Treatment of ataxia in isolated vitamin E deficiency caused by α-tocopherol transfer protein deficiency
- 1 February 1999
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 134 (2), 240-244
- https://doi.org/10.1016/s0022-3476(99)70424-5
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Human α‐tocopherol transfer protein: Gene structure and mutations in familial vitamin E deficiencyAnnals of Neurology, 1996
- Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer proteinNature Genetics, 1995
- Impaired degradation of leukotrienes in patients with peroxisome deficiency disorders.JCI Insight, 1993
- The relative contributions of vitamin E, urate, ascorbate and proteins to the total peroxyl radical-trapping antioxidant activity of human blood plasmaBiochimica et Biophysica Acta (BBA) - General Subjects, 1987
- Maturation of Central Somatosensory Conduction Time in Infancy and ChildhoodNeuropediatrics, 1986
- Improved Neurologic Function after Long-Term Correction of Vitamin E Deficiency in Children with Chronic CholestasisThe New England Journal of Medicine, 1985
- Inhibition of 5‐lipoxygenase by vitamin EFEBS Letters, 1985
- Spinocerebellar Degeneration Associated with a Selective Defect of Vitamin E AbsorptionThe New England Journal of Medicine, 1985
- VITAMIN E AND NEUROLOGICAL FUNCTIONThe Lancet, 1983
- NEUROMYOPATHY AND VITAMIN E DEFICIENCY in MAN1Neuropediatrics, 1981