临床遗传学与rett综合征进化的相关方面

M. Marx, Tatiana de Menezes, H. M. T. Batista, Luiz Arthur Bevilaqua Bandeira, Antonio Marlos Duarte de Melo, G. Oliveira
{"title":"临床遗传学与rett综合征进化的相关方面","authors":"M. Marx, Tatiana de Menezes, H. M. T. Batista, Luiz Arthur Bevilaqua Bandeira, Antonio Marlos Duarte de Melo, G. Oliveira","doi":"10.14295/AIMJ.V2I4.39","DOIUrl":null,"url":null,"abstract":"Rett syndrome has yielded many articles over the years since its discovery. This is a production that aims to recover some concepts already brought by other authors, to fix the genetic aspect of the affection, as well as the clinical evolution and associated diseases. Methodology: The screen study is the result of consultations in national and international databases, most notably PubMed and Scielo as a source of academic articles. In the consultations we used the following keywords: Rett Syndrome, Mental Deficit, Multiple Deficit, Epileptic Crisis, and Genetics, we still serve three journals: Genomics & Genetics Weekly, Genetic, Social and General Psychology Monographs and Journal of Medical Genetics of the English equivalent as descriptors: Rett Syndrome, Mental Limitation, General Limitation, Epilepsy and Genetics. In our consultation we found 185 articles and of these, we use 32 to compose our bibliographic reference.  Keywords: Rett syndrome. Mental deficiency. Multiple Deficit. Epileptic","PeriodicalId":315563,"journal":{"name":"Amadeus International Multidisciplinary Journal","volume":"98 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-07-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"RELATED ASPECTS OF CLINICAL GENETICS AND RETT SYNDROME EVOLUTION\",\"authors\":\"M. Marx, Tatiana de Menezes, H. M. T. Batista, Luiz Arthur Bevilaqua Bandeira, Antonio Marlos Duarte de Melo, G. Oliveira\",\"doi\":\"10.14295/AIMJ.V2I4.39\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Rett syndrome has yielded many articles over the years since its discovery. This is a production that aims to recover some concepts already brought by other authors, to fix the genetic aspect of the affection, as well as the clinical evolution and associated diseases. Methodology: The screen study is the result of consultations in national and international databases, most notably PubMed and Scielo as a source of academic articles. In the consultations we used the following keywords: Rett Syndrome, Mental Deficit, Multiple Deficit, Epileptic Crisis, and Genetics, we still serve three journals: Genomics & Genetics Weekly, Genetic, Social and General Psychology Monographs and Journal of Medical Genetics of the English equivalent as descriptors: Rett Syndrome, Mental Limitation, General Limitation, Epilepsy and Genetics. In our consultation we found 185 articles and of these, we use 32 to compose our bibliographic reference.  Keywords: Rett syndrome. Mental deficiency. Multiple Deficit. Epileptic\",\"PeriodicalId\":315563,\"journal\":{\"name\":\"Amadeus International Multidisciplinary Journal\",\"volume\":\"98 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-07-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Amadeus International Multidisciplinary Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14295/AIMJ.V2I4.39\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Amadeus International Multidisciplinary Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14295/AIMJ.V2I4.39","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

自从Rett综合征被发现以来,多年来已经发表了许多文章。这是一部旨在恢复其他作者已经提出的一些概念的作品,以确定情感的遗传方面,以及临床演变和相关疾病。方法:筛选研究是在国家和国际数据库中咨询的结果,最著名的是PubMed和Scielo作为学术文章的来源。在咨询中,我们使用以下关键词:Rett综合征,精神缺陷,多重缺陷,癫痫危机和遗传学,我们仍然提供三种期刊:基因组学与遗传学周刊,遗传,社会和普通心理学专著和医学遗传学杂志的英文等效描述:Rett综合征,精神限制,一般限制,癫痫和遗传学。在我们的咨询中,我们找到了185篇文章,我们用其中的32篇来组成我们的参考书目。关键词:Rett综合征;智力缺陷。多个赤字。癫痫
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RELATED ASPECTS OF CLINICAL GENETICS AND RETT SYNDROME EVOLUTION
Rett syndrome has yielded many articles over the years since its discovery. This is a production that aims to recover some concepts already brought by other authors, to fix the genetic aspect of the affection, as well as the clinical evolution and associated diseases. Methodology: The screen study is the result of consultations in national and international databases, most notably PubMed and Scielo as a source of academic articles. In the consultations we used the following keywords: Rett Syndrome, Mental Deficit, Multiple Deficit, Epileptic Crisis, and Genetics, we still serve three journals: Genomics & Genetics Weekly, Genetic, Social and General Psychology Monographs and Journal of Medical Genetics of the English equivalent as descriptors: Rett Syndrome, Mental Limitation, General Limitation, Epilepsy and Genetics. In our consultation we found 185 articles and of these, we use 32 to compose our bibliographic reference.  Keywords: Rett syndrome. Mental deficiency. Multiple Deficit. Epileptic
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信