• 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

Subtle anomalies of the septum pellucidum and neurodevelopmental deficits.

作者信息

Schaefer G B, Bodensteiner J B, Thompson J N

机构信息

Meyer Rehabilitation Institute, University of Nebraska Medical Center, Omaha 68198-5430.

出版信息

Dev Med Child Neurol. 1994 Jun;36(6):554-9. doi: 10.1111/j.1469-8749.1994.tb11888.x.

DOI:10.1111/j.1469-8749.1994.tb11888.x
PMID:7516298
Abstract
摘要

相似文献

1
Subtle anomalies of the septum pellucidum and neurodevelopmental deficits.透明隔的细微异常与神经发育缺陷。
Dev Med Child Neurol. 1994 Jun;36(6):554-9. doi: 10.1111/j.1469-8749.1994.tb11888.x.
2
Wide cavum septum pellucidum: a marker of disturbed brain development.透明隔腔增宽：脑发育异常的一个标志。
Pediatr Neurol. 1990 Nov-Dec;6(6):391-4. doi: 10.1016/0887-8994(90)90007-n.
3
[Agenesis septum pellucidum in a schizophrenic patient].[一名精神分裂症患者的透明隔缺如]
Nervenarzt. 1999 Mar;70(3):269-75. doi: 10.1007/s001150050433.
4
Radiological studies in rare but typical cerebral malformations; encephalographic findings in cerebral hemiagenesis, absence of corpus callosum and absence of septum pellucidum.
Stanford Med Bull. 1948 Aug;6(3):395-406.
5
Ultrasound evaluation of septo-optic dysplasia in the new born. Report of a case.
Neuroradiology. 1986;28(5-6):491-2. doi: 10.1007/BF00344102.
6
Imaging the corpus callosum, septum pellucidum and fornix in children: normal anatomy and variations of normality.儿童胼胝体、透明隔和穹窿的影像学表现：正常解剖结构及正常变异
Neuroradiology. 2009 May;51(5):337-45. doi: 10.1007/s00234-009-0506-y. Epub 2009 Mar 7.
7
Diabetes insipidus with impaired osmotic regulation in septo-optic dysplasia and agenesis of the corpus callosum.伴有渗透压调节受损的尿崩症见于视隔发育不良和胼胝体发育不全。
Arch Dis Child. 1994 Jan;70(1):51-3. doi: 10.1136/adc.70.1.51.
8
The identification of agenesis of the septum pellucidum by ventriculography in eleven infants.通过脑室造影术对11例婴儿透明隔缺如的鉴定。
Acta Univ Carol Med Monogr. 1976(75):157-9.
9
[MR in the evaluation of schizencephaly].[磁共振成像在无脑回畸形评估中的应用]
Radiol Med. 1989 Oct;78(4):311-3.
10
Absent cavum with intact septum pellucidum and corpus callosum may indicate midline brain abnormalities.透明隔腔缺如但透明隔和胼胝体完整可能提示中线脑异常。
Ultrasound Obstet Gynecol. 2013 Mar;41(3):343-4. doi: 10.1002/uog.12402.

引用本文的文献

1
Major brain malformations: corpus callosum dysgenesis, agenesis of septum pellucidum and polymicrogyria in patients with BCORL1-related disorders.主要脑部畸形：脑-胼胝体发育不良、透明隔发育不全和多小脑回畸形，见于 BCORL1 相关疾病患者。
J Hum Genet. 2022 Feb;67(2):95-101. doi: 10.1038/s10038-021-00971-5. Epub 2021 Aug 16.
2
Antenatal diagnosis of absence of septum pellucidum.透明隔缺如的产前诊断。
Clin Case Rep. 2020 Feb 5;8(3):498-503. doi: 10.1002/ccr3.2666. eCollection 2020 Mar.
3
Brain Malformations Do Not Predict Hypopituitarism in Young Children with Optic Nerve Hypoplasia.
脑畸形不会预测伴有视神经发育不良的幼儿的垂体功能减退症。
Horm Res Paediatr. 2017;88(3-4):251-257. doi: 10.1159/000479029. Epub 2017 Aug 22.
4
Dissociated repetition deficits in aphasia can reflect flexible interactions between left dorsal and ventral streams and gender-dimorphic architecture of the right dorsal stream.失语症中的分离重复缺陷可以反映左背侧和腹侧流之间的灵活相互作用以及右背侧流的性别二态结构。
Front Hum Neurosci. 2013 Dec 19;7:873. doi: 10.3389/fnhum.2013.00873. eCollection 2013.
5
Prenatal infection and cavum septum pellucidum in adult schizophrenia.成人精神分裂症中的产前感染与透明隔腔
Schizophr Res. 2009 Mar;108(1-3):285-7. doi: 10.1016/j.schres.2008.11.018. Epub 2009 Jan 8.
6
Cavum septum pellucidum in schizophrenia: clinical and neuropsychological correlates.精神分裂症中的透明隔腔：临床与神经心理学关联
Psychiatry Res. 2007 Feb 28;154(2):147-55. doi: 10.1016/j.pscychresns.2006.09.001. Epub 2007 Feb 7.
7
The septum pellucidum and its variants. An MRI study.透明隔及其变异：一项MRI研究
Eur Arch Psychiatry Clin Neurosci. 2004 Oct;254(5):295-302. doi: 10.1007/s00406-004-0496-z.
8
Qualitative MRI findings in adults with 22q11 deletion syndrome and schizophrenia.22q11缺失综合征合并精神分裂症成人患者的MRI定性研究结果
Biol Psychiatry. 1999 Nov 15;46(10):1436-42. doi: 10.1016/s0006-3223(99)00150-x.
9
Dominantly inherited cerebral dysplasia: arachnoid cyst associated with mild mental handicap in a mother and her son.显性遗传性脑发育异常：一位母亲及其儿子患有蛛网膜囊肿并伴有轻度智力障碍
J Med Genet. 1997 Dec;34(12):1018-20. doi: 10.1136/jmg.34.12.1018.