Subacute combined degeneration of the spinal cord in cblC disorder despite treatment with B12
- 30 June 2006
- journal article
- case report
- Published by Elsevier BV in Molecular Genetics and Metabolism
- Vol. 88 (2), 138-145
- https://doi.org/10.1016/j.ymgme.2006.02.007
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC typeNature Genetics, 2005
- Disorders of intermediary metabolism: Toxic leukoencephalopathiesJournal of Inherited Metabolic Disease, 2005
- Creatine metabolism in combined methylmalonic aciduria and homocystinuriaAnnals of Neurology, 2005
- Influence of vitamin B12 on brain methionine adenosyltransferase activity in senile dementia of the Alzheimer's typeJournal of Neural Transmission, 1996
- Methionine adenosyltransferase: Structure and functionPharmacology & Therapeutics, 1993
- Biochemical pathogenesis of subacute combined degeneration of the spinal cord and brainJournal of Inherited Metabolic Disease, 1993
- Hereditary Defect of Cobalamin Metabolism (CblGMutation) Presenting as a Neurologic Disorder in AdulthoodThe New England Journal of Medicine, 1988
- Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuriaThe Journal of Pediatrics, 1988
- Abnormal cobalamin metabolism in a megaloblastic child with homocystinuria, cystathioninuria and methylmalonic aciduriaJournal of Inherited Metabolic Disease, 1983
- A derangement in B12 metabolism leading to homocystinemia, cystathioninemia and methylmalonic aciduriaBiochemical and Biophysical Research Communications, 1969