Fragmentation of filtered proteins and implications for glomerular protein sieving in Fanconi syndrome.

Samankaltaisia teoksia

• Glomerular protein sieving and implications for renal failure in Fanconi syndrome.
  Tekijä: Norden, A, et al.
  Julkaistu: (2001)
• Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome.
  Tekijä: Norden, A, et al.
  Julkaistu: (2002)
• Tubular proteinuria defined by a study of Dent's (CLCN5 mutation) and other tubular diseases.
  Tekijä: Norden, A, et al.
  Julkaistu: (2000)
• THE GENE CAUSING DENTS DISEASE, A RENAL FANCONI SYNDROME WITH NEPHROCALCINOSIS AND KIDNEY-STONES, IS ON THE SHORT ARM OF THE X-CHROMOSOME (XP11.22)
  Tekijä: Thakker, R, et al.
  Julkaistu: (1993)
• Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22.
  Tekijä: Pook, M, et al.
  Julkaistu: (1993)