Kidney Biopsy Interpretation |
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Page 135
... Hereditary familial congenital hemorrhagic nephritis . Br . Med . J. 1 : 504-506 , 2. Antonovych , T. T. , et al .: Hereditary nephritis : Early clinical , functional , and morphological studies . Pediatr . Res . 3 : 545-556 , 1969 . 3 ...
... Hereditary familial congenital hemorrhagic nephritis . Br . Med . J. 1 : 504-506 , 2. Antonovych , T. T. , et al .: Hereditary nephritis : Early clinical , functional , and morphological studies . Pediatr . Res . 3 : 545-556 , 1969 . 3 ...
Page 279
... glomerulonephritis and , 59 Wegener's granulomatosis and , 200 DEAFNESS , hereditary nephritis and , 126 Dense deposit disease , 63 Deposits amyloid , 230 diabetic lesions vs. , 254 C component , systemic lupus erythematosus and , 154 ...
... glomerulonephritis and , 59 Wegener's granulomatosis and , 200 DEAFNESS , hereditary nephritis and , 126 Dense deposit disease , 63 Deposits amyloid , 230 diabetic lesions vs. , 254 C component , systemic lupus erythematosus and , 154 ...
Page 281
... Hereditary interstitial pyelonephritis , 125 Nephrotic syndrome ( s ) , 13–88 . See also. Glomerulonephritis - Continued polyarteritis nodosa vs. , 190 perimembranous , 34. See also Membranous neph- ropathy . postinfectious , acute ...
... Hereditary interstitial pyelonephritis , 125 Nephrotic syndrome ( s ) , 13–88 . See also. Glomerulonephritis - Continued polyarteritis nodosa vs. , 190 perimembranous , 34. See also Membranous neph- ropathy . postinfectious , acute ...
Contents
Introduction | 1 |
Primary Glomerular Diseases | 13 |
Hematuria Syndromes | 89 |
Copyright | |
9 other sections not shown
Common terms and phrases
acute adults affected amyloid amyloidosis and/or antibodies appear Arch associated basement membrane capillary loops cent changes Chap childhood chronic Clin clinical complement complex component congenital contain correlations course crescents cytoplasm deposits develop diabetic diagnosis diffuse disease early electron microscopy electron-dense deposits endothelial epithelial cells et al extensive familial FIGURE findings focal glomerular capillary glomeruli glomerulonephritis glomerulosclerosis granular H&E stain hematuria hereditary hyaline hypertension immune immunofluorescent immunoglobulin incidence increase infection Intern interstitial Invest Kidney Kidney Int lamina Lancet lesions light microscopy lupus nephritis matrix membranous nephropathy mesangial cells mild nephrotic syndrome normal occasionally occur onset pathogenesis Pathol patients pattern Pediatr persistent PRECEDING present primary produces prognosis progressive proliferation prominent proteinuria PSGN pyuria recurrent renal biopsy renal disease renal involvement reported sclerosis seen segmental serum severity significant silver subendothelial subepithelial systemic lupus erythematosus therapy thickening tion transplantation treatment tubular typically variable vascular