Familial Isolated Vitamin E Deficiency
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-319-66816-1_1741-1
Reference9 articles.
1. Di Donato I, Bianchi S, Federico A (2010) Ataxia with vitamin E deficiency: update of molecular diagnosis. Neurol Sci 31:511–515. https://doi.org/10.1007/s10072-010-0261-1
2. El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F (2014) Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency. Brain 137:402–410. https://doi.org/10.1093/brain/awt339
3. Federico A (2004) Ataxia with isolated vitamin E deficiency: a treatable neurologic disorder resembling Friedreich’s ataxia. Neurol Sci 25:119–121. https://doi.org/10.1007/s10072-004-0245-0
4. Gana S, Valente EM (2020) Movement disorders in genetic pediatric ataxias. Mov Disord Clin Pract 7:383–393. https://doi.org/10.1002/mdc3.12937
5. Harding AE, Matthews S, Jones S, Ellis CJ, Booth IW, Muller DP (1985) Spinocerebellar degeneration associated with a selective defect of vitamin E absorption. N Engl J Med 313:32–35. https://doi.org/10.1056/NEJM198507043130107
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