Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset.

Documenti analoghi

• Early-onset Combined Methylmalonic Aciduria and Homocystinuria: Neuroradiologic Findings
  di: Rossi, Andrea, et al.
  Pubblicazione: (2001)
• Disorder of intracellular cobalamin metabolism: Importance of rapid diagnostic illustrated by a case report of early-onset methylmalonic aciduria and homocystinuria, cobalamin C type
  di: Etienne Mondesert, et al.
  Pubblicazione: (2025-02-01)
• The value of neuroimaging in the assessment and follow-up of early-onset methylmalonic aciduria and homocystinuria()
  di: de Benedictis, Fernando M., et al.
  Pubblicazione: (2014)
• Prospective evaluation of pregnancy outcome in an Italian woman with late-onset combined homocystinuria and methylmalonic aciduria
  di: Grandone, Elvira, et al.
  Pubblicazione: (2019)
• The Value of 1H-MRS and MRI in Combined Methylmalonic Aciduria and Homocystinuria
  di: Cheng, Ailan, et al.
  Pubblicazione: (2019)