Hereditary tyrosinemia and tyrosyluria: clinical report of four patients.

Ítems similars

• The phenotypic manifestations of hereditary tyrosinemia and tyrosyluria: a hypothesis.
  per: Scriver, C. R.
  Publicat: (1967)
• Investigation in vivo of the Biochemical Defect in Hereditary Tyrosinemia and Tyrosyluria
  per: Scriver, C. R., et al.
  Publicat: (1967)
• Clinical and biochemical study of three patients with tyrosyluria.
  per: Sass-Kortsak, A., et al.
  Publicat: (1967)
• Observations on treatment in patients with tyrosyluria.
  per: Sass-Kortsak, A., et al.
  Publicat: (1967)
• Secondary metabolic derangements in patients with tyrosyluria.
  per: Sass-Kortsak, A., et al.
  Publicat: (1967)