Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset [3]

Journal of Neurology Neurosurgery and Psychiatry

Volumn 60, Issue 1, 1996, Pages 107-108

  Gold, R ^a   Bogdahn, U ^a   Kappos, L ^a   Toyka, K V ^a   Regula Baumgartner, E ^a   Fowler, B ^a   Wendel, U ^a  

^a UNIVERSITY HOSPITAL WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN; COBAMAMIDE; HYDROXOCOBALAMIN; MECOBALAMIN; METHIONINE SYNTHASE; METHYLMALONYL COENZYME A MUTASE;

ADULT; CASE REPORT; FEMALE; GAS CHROMATOGRAPHY; HOMOCYSTINURIA; HUMAN; LETTER; MASS SPECTROMETRY; METABOLIC DISORDER; METHYLMALONIC ACIDURIA; NERVE BIOPSY; NEUROPATHY; ONSET AGE; PRIORITY JOURNAL; SKIN FIBROBLAST; SPINAL CORD DISEASE; SURAL NERVE; VITAMIN METABOLISM;

EID: 0030061817     PISSN: 00223050     EISSN: None     Source Type: Journal    
DOI: 10.1136/jnnp.60.1.107     Document Type: Letter

References (0)