Signs and symptoms of thin basement membrane nephropathy: A prospective regional study on primary glomerular disease—The Limburg Renal Registry

This publication has 11 references indexed in Scilit:

• A comparison of the clinical, histopathologic, and ultrastructural phenotypes in carriers of X-linked and autosomal recessive Alport's syndrome
  American Journal of Kidney Diseases, 2001
• COL4A4 mutation in thin basement membrane disease previously described in Alport syndrome11See Editorial by Monnens, p. 799
  Kidney International, 2001
• Clinical picture and outcome of primary focal segmental glomerulosclerosis.
  Nephrology Dialysis Transplantation, 1999
• Thin Glomerular Basement Membrane Nephropathy in Adults
  Nephron, 1998
• Preliminary technical report. Epitope-defined monoclonal antibodies against type-IV collagen for diagnosis of Alport's syndrome
  Nephrology Dialysis Transplantation, 1997
• Thin GBM nephropathy: Premature glomerular obsolescence is associated with hypertension and late onset renal failure
  Kidney International, 1997
• Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.
  Journal of Clinical Investigation, 1996
• The many masks of focal segmental glomerulosclerosis
  Kidney International, 1994
• Thin-Basement-Membrane Nephropathy in Adults with Persistent Hematuria
  New England Journal of Medicine, 1989
• Epidemiology of idiopathic glomerular disease: A prospective study
  Kidney International, 1987