Results 161 to 170 of about 21,381 (225)

Gelsolin amyloidosis presenting with nephrotic syndrome: a case report and molecular insights. [PDF]

Front Med (Lausanne)
Xiang S, Bi P, Chen D, Tang W, Li Y, Zhou Y, Kang D, Pan C, Wan F, Yu J, Tang X.   +10 more
europepmc   +1 more source

Response to the Letter to the Editor Entitled "Interleukin-18: A Critical Culprit in Inflammatory Renal Disease". [PDF]

Kidney Int Rep
Barbir EB, Ghimire A, Stokowski T, Thennakoonwela P, Brassington R, Churngchow W, Nasr SH, Gowrishankar M, Hildebrand A, Solez K.   +9 more
europepmc   +1 more source

The Influence of PAR 1 and Endothelin 1 on the Course of Specific Kidney Diseases. [PDF]

J Clin Med
Szymczak M, Żabińska M, Kościelska-Kasprzak K, Bartoszek D, Heidecke H, Schulze-Forster K, Janek Ł, Kujawa K, Wronowicz J, Marek-Bukowiec K, Gołębiowski T, Banasik M.   +11 more
europepmc   +1 more source

Rapid Remission of Steroid-Refractory IgA Nephropathy With Targeted-Release Budesonide: A Case Report. [PDF]

Cureus
Manrique-Pizarro PA, Cordero E.
europepmc   +1 more source

[The course and outcome of IgA glomerulonephritis].

Terapevticheskii arkhiv, 1997
V I, Naumova, Z M, Mikhaĭlova, E L, Panchenko, V P, Bobkova, Z B, Ketebaeva, O V, Chumakova   +5 more
openaire   +1 more source

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IgA‐Associated Glomerulonephritis

Australian and New Zealand Journal of Medicine, 1975
Summary: 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, N M, Thomson, R, Meadows, J R, Lawrence   +3 more
openaire   +2 more sources

IgA Glomerulonephritis in Japan

2015
A 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, O, Sakai, M, Yamagata, T, Kitajima, K, Kawamura   +4 more
openaire   +2 more sources

Interstitial Myofibroblasts in IgA Glomerulonephritis

American Journal of Nephrology, 1995
We 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