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Results: 1 to 20 of 24

1.

Genome-wide screening of alpha-tocopherol sensitive genes in heart tissue from alpha-tocopherol transfer protein null mice (ATTP(-/-)).

Vasu VT, Hobson B, Gohil K, Cross CE.

FEBS Lett. 2007 Apr 17;581(8):1572-8. Epub 2007 Mar 15.

PMID:
17382327
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

A family with spinocerebellar ataxia type 8 expansion and vitamin E deficiency ataxia.

Cellini E, Piacentini S, Nacmias B, Forleo P, Tedde A, Bagnoli S, Ciantelli M, Sorbi S.

Arch Neurol. 2002 Dec;59(12):1952-3.

PMID:
12470185
[PubMed - indexed for MEDLINE]
3.

Increased atherosclerosis in hyperlipidemic mice deficient in alpha -tocopherol transfer protein and vitamin E.

Terasawa Y, Ladha Z, Leonard SW, Morrow JD, Newland D, Sanan D, Packer L, Traber MG, Farese RV Jr.

Proc Natl Acad Sci U S A. 2000 Dec 5;97(25):13830-4.

PMID:
11095717
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Familial ataxia with isolated vitamin E deficiency not due to mutation of alpha-TTP.

Shiojiri T, Yokota T, Fujimori N, Mizusawa H.

J Neurol. 1999 Oct;246(10):982. No abstract available.

PMID:
10552255
[PubMed - indexed for MEDLINE]
5.

Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency.

Schuelke M, Mayatepek E, Inter M, Becker M, Pfeiffer E, Speer A, Hübner C, Finckh B.

J Pediatr. 1999 Feb;134(2):240-4.

PMID:
9931538
[PubMed - indexed for MEDLINE]
6.

Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families.

Cavalier L, Ouahchi K, Kayden HJ, Di Donato S, Reutenauer L, Mandel JL, Koenig M.

Am J Hum Genet. 1998 Feb;62(2):301-10.

PMID:
9463307
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Retinitis pigmentosa and ataxia caused by a mutation in the gene for the alpha-tocopherol-transfer protein.

Yokota T, Shiojiri T, Gotoda T, Arai H.

N Engl J Med. 1996 Dec 5;335(23):1770-1. No abstract available.

PMID:
8965888
[PubMed - indexed for MEDLINE]
Free Article
8.

Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency.

Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed.

Ann Neurol. 1996 Mar;39(3):295-300.

PMID:
8602747
[PubMed - indexed for MEDLINE]
9.

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Ben Hamida C, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, et al.

Nat Genet. 1993 Oct;5(2):195-200.

PMID:
8252047
[PubMed - indexed for MEDLINE]
10.

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.

Ben Hamida M, Belal S, Sirugo G, Ben Hamida C, Panayides K, Ionannou P, Beckmann J, Mandel JL, Hentati F, Koenig M, et al.

Neurology. 1993 Nov;43(11):2179-83.

PMID:
8232925
[PubMed - indexed for MEDLINE]
11.

Human alpha-tocopherol transfer protein: cDNA cloning, expression and chromosomal localization.

Arita M, Sato Y, Miyata A, Tanabe T, Takahashi E, Kayden HJ, Arai H, Inoue K.

Biochem J. 1995 Mar 1;306 ( Pt 2):437-43.

PMID:
7887897
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.

Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M.

Nat Genet. 1995 Feb;9(2):141-5.

PMID:
7719340
[PubMed - indexed for MEDLINE]
13.

Adult-onset spinocerebellar dysfunction caused by a mutation in the gene for the alpha-tocopherol-transfer protein.

Gotoda T, Arita M, Arai H, Inoue K, Yokota T, Fukuo Y, Yazaki Y, Yamada N.

N Engl J Med. 1995 Nov 16;333(20):1313-8.

PMID:
7566022
[PubMed - indexed for MEDLINE]
Free Article
14.

Neuromyopathy and vitamin E deficiency in man.

Burck U, Goebel HH, Kuhlendahl HD, Meier C, Goebel KM.

Neuropediatrics. 1981 Aug;12(3):267-78.

PMID:
6945489
[PubMed - indexed for MEDLINE]
15.

A progressive neurological syndrome associated with an isolated vitamin E deficiency.

Laplante P, Vanasse M, Michaud J, Geoffroy G, Brochu P.

Can J Neurol Sci. 1984 Nov;11(4 Suppl):561-4.

PMID:
6509402
[PubMed - indexed for MEDLINE]
16.

The roles of vitamin E and unsaturated fatty acids in the visual process.

Robison WG, Kuwabara T, Bieri JG.

Retina. 1982;2(4):263-81. Review.

PMID:
6101134
[PubMed - indexed for MEDLINE]
17.

Neuromuscular disease in patients with steatorrhoea.

Binder HJ, Solitare GB, Spiro HM.

Gut. 1967 Dec;8(6):605-11. No abstract available.

PMID:
6079812
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Spinocerebellar degeneration associated with a selective defect of vitamin E absorption.

Harding AE, Matthews S, Jones S, Ellis CJ, Booth IW, Muller DP.

N Engl J Med. 1985 Jul 4;313(1):32-5. No abstract available.

PMID:
4000224
[PubMed - indexed for MEDLINE]
19.

Isolated deficiency of vitamin E with progressive neurologic deterioration.

Krendel DA, Gilchrist JM, Johnson AO, Bossen EH.

Neurology. 1987 Mar;37(3):538-40.

PMID:
3822155
[PubMed - indexed for MEDLINE]
20.

Adult-onset spinocerebellar syndrome with idiopathic vitamin E deficiency.

Yokota T, Wada Y, Furukawa T, Tsukagoshi H, Uchihara T, Watabiki S.

Ann Neurol. 1987 Jul;22(1):84-7.

PMID:
3477125
[PubMed - indexed for MEDLINE]

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