• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利：CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法，用中文像聊天一样搜索，搜遍4000万医学文献。AI智能推荐，让科研检索更轻松。

立即免费搜索

文件翻译

保留排版，准确专业，支持PDF/Word/PPT等文件格式，支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述，25分钟生成高质量综述，智能提取关键信息，辅助科研写作。

立即免费体验

Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder.

作者信息

Padmanabha Hansashree, Shekhar Ravi, Mahale Rohan, Annam Harikrishna, Bhat Maya, Sangeeth Thuppanattumadam A, Christopher Rita, Arunachal Gautham, Mailankody Pooja, Mathuranath Pavagada S

机构信息

Department of Neurology, Neuroscience Faculty Center, National Institute of Mental Health and Neurosciences, Bengaluru, India.

Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences, Bengaluru, India.

出版信息

J Inherit Metab Dis. 2021 Nov;44(6):1505-1506. doi: 10.1002/jimd.12439. Epub 2021 Sep 28.

DOI:10.1002/jimd.12439
PMID:34541688
Abstract
摘要

相似文献

1
Reversible leukoencephalopathy and cerebral atrophy in homocystinuria due to MTHFR deficiency: A treatable metabolic disorder.因亚甲基四氢叶酸还原酶（MTHFR）缺乏导致的同型胱氨酸尿症中的可逆性白质脑病和脑萎缩：一种可治疗的代谢紊乱疾病。
J Inherit Metab Dis. 2021 Nov;44(6):1505-1506. doi: 10.1002/jimd.12439. Epub 2021 Sep 28.
2
Focal epilepsy as the revealing symptom of 5,10-methylenetetrahydrofolate reductase deficiency in a young adult.局灶性癫痫作为一名年轻成人5,10-亚甲基四氢叶酸还原酶缺乏症的首发症状
Rev Neurol (Paris). 2018 Mar;174(3):173-175. doi: 10.1016/j.neurol.2017.06.028. Epub 2018 Feb 1.
3
[Posterior-predominant leukoencephalopathy which was caused by methylenetetrahydrofolate reductase deficiency and successfully treated with folic acid].[由亚甲基四氢叶酸还原酶缺乏引起的以后部为主的白质脑病并成功用叶酸治疗]
Rinsho Shinkeigaku. 2014;54(3):200-6. doi: 10.5692/clinicalneurol.54.200.
4
Acute leukoencephalopathy possibly induced by phenytoin intoxication in an adult patient with methylenetetrahydrofolate reductase deficiency.急性白细胞脑病可能由亚叶酸还原酶缺乏症成年患者的苯妥英钠中毒引起。
Epilepsia. 2011 Jul;52(7):e58-61. doi: 10.1111/j.1528-1167.2011.03064.x. Epub 2011 Apr 11.
5
[Methylenetetrahydrofolate reductase deficiency-induced schizophrenia in a school-age boy].[亚甲基四氢叶酸还原酶缺乏症致一名学龄期男孩患精神分裂症]
Zhongguo Dang Dai Er Ke Za Zhi. 2014 Jan;16(1):62-6.
6
Severe 5,10-methylenetetrahydrofolate reductase deficiency: a rare, treatable cause of complicated hereditary spastic paraplegia.严重的 5,10-亚甲基四氢叶酸还原酶缺乏症：一种罕见的、可治疗的遗传性痉挛性截瘫复杂病因。
Eur J Neurol. 2018 Mar;25(3):602-605. doi: 10.1111/ene.13557. Epub 2018 Jan 30.
7
Methylenetetrahydrofolate Reductase Deficiency as a Cause of Treatable Adult-onset Leukoencephalopathy and Myelopathy.亚甲基四氢叶酸还原酶缺乏症作为成人起病的可治疗性白质脑病和脊髓病的病因
Clin Neuroradiol. 2021 Mar;31(1):277-281. doi: 10.1007/s00062-020-00947-6. Epub 2020 Sep 3.
8
Homocysteinemia due to MTHFR deficiency in a young adult presenting with bilateral lens subluxations.一名患有双侧晶状体半脱位的年轻成人因亚甲基四氢叶酸还原酶（MTHFR）缺乏导致高同型半胱氨酸血症。
Ophthalmic Genet. 2017 Jan-Feb;38(1):91-94. doi: 10.3109/13816810.2016.1143017. Epub 2016 Apr 4.
9
Early treatment using betaine and methionine for a neonate with MTHFR deficiency.对一名患有亚甲基四氢叶酸还原酶（MTHFR）缺乏症的新生儿早期使用甜菜碱和蛋氨酸进行治疗。
Pediatr Int. 2019 Dec;61(12):1265-1266. doi: 10.1111/ped.14018. Epub 2019 Nov 28.
10
[Methylenetetrahydrofolate Reductase deficiency and anesthesia: importance of a detailed preoperative evaluation].[亚甲基四氢叶酸还原酶缺乏与麻醉：详细术前评估的重要性]
Braz J Anesthesiol. 2019 Nov-Dec;69(6):637-638. doi: 10.1016/j.bjan.2019.05.002. Epub 2019 Nov 30.

引用本文的文献

1
White matter lesions contribute to motor and non-motor disorders in Parkinson's disease: a critical review.白质病变在帕金森病中导致运动和非运动障碍：一项批判性综述。
Geroscience. 2025 Feb;47(1):591-609. doi: 10.1007/s11357-024-01428-1. Epub 2024 Nov 22.