Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation

Bhoi Sanjeev K.; Naik Suprava; Dubey Deepanshu; Kalita Jayantee; Misra Usha Kant

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Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation

机译：Moyamoya综合征在甲基四氢溶酯还原酶突变的孩子中

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来源
《Neurology India.》 |2017年第6期|共2页
作者
Bhoi Sanjeev K.; Naik Suprava; Dubey Deepanshu; Kalita Jayantee; Misra Usha Kant;
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作者单位

All India Inst Med Sci Dept Neurol Bhubaneswar Odisha India;

All India Inst Med Sci Dept Radiodiag Bhubaneswar Odisha India;

Sanjay Gandhi Postgrad Inst Med Sci Dept Neurol Lucknow 226014 Uttar Pradesh India;

Sanjay Gandhi Postgrad Inst Med Sci Dept Neurol Lucknow 226014 Uttar Pradesh India;

Sanjay Gandhi Postgrad Inst Med Sci Dept Neurol Lucknow 226014 Uttar Pradesh India;

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原文格式 PDF
正文语种 eng
中图分类神经病学与精神病学;
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1. Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation [J] . Bhoi Sanjeev K., Naik Suprava, Dubey Deepanshu, Neurology India. . 2017,第6期

机译：Moyamoya综合征在甲基四氢溶酯还原酶突变的孩子中
2. Comparative Study between the Use of Regular Folic Acid Supplement versus the Use of L-Methyl Folate in Patients with Methyl Tetrahydrofolate Reductase (MTHFR) Gene Mutation with Recurrent Pregnancy Loss [J] . Ahmed Essmat 妇产科期刊（英文） . 2021,第009期

机译：Comparative Study between the Use of Regular Folic Acid Supplement versus the Use of L-Methyl Folate in Patients with Methyl Tetrahydrofolate Reductase (MTHFR) Gene Mutation with Recurrent Pregnancy Loss
3. Sneddon Syndrome with Factor V Leiden, Methylene Tetrahydrofolate Reductase and FMF Gene Mutations [J] . Murat Terzi, Duran Yaz?c?, Emine Sabanc?lar, Turk Neuroloji Dergisi . 2010,第1期

机译：具有因子V Leiden，亚甲基四氢叶酸还原酶和FMF基因突变的Sneddon综合征
4. Ungiographic Findings in European Moyamoya Disease and Moyamoya Syndrome [C] . N.Khan, B. Schuknecht, HG. Imhof, European Congress of Neurosurgery . 2003

机译：欧洲Moyamoya病和Moyamoya综合征的血管造影结果
5. Effects of Genetic Susceptibility and Psychosocial Stressors on Executive Functioning in Mothers With the Fragile X Premutation Who Have a Child With Fragile X Syndrome [D] . Carns, Danielle Renee. 2019

机译：遗传易感性和心理社会压力对母亲雌性X综合征患儿的母亲X综合征
6. Acute portal vein thrombosis secondary to hyperhomocysteinemia with folic acid deficiency and methyl tetrahydrofolate reductase mutation: a case report and literature review [O] . Yosra Messaoudi, Mohamed Hedfi, Najeh Benhalima, 2016

机译：高同型半胱氨酸血症伴叶酸缺乏和四氢叶酸甲酯还原酶突变引起的急性门静脉血栓形成：一例病例并文献复习
7. Mutations in the methylene-tetrahydrofolate reductase gene and Down syndrome [O] . Grillo, Laura Brunelli das Neves, Acácio, Gregório Lorenzo, Barini, Ricardo, 2015

机译：亚甲基四氢叶酸还原酶基因突变和唐氏综合症

Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation

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