized by complement dysregulation. MPGN progresses rapidly to kidney failure when it is associated with nephrotic syndrome.
P. Ruggenenti, Erica Daina, A. Gennarini, Camillo Carrara, S. Gamba, M. Noris, N. Rubis, Francesco Peraro, F. Gaspari, A. Pasini, A. Rigotti, R. Lerchner, D. Santoro, A. Pisani, A. Pasi, G. Remuzzi   +15 more
semanticscholar   +1 more source

Membranoproliferative glomerulonephritis.

Journal of insurance medicine (New York, N.Y.), 2005
Glomerulonephritis (GN) encompasses a wide variety of primary and secondary diseases that cause injury to the functioning unit of the kidney, the glomerulus. The many classifications of GN sometimes lead to confusion. This case study describes an individual with membranoproliferative GN and includes discussion of classification, treatment, and ...
Shuji, Kondo, Shoji, Kagami
  +6 more sources

Membranoproliferative Hypocomplementemic Glomerulonephritis

Nephron, 1973
The diagnosis of membranoproliferative glomerulonephritis is made by its distinctive glomerular morphology.
openaire   +2 more sources

IgA-dominant glomerulonephritis with a membranoproliferative pattern of injury.

Human Pathology, 2018
Immunoglobulin A (IgA)-dominant membranoproliferative glomerulonephritis (MPGN) is a descriptive term for renal biopsies in which differential diagnoses of unusual IgA nephropathy (IgAN), infection-related GN, or other etiologies are considered.
Nicole K. Andeen, J. A. Jefferson, Shreeram Akilesh, C. Alpers, M. Bissonnette, L. Finn, J. Higgins, D. Houghton, N. Kambham, A. Magil, Behzad Najafian, R. Nicosia, M. Troxell, Kelly D. Smith   +13 more
semanticscholar   +1 more source