儿童甲状腺疾病临床病例研讨会。

Endocrine development Pub Date : 2014-01-01 Epub Date: 2014-08-29 DOI:10.1159/000363166
G Szinnai, J Léger, A J Bauer, E N Pearce, H E Ramos, M H Canalli, K Onigata, R Elisei, G Radetti, M Polak, G Van Vliet, J Deladoëy
{"title":"儿童甲状腺疾病临床病例研讨会。","authors":"G Szinnai,&nbsp;J Léger,&nbsp;A J Bauer,&nbsp;E N Pearce,&nbsp;H E Ramos,&nbsp;M H Canalli,&nbsp;K Onigata,&nbsp;R Elisei,&nbsp;G Radetti,&nbsp;M Polak,&nbsp;G Van Vliet,&nbsp;J Deladoëy","doi":"10.1159/000363166","DOIUrl":null,"url":null,"abstract":"<p><p>Pediatric thyroid diseases cover a large spectrum of congenital and acquired forms, ranging from congenital primary or central hypothyroidism, autoimmune thyroid disease, iodine deficiency, rare genetic defects of thyroid hormone action, metabolism and cell membrane transport to benign nodules and malignant tumors. The previous 15 papers of the textbook Paediatric Thyroidology gave a systematic overview of the current knowledge and guidelines on all these diseases. In this final paper, the authors collected a series of patient histories from their clinics illustrating frequently encountered clinical problems and providing key learning points and references to each case. Although not fully comprehensive, it aims at providing relevant clinical knowledge on thyroid diseases of the neonate, the child, and the adolescent.</p>","PeriodicalId":72906,"journal":{"name":"Endocrine development","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2014-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1159/000363166","citationCount":"4","resultStr":"{\"title\":\"Clinical case seminar in pediatric thyroid disease.\",\"authors\":\"G Szinnai,&nbsp;J Léger,&nbsp;A J Bauer,&nbsp;E N Pearce,&nbsp;H E Ramos,&nbsp;M H Canalli,&nbsp;K Onigata,&nbsp;R Elisei,&nbsp;G Radetti,&nbsp;M Polak,&nbsp;G Van Vliet,&nbsp;J Deladoëy\",\"doi\":\"10.1159/000363166\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Pediatric thyroid diseases cover a large spectrum of congenital and acquired forms, ranging from congenital primary or central hypothyroidism, autoimmune thyroid disease, iodine deficiency, rare genetic defects of thyroid hormone action, metabolism and cell membrane transport to benign nodules and malignant tumors. The previous 15 papers of the textbook Paediatric Thyroidology gave a systematic overview of the current knowledge and guidelines on all these diseases. In this final paper, the authors collected a series of patient histories from their clinics illustrating frequently encountered clinical problems and providing key learning points and references to each case. Although not fully comprehensive, it aims at providing relevant clinical knowledge on thyroid diseases of the neonate, the child, and the adolescent.</p>\",\"PeriodicalId\":72906,\"journal\":{\"name\":\"Endocrine development\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2014-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1159/000363166\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Endocrine development\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1159/000363166\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2014/8/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine development","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1159/000363166","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2014/8/29 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 4

摘要

儿童甲状腺疾病包括先天性和后天的多种形式,从先天性原发性或中枢性甲状腺功能减退、自身免疫性甲状腺疾病、碘缺乏、甲状腺激素作用、代谢和细胞膜运输的罕见遗传缺陷到良性结节和恶性肿瘤。教科书《儿科甲状腺学》的前15篇论文对所有这些疾病的当前知识和指南进行了系统的概述。在最后一篇论文中,作者从他们的诊所收集了一系列患者的病史,说明了经常遇到的临床问题,并提供了每个病例的关键学习点和参考。虽然不完全全面,但它旨在提供有关新生儿、儿童和青少年甲状腺疾病的临床知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Clinical case seminar in pediatric thyroid disease.

Pediatric thyroid diseases cover a large spectrum of congenital and acquired forms, ranging from congenital primary or central hypothyroidism, autoimmune thyroid disease, iodine deficiency, rare genetic defects of thyroid hormone action, metabolism and cell membrane transport to benign nodules and malignant tumors. The previous 15 papers of the textbook Paediatric Thyroidology gave a systematic overview of the current knowledge and guidelines on all these diseases. In this final paper, the authors collected a series of patient histories from their clinics illustrating frequently encountered clinical problems and providing key learning points and references to each case. Although not fully comprehensive, it aims at providing relevant clinical knowledge on thyroid diseases of the neonate, the child, and the adolescent.

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
期刊最新文献
Transition of Care from Childhood to Adulthood: Turner Syndrome. Fertility Preservation in Endocrine Disorders during Transition for Girls. Management of Hypothalamic Obesity during Transition from Childhood to Adulthood. Transition of Care from Childhood to Adulthood: Congenital Hypogonadotropic Hypogonadism. Challenges of the Transition from Pediatric Care to Care of Adults: "Say Goodbye, Say Hello".
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1