Urinary 3-hydroxyproline excretion in Alport's syndrome: a non-invasive screening test?

Author:

Bartosch B,Vycudilik W,Popow C,Lubec G

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Characteristic ultrastructural lesions of the glomerular basement membrane in progressive hereditary glomerulonephritis (Alport's syndrome);Hinglais, N.; Grunfeld, J.P.; Bois, E.;Lab Invest,1972

2. Definition of the glomerular basement membrane;Lubec, G.;Renal Physiol,1983

3. Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis;McCoy, R.C.; Johnson, H.K.; Stone, W.H.; Wislon, C.S.;Kidney Int,1982

4. Noninvasive diagnosis of Alport's syndrome;Lubec, G.; Chamdawallah, S.;Lancet,1984

5. Alport's syndrome: a genetic defect in biochemical composition of basement membranes of glomerulus, lens and inner ear?;GF, Di Bona;Laboratory and Clinical Medicine,1983

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