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Items: 14

1.

Vitamin-responsive disorders: cobalamin, folate, biotin, vitamins B1 and E.

Baumgartner MR.

Handb Clin Neurol. 2013;113:1799-810. doi: 10.1016/B978-0-444-59565-2.00049-6. Review.

PMID:
23622402
2.

Ataxia with vitamin E deficiency: update of molecular diagnosis.

Di Donato I, Bianchi S, Federico A.

Neurol Sci. 2010 Aug;31(4):511-5. doi: 10.1007/s10072-010-0261-1. Epub 2010 May 13. Review.

PMID:
20464573
3.

Ataxia with vitamin E deficiency in southeast Norway, case report.

Koht J, Bjørnarå KA, Jørum E, Tallaksen CM.

Acta Neurol Scand Suppl. 2009;(189):42-5. doi: 10.1111/j.1600-0404.2009.01214.x.

PMID:
19566498
4.

Ataxia with vitamin E deficiency (AVED); an example of the contribution of research in molecular genetic to counselling in Morocco.

Bellayou H, Dehbi H, Bourezgui M, Slassi I, Nadifi S.

Pathol Biol (Paris). 2009 Jul;57(5):425-6. doi: 10.1016/j.patbio.2008.09.014. Epub 2008 Nov 26. No abstract available.

PMID:
19038506
5.

Drug Insight: antioxidant therapy in inherited ataxias.

Pandolfo M.

Nat Clin Pract Neurol. 2008 Feb;4(2):86-96. doi: 10.1038/ncpneuro0704. Review.

PMID:
18256680
6.

Vitamin E deficiency ataxia with (744 del A) mutation on alpha-TTP gene: genetic and clinical peculiarities in Moroccan patients.

Marzouki N, Benomar A, Yahyaoui M, Birouk N, Elouazzani M, Chkili T, Benlemlih M.

Eur J Med Genet. 2005 Jan-Mar;48(1):21-8. Epub 2005 Feb 19.

PMID:
15953402
7.

Ataxia with isolated vitamin E deficiency: neurological phenotype, clinical follow-up and novel mutations in TTPA gene in Italian families.

Mariotti C, Gellera C, Rimoldi M, Mineri R, Uziel G, Zorzi G, Pareyson D, Piccolo G, Gambi D, Piacentini S, Squitieri F, Capra R, Castellotti B, Di Donato S.

Neurol Sci. 2004 Jul;25(3):130-7.

PMID:
15300460
8.

Friedreich's Ataxia: disease mechanisms, antioxidant and Coenzyme Q10 therapy.

Cooper JM, Schapira AH.

Biofactors. 2003;18(1-4):163-71. Review.

PMID:
14695932
9.

Ataxia with vitamin E deficiency and severe dystonia: report of a case.

Roubertie A, Biolsi B, Rivier F, Humbertclaude V, Cheminal R, Echenne B.

Brain Dev. 2003 Sep;25(6):442-5.

PMID:
12907280
10.

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.

Gabsi S, Gouider-Khouja N, Belal S, Fki M, Kefi M, Turki I, Ben Hamida M, Kayden H, Mebazaa R, Hentati F.

Eur J Neurol. 2001 Sep;8(5):477-81.

PMID:
11554913
11.

Ataxia with vitamin E deficiency: biochemical effects of malcompliance with vitamin E therapy.

Schuelke M, Finckh B, Sistermans EA, Ausems MG, Hübner C, von Moers A.

Neurology. 2000 Nov 28;55(10):1584-6.

PMID:
11094124
12.

Ataxia caused by mutations in the alpha-tocopherol transfer protein gene.

Usuki F, Maruyama K.

J Neurol Neurosurg Psychiatry. 2000 Aug;69(2):254-6.

13.

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F.

Neurology. 2000 Apr 11;54(7):1408-14.

PMID:
10751248
14.

Vitamin E updated.

Matthai J.

Indian J Pediatr. 1996 Mar-Apr;63(2):242-53. Review.

PMID:
10829996

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