SYNGAP1 encephalopathy A distinctive generalized developmental and epileptic encephalopathy (vol 92, pg e96, 2019)

Vlaskamp

首页> 外文期刊>Neurology. >SYNGAP1 encephalopathy A distinctive generalized developmental and epileptic encephalopathy (vol 92, pg e96, 2019)

【24h】

SYNGAP1 encephalopathy A distinctive generalized developmental and epileptic encephalopathy (vol 92, pg e96, 2019)

机译：独特的广义SYNGAP1脑病发展和癫痫性脑病(卷92年,pg e96, 2019)

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Neurology.》 |2019年第20期|908-908|共1页
作者
Vlaskamp;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种英语
中图分类
关键词
SYNGAP1 gene; Epilepsy; Encephalopathy;

机译：SYNGAP1基因、癫痫、脑病;

相似文献

外文文献
中文文献

1. Epileptic Encephalopathies in Infants and Children: Study of Clinico-Electroencephalographic Spectrum in a Tertiary Hospital in Bangladesh [J] . Bithi Debnath, Rajib Nayan Chowdhury, Narayan Chandra Shaha, 儿科学期刊（英文） . 2021,第003期
2. Regeneration of neurotransmission transcriptome in a model of epileptic encephalopathy after antiinflammatory treatment [J] . Dumitru A. Iacobaş, Libor Velíšek 中国神经再生研究（英文版） . 2018,第10期
3. Correlation of brain cell glucose metabolism and patient's condition in children with epileptic encephalopathy An assessment using fluorine-18-fluoro-2-deoxy-D-glucose positron emission computed tomography [J] . Qiongxiang Zhai, Yuxiong Guo, Yuxin Zhang, 中国神经再生研究（英文版） . 2011,第32期
4. Changes in hippocampal neurons and memory function during the developmental stage of newborn rats with hypoxic-ischemic encephalopathy [J] . Chuanjun Liu, Yue Li, Huiying Gao 中国神经再生研究（英文版） . 2006,第8期
5. Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum. [J] . Renzo Guerrini, Valerio Conti, Massimo MantegazzaSimona BalestriniAristea S GalanopoulouFabio Benfenati Physiological Reviews . 2023,第1期

机译：Developmental and epileptic encephalopathies: from genetic heterogeneity to phenotypic continuum.
6. A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a [J] . Harms Frederike L., Weiss Deike, Lisfeld JasminAlawi MalikKutsche Kerstin Neurogenetics . 2023,第3期

机译：A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a
7. Figure 92 from: Albano PG, Bakker PAJ, Sabelli B (2019) Annotated catalogue of the types of Triphoridae (Mollusca, Gastropoda) in the Natural History Museum of the United Kingdom, London. Zoosystematics and Evolution 95(1): 161-308. https://doi.org/10.3897/zse.95.32803 [O] . Paolo G. Albano, Piet A. J. Bakker, Bruno Sabelli 2019

机译：图92来自：Albano PG，Bakker PAJ，Sabelli B（2019）伦敦自然历史博物馆的Triphoridae（Mollusca，Gastropoda）类型的批发目录。 Zoosystematics和Evolution 95（1）：161-308。 https://doi.org/10.3897/zse.95.32803

SYNGAP1 encephalopathy A distinctive generalized developmental and epileptic encephalopathy (vol 92, pg e96, 2019)

著录项

相似文献

相关主题

期刊订阅