硫胺素转运蛋白基因突变与类韦尼克脑病 - Suppr

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Mutations in a thiamine-transporter gene and Wernicke's-like encephalopathy.

作者信息

Kono Satoshi, Miyajima Hiroaki, Yoshida Kenichi, Togawa Akashi, Shirakawa Kentaro, Suzuki Hitoshi

出版信息

N Engl J Med. 2009 Apr 23;360(17):1792-4. doi: 10.1056/NEJMc0809100.

DOI:10.1056/NEJMc0809100

PMID:19387023

Abstract

摘要

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相似文献

Mutations in a thiamine-transporter gene and Wernicke's-like encephalopathy.

N Engl J Med. 2009 Apr 23;360(17):1792-4. doi: 10.1056/NEJMc0809100.

[Familial Wernicke's-like encephalopathy].

Rinsho Shinkeigaku. 2010 Nov;50(11):855-7. doi: 10.5692/clinicalneurol.50.855.

[Reduced vision in Wernicke's syndrome with symptoms of nystagmus].

Ugeskr Laeger. 2006 Apr 3;168(14):1451-2.

Transient decrease of water diffusion in Wernicke's encephalopathy.

Neuroradiology. 2002 Apr;44(4):305-7. doi: 10.1007/s00234-001-0737-z. Epub 2002 Feb 16.

Full blown picture of Wernicke's encephalopathy.

QJM. 2010 Nov;103(11):891-2. doi: 10.1093/qjmed/hcp178. Epub 2009 Dec 7.

Wernicke's encephalopathy in a patient with multiple symmetrical lipomatosis and the A8344G mutation of mitochondrial DNA.

Eur Neurol. 2002;47(2):126-8. doi: 10.1159/000047967.

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Acta Ophthalmol. 2011 Dec;89(8):e656-7. doi: 10.1111/j.1755-3768.2010.02033.x. Epub 2010 Nov 23.

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Case Rep Neurol. 2024 Dec 3;17(1):1-8. doi: 10.1159/000542886. eCollection 2025 Jan-Dec.

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J Epilepsy Res. 2023 Dec 31;13(2):59-62. doi: 10.14581/jer.23010. eCollection 2023 Dec.

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Mol Genet Metab Rep. 2023 Aug 27;37:101004. doi: 10.1016/j.ymgmr.2023.101004. eCollection 2023 Dec.

Acute Encephalopathy Caused by Inherited Metabolic Diseases.

J Clin Med. 2023 May 31;12(11):3797. doi: 10.3390/jcm12113797.

Oxidative stress in Wernicke's encephalopathy.

Front Aging Neurosci. 2023 May 16;15:1150878. doi: 10.3389/fnagi.2023.1150878. eCollection 2023.