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objectTitle=Neurology：北京天坛医院神经外科团队新成果——脑动静脉畸形患者De Novo和罕见基因变异的外显子全序列分析, objectType=article, longId=725535, objectId=fb6be2553530, topicUrl=null, isHasObj=0, objectCover=null, objectUrl=/article/show_article.do?id=fb6be2553530, replyNumber=0, likeNumber=99, createdTime=2022-04-28, rootId=0, userName=柳叶一刀, userId=778d36, projectId=1, avatar=, status=1, hasArticle=1, attachment=null, ipAttribution=, moduleDTOList=[ModuleDTO(moduleId=fb6be2553530, moduleTitle=Neurology：北京天坛医院神经外科团队新成果——脑动静脉畸形患者De Novo和罕见基因变异的外显子全序列分析, moduleType=article, hrefUrl=https://www.medsci.cn/article/show_article.do?id=fb6be2553530)], followStatus=false, userIsMember=false, type=1, lengthMark=0)] 梅斯话题小助手

罕见

2020-05-29

syscxl (审核中...)

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#罕见#

儿童神经系统罕见病基因诊断策略的选择与应用

2022-09-16

syscxl (审核中...)

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#罕见#

儿童神经系统罕见病的基因诊断与诊疗方案制定

2022-09-16

syscxl (审核中...)

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#罕见#

罕见病例分享！1例毗邻颗粒链菌引起的法洛四联症患者感染性心内膜炎病例

2022-09-13

syscxl (审核中...)

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2022第十一届中国罕见病高峰论坛在上海隆重举办

2022-09-06

syscxl (审核中...)

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罕见病药物「依库珠单抗」在华收获里程碑进展，为罕见病治疗提供新选择

2022-09-02

syscxl (审核中...)

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#罕见#

罕见病指南的制订：现状、挑战与机遇

2022-08-27

syscxl (审核中...)

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#罕见#

科研愈见未来，2022首届中国罕见病科研及转化医学大会即将在杭州盛大开幕

2022-08-26

syscxl (审核中...)

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#罕见#

罕见病患者信息登记系统（免费）

2022-08-25

syscxl (审核中...)

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威廉姆斯综合征：一种社交达人罕见病

2022-08-17

syscxl (审核中...)

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#罕见#

Dravet综合征：一种可治疗的罕见病

2022-08-17

syscxl (审核中...)

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#罕见#

Nature发布15万人全基因组测序研究成果，揭示多个罕见变异的性状关联

2022-08-10

syscxl (审核中...)

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#罕见#

INC科普·脑瘤连载 | 罕见“虎纹征”小脑发育不良性神经节细胞瘤（Lhermitte-Duclos病）

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syscxl (审核中...)

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关注罕见病：7-7世界卡尔曼氏综合征日

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病例分享| 解开迷雾：一例罕见胃肠道息肉病

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syscxl (审核中...)

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JAMA Cardiol：心肌病和心律失常相关基因罕见变异会增加早发型房颤患者的死亡率

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JAMA Cardiol：与肥厚型心肌病易感性相关的罕见和常见遗传变异

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翻墙骨折不愈发现的一例罕见M3

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罕见病新药7年市场独占权，中华人民共和国药品管理法实施条例（修订草案征求意见稿）发布

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J Hepatol：辉瑞mRNA新冠疫苗可能引发一种罕见的以T细胞为介导的自身免疫性肝炎

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Neurology：北京天坛医院神经外科团队新成果——脑动静脉畸形患者De Novo和罕见基因变异的外显子全序列分析

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