Osteopetrosis, acidosis tubular renal, calcificaciones cerebrales: caso familiar

Geahča maid

• Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
  Dahkki: Sly, W S, et al.
  Almmustuhtton: (1983)
• Osteopetrosis, acidosis tubular renal, calcificaciones cerebrales: caso familiar
  Dahkki: Saturnino Ortiz Madinaveitia, et al.
  Almmustuhtton: (2019-10-01)
• Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.
  Dahkki: Kondo, T, et al.
  Almmustuhtton: (1978)
• Carbonic Anhydrase II Activators in Osteopetrosis Treatment: A Review
  Dahkki: Zikra Alkhayal, et al.
  Almmustuhtton: (2023-02-01)
• Enzymatically Inactive Red Cell Carbonic Anhydrase B in a Family with Renal Tubular Acidosis
  Dahkki: Shapira, Emmanuel, et al.
  Almmustuhtton: (1974)