Split and extremely thin glomerular basement membranes in hereditary nephropathy (Alport's syndrome).

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作者信息

Rumpelt H J, Langer K H, Schärer K, Straub E, Thoenes W

出版信息

Virchows Arch A Pathol Anat Histol. 1974;364(3):225-33. doi: 10.1007/BF00433075.

DOI:10.1007/BF00433075

PMID:4219460

Abstract

摘要

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IDIOPATHIC NEPHROTIC SYNDROME IN ADULTS. A STUDY AND CLASSIFICATION BASED ON RENAL BIOPSIES.

N Engl J Med. 1965 Jan 28;272:165-74. doi: 10.1056/NEJM196501282720401.

Anatomy of the glomerulus as observed in biopsy material from young and healthy human subjects.

Z Zellforsch Mikrosk Anat. 1958;48(1):51-73. doi: 10.1007/BF00496712.

An electron microscope study of the glomerulus in nephrosis, glomerulonephritis, and lupus erythematosus.

J Exp Med. 1957 Nov 1;106(5):649-60. doi: 10.1084/jem.106.5.649.

Studies on familial nephrosis. II. Glomerular changes observed with the electron microscope.

Am J Pathol. 1957 Jul-Aug;33(4):791-817.

Hereditary renal disease associated with deafness--Alport's syndrome.

Acta Med Scand. 1966 Mar;179(3):319-28. doi: 10.1111/j.0954-6820.1966.tb05464.x.

Thickness of glomerular basement membranes.

Am J Clin Pathol. 1966 Jan;45(1):7-20. doi: 10.1093/ajcp/45.1.7.

The ultastructure of the normal human glomerulus. Thickness of glomerular basement membrane.

Lab Invest. 1968 Jan;18(1):42-8.

Hereditary chronic nephritis (alport) complicated by nephrotic syndrome. Light, Fluorescent and electronmicroscopic studies of renal biopsy specimens.

Acta Med Biol (Niigata). 1969 Sep;17(2):101-17.

[Electron microscopical findings in the kidneys in Alport's syndrome].

Frankf Z Pathol. 1966;76(1):12-20.

Diffuse familial nephropathy: a clinicopathological study.

J Pediatr. 1970 Jul;77(1):37-47. doi: 10.1016/s0022-3476(70)80042-7.

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