Results 171 to 180 of about 28,785 (230)
Ophthalmic Manifestations Heralding Renal Pathology: A Rare Case of Bilateral Optic Disc Edema with Exudative Maculopathy in IgA Nephropathy. [PDF]
Case Rep OphthalmolBhavsar D +5 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
IgA‐Associated Glomerulonephritis
Australian and New Zealand Journal of Medicine, 1975Summary: Mesangial IgA deposition was detected by routine fluorescent microscopy of 19 cases of glomerulonephritis.Twelve patients had a variable degree of diffuse mesangial proliferative glomerulonephritis. The heterogeneous histological findings in the other seven patients show that mesangial IgA deposition alone does not have diagnostic specificity.
A J, Woodroffe +3 more
openaire +2 more sources
International Urology and Nephrology, 1979
Renal biopsy specimens from 204 patients with glomerulonephritis or nephrotic syndrome have been studied. In ten of the patients not suffering from acute poststreptococcal glomerulonephritis, systemic lupus erythematosus or Schönlein-Henoch syndrome, diffuse, selective mesangial IgA deposition was observed. Clinically, persistent microscopic haematuria,
J, Nagy +5 more
openaire +2 more sources
Renal biopsy specimens from 204 patients with glomerulonephritis or nephrotic syndrome have been studied. In ten of the patients not suffering from acute poststreptococcal glomerulonephritis, systemic lupus erythematosus or Schönlein-Henoch syndrome, diffuse, selective mesangial IgA deposition was observed. Clinically, persistent microscopic haematuria,
J, Nagy +5 more
openaire +2 more sources
IgA-Associated Glomerulonephritis
Annual Review of Medicine, 1977In summary, IgA-associated glomerulonephritis is an interesting clinical problem. The immunohistochemical identification of renal IgA deposits is the sine qua non of its diagnosis, although most of the patients reported have had hematuric syndromes, particularly recurrent gross hematuria. The importance of this immunopathologic entity devolves from the
openaire +2 more sources
IgA Glomerulonephritis in Japan
2015A clinicopathological study was done on 85 Japanese patients with IgA glomerulonephritis. Of patients with glomerulonephritis whose clinical course is of slow progression, the presence of IgA glomerulonephritis was demonstrated immunohistologically. The majority of such patients presented with a mild degree of proteinuria and/or persistent microscopic ...
Y, Ueda +4 more
openaire +2 more sources
Interstitial Myofibroblasts in IgA Glomerulonephritis
American Journal of Nephrology, 1995We examined renal biopsy specimens from patients with mesangial IgA glomerulonephritis (n = 25; plasma creatinine 0.05-0.30 mmol/l) to ascertain whether the myofibroblast has a role in progressive renal interstitial fibrosis. Myofibroblasts were identified by morphology and alpha smooth muscle actin (alpha-SMA) immunostaining at the light and electron ...
T D, Hewitson, G J, Becker
openaire +2 more sources
La Revue du praticien, 1992
Primary IgA nephritis is the most frequent nephritis and represent half of the glomerular diseases. Its incidence is 2,7/10(5) inhabitants. The diagnosis is established on a renal biopsy, which shows typical IgA mesangial deposits: granular, predominant, and diffuse. A central pathogenic role is played by the IgA immune system, both from the mucosa and
E, Alamartine, F, Berthoux
openaire +1 more source
Primary IgA nephritis is the most frequent nephritis and represent half of the glomerular diseases. Its incidence is 2,7/10(5) inhabitants. The diagnosis is established on a renal biopsy, which shows typical IgA mesangial deposits: granular, predominant, and diffuse. A central pathogenic role is played by the IgA immune system, both from the mucosa and
E, Alamartine, F, Berthoux
openaire +1 more source