Osteopetrosis, acidosis tubular renal, calcificaciones cerebrales: caso familiar

Lignende værker

• Carbonic anhydrase II deficiency identified as the primary defect in the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.
  af: Sly, W S, et al.
  Udgivet: (1983)
• Correction of renal tubular acidosis in carbonic anhydrase II-deficient mice with gene therapy.
  af: Lai, L W, et al.
  Udgivet: (1998)
• Osteopetrosis, acidosis tubular renal, calcificaciones cerebrales: caso familiar
  af: Saturnino Ortiz Madinaveitia, et al.
  Udgivet: (2019-10-01)
• Inactive form of erythrocyte carbonic anhydrase B in patients with primary renal tubular acidosis.
  af: Kondo, T, et al.
  Udgivet: (1978)
• Carbonic Anhydrase II Activators in Osteopetrosis Treatment: A Review
  af: Zikra Alkhayal, et al.
  Udgivet: (2023-02-01)