• 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

Two distinct syndromic children with T-acute lymphoblastic leukemia: Noonan syndrome and Sotos syndrome.

作者信息

Kaya Zühre, Keser Elifsu, Atalay Ece, Kayhan Gülsüm, Karamercan Sırma, Topuz Büşra, Kirkiz Serap, Koçak Ülker

机构信息

Department of Pediatric Hematology, Gazi University School of Medicine, Ankara, Turkey.

Department of Pediatric Hematology, Gazi University School of Medicine, Ankara, Turkey.

出版信息

Leuk Res. 2022 Dec;123:106981. doi: 10.1016/j.leukres.2022.106981. Epub 2022 Oct 22.

DOI:10.1016/j.leukres.2022.106981
PMID:36356491
Abstract
摘要

相似文献

1
Two distinct syndromic children with T-acute lymphoblastic leukemia: Noonan syndrome and Sotos syndrome.两名患有T细胞急性淋巴细胞白血病的不同综合征患儿:努南综合征和索托斯综合征。
Leuk Res. 2022 Dec;123:106981. doi: 10.1016/j.leukres.2022.106981. Epub 2022 Oct 22.
2
Neurofibromatosis-Noonan syndrome and acute lymphoblastic leukemia: a report of two cases.神经纤维瘤病-努南综合征与急性淋巴细胞白血病:两例报告
J Pediatr Hematol Oncol. 1999 Mar-Apr;21(2):158-60. doi: 10.1097/00043426-199903000-00014.
3
Acute lymphoblastic leukemia in the context of RASopathies.RAS病相关的急性淋巴细胞白血病
Eur J Med Genet. 2016 Mar;59(3):173-8. doi: 10.1016/j.ejmg.2016.01.003. Epub 2016 Feb 5.
4
Acute lymphoblastic leukemia developing in a patient with Noonan syndrome harboring a PTPN11 germline mutation.一名患有努南综合征且携带PTPN11种系突变的患者发生急性淋巴细胞白血病。
J Pediatr Hematol Oncol. 2014 Mar;36(2):e136-9. doi: 10.1097/MPH.0000000000000002.
5
Acute lymphoblastic leukemia in Noonan syndrome: report of two cases.努南综合征合并急性淋巴细胞白血病:两例报告
Med Pediatr Oncol. 1993;21(6):454-5. doi: 10.1002/mpo.2950210613.
6
Mutations in RIT1 cause Noonan syndrome with possible juvenile myelomonocytic leukemia but are not involved in acute lymphoblastic leukemia.RIT1基因的突变会导致伴有幼年型粒单核细胞白血病可能性的努南综合征,但不参与急性淋巴细胞白血病的发生。
Eur J Hum Genet. 2016 Aug;24(8):1124-31. doi: 10.1038/ejhg.2015.273. Epub 2016 Jan 13.
7
[Noonan syndrome associated with acute lymphoblastic leukosis].[与急性淋巴细胞白血病相关的努南综合征]
An Esp Pediatr. 1982 Jul;17(1):78-80.
8
Occurrence of acute lymphoblastic leukemia and juvenile myelomonocytic leukemia in a patient with Noonan syndrome carrying the germline PTPN11 mutation p.E139D.患者携带 PTPN11 基因突变 p.E139D,患有努南综合征,同时发生急性淋巴细胞白血病和幼年型粒单核细胞白血病。
Am J Med Genet A. 2012 Mar;158A(3):652-8. doi: 10.1002/ajmg.a.34439. Epub 2012 Feb 7.
9
Neurofibromatosis with fully expressed Noonan syndrome.伴有完全表现型努南综合征的神经纤维瘤病。
Am J Med Genet. 1988 Apr;29(4):937-41. doi: 10.1002/ajmg.1320290426.
10
Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.一名努南综合征患者的急性淋巴细胞白血病原始细胞中,由于获得性单亲二体导致种系PTPN11突变的克隆性复制。
Leukemia. 2007 Jun;21(6):1303-5. doi: 10.1038/sj.leu.2404651. Epub 2007 Mar 15.

引用本文的文献

1
Transient Myeloproliferative Disorder (TMD), Acute Lymphoblastic Leukemia (ALL), and Juvenile Myelomonocytic Leukemia (JMML) in a Child with Noonan Syndrome: Sequential Occurrence, Single Center Experience, and Review of the Literature.儿童神经纤维瘤病相关先天性中胚层肾瘤:附 1 例报告并文献复习
Genes (Basel). 2024 Sep 10;15(9):1191. doi: 10.3390/genes15091191.
2
Beyond the known phenotype of sotos syndrome: a 31-individuals cohort study.超越索托斯综合征的已知表型:一项31例个体的队列研究。
Front Pediatr. 2023 Jun 13;11:1184529. doi: 10.3389/fped.2023.1184529. eCollection 2023.