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Items: 1 to 20 of 65


Self-assembled α-Tocopherol Transfer Protein Nanoparticles Promote Vitamin E Delivery Across an Endothelial Barrier.

Aeschimann W, Staats S, Kammer S, Olieric N, Jeckelmann JM, Fotiadis D, Netscher T, Rimbach G, Cascella M, Stocker A.

Sci Rep. 2017 Jul 10;7(1):4970. doi: 10.1038/s41598-017-05148-9.


Systematic review of autosomal recessive ataxias and proposal for a classification.

Beaudin M, Klein CJ, Rouleau GA, Dupré N.

Cerebellum Ataxias. 2017 Feb 23;4:3. doi: 10.1186/s40673-017-0061-y. eCollection 2017. Review.


Rice Bran Dietary Supplementation Improves Neurological Symptoms and Loss of Purkinje Cells in Vitamin E-Deficient Mice.

Takahashi T, Nakaso K, Horikoshi Y, Hanaki T, Yamakawa M, Nakasone M, Kitagawa Y, Koike T, Matsura T.

Yonago Acta Med. 2016 Sep 12;59(3):188-195. eCollection 2016 Sep.


More Than Ataxia: Hyperkinetic Movement Disorders in Childhood Autosomal Recessive Ataxia Syndromes.

Pearson TS.

Tremor Other Hyperkinet Mov (N Y). 2016 Jul 16;6:368. doi: 10.7916/D8H70FSS. eCollection 2016. Review.


Screening of α-Tocopherol Transfer Protein Sensitive Genes in Human Hepatoma Cells (HepG2).

Qu YH, Fu JC, Liu K, Zuo ZY, Jia HN, Ma Y, Luo HL.

Int J Mol Sci. 2016 Jun 27;17(7). pii: E1016. doi: 10.3390/ijms17071016.


Vitamin E and Phosphoinositides Regulate the Intracellular Localization of the Hepatic α-Tocopherol Transfer Protein.

Chung S, Ghelfi M, Atkinson J, Parker R, Qian J, Carlin C, Manor D.

J Biol Chem. 2016 Aug 12;291(33):17028-39. doi: 10.1074/jbc.M116.734210. Epub 2016 Jun 15.


Ataxia with Vitamin E Deficiency May Present with Cervical Dystonia.

Becker AE, Vargas W, Pearson TS.

Tremor Other Hyperkinet Mov (N Y). 2016 May 17;6:374. doi: 10.7916/D8B85820. eCollection 2016.


Dehydroepiandrosterone alters vitamin E status and prevents lipid peroxidation in vitamin E-deficient rats.

Miyazaki H, Takitani K, Koh M, Inoue A, Tamai H.

J Clin Biochem Nutr. 2016 May;58(3):223-31. doi: 10.3164/jcbn.15-133. Epub 2016 Apr 13.


A Case of Ataxia with Isolated Vitamin E Deficiency Initially Diagnosed as Friedreich's Ataxia.

Bonello M, Ray P.

Case Rep Neurol Med. 2016;2016:8342653. doi: 10.1155/2016/8342653. Epub 2016 Feb 16.


Complexity of vitamin E metabolism.

Schmölz L, Birringer M, Lorkowski S, Wallert M.

World J Biol Chem. 2016 Feb 26;7(1):14-43. doi: 10.4331/wjbc.v7.i1.14. Review.


Anti-inflammatory therapies of amyotrophic lateral sclerosis guided by immune pathways.

Lam L, Halder RC, Montoya DJ, Rubbi L, Rinaldi A, Sagong B, Weitzman S, Rubattino R, Singh RR, Pellegrini M, Fiala M.

Am J Neurodegener Dis. 2015 Dec 28;4(2):28-39. eCollection 2015.


Genes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2).

Guissart C, Drouot N, Oncel I, Leheup B, Gershoni-Barush R, Muller J, Ferdinandusse S, Larrieu L, Anheim M, Arslan EA, Claustres M, Tranchant C, Topaloglu H, Koenig M.

Eur J Hum Genet. 2016 Aug;24(8):1154-9. doi: 10.1038/ejhg.2015.259. Epub 2015 Dec 16.


Complete APTX deletion in a patient with ataxia with oculomotor apraxia type 1.

van Minkelen R, Guitart M, Escofet C, Yoon G, Elfferich P, Bolman GM, van der Helm R, van de Graaf R, van den Ouweland AM.

BMC Med Genet. 2015 Aug 19;16:61. doi: 10.1186/s12881-015-0213-y.


Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.

Hamza W, Ali Pacha L, Hamadouche T, Muller J, Drouot N, Ferrat F, Makri S, Chaouch M, Tazir M, Koenig M, Benhassine T.

BMC Med Genet. 2015 Jun 12;16:36. doi: 10.1186/s12881-015-0180-3.


Occupational therapy intervention to inspire self-efficacy in a patient with spinal ataxia and visual disturbance.

Tohyama S, Usuki F.

BMJ Case Rep. 2015 Feb 9;2015. pii: bcr2014208259. doi: 10.1136/bcr-2014-208259.


Effects of vitamin E on cognitive performance during ageing and in Alzheimer's disease.

La Fata G, Weber P, Mohajeri MH.

Nutrients. 2014 Nov 28;6(12):5453-72. doi: 10.3390/nu6125453. Review.



Akbar U, Ashizawa T.

Neurol Clin. 2015 Feb;33(1):225-48. doi: 10.1016/j.ncl.2014.09.004. Review.


Vitamin E is essential for Purkinje neuron integrity.

Ulatowski L, Parker R, Warrier G, Sultana R, Butterfield DA, Manor D.

Neuroscience. 2014 Feb 28;260:120-9. doi: 10.1016/j.neuroscience.2013.12.001. Epub 2013 Dec 14.


Identification of CHIP as a novel causative gene for autosomal recessive cerebellar ataxia.

Shi Y, Wang J, Li JD, Ren H, Guan W, He M, Yan W, Zhou Y, Hu Z, Zhang J, Xiao J, Su Z, Dai M, Wang J, Jiang H, Guo J, Zhou Y, Zhang F, Li N, Du J, Xu Q, Hu Y, Pan Q, Shen L, Wang G, Xia K, Zhang Z, Tang B.

PLoS One. 2013 Dec 2;8(12):e81884. doi: 10.1371/journal.pone.0081884. eCollection 2013.


Mechanisms for the prevention of vitamin E excess.

Traber MG.

J Lipid Res. 2013 Sep;54(9):2295-306. doi: 10.1194/jlr.R032946. Epub 2013 Mar 15. Review.

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