Neonatal screening for congenital hypothyroidism in Europe. Report of the Newborn Committee of the European Thyroid Association.

Suppr

超能文献

作者信息

Delange F

出版信息

Acta Endocrinol Suppl (Copenh). 1979;223:3-29.

PMID:285560

Abstract

摘要

相似文献

Neonatal screening for congenital hypothyroidism in Europe. Report of the Newborn Committee of the European Thyroid Association.

Acta Endocrinol Suppl (Copenh). 1979;223:3-29.

Problems in screening for congenital hypothyroidism using thyroxine assays from small dried blood discs.

J Nucl Med. 1981 Sep;22(9):818-23.

Recommendations for screening programs for congenital hypothyroidism: Newborn Committee of the American Thyroid Association.先天性甲状腺功能减退症筛查项目建议：美国甲状腺协会新生儿委员会

Can Med Assoc J. 1977 Mar 19;116(6):631-2.

Screening for congenital hypothyroidism using an insolubilized radio immunoassay technique.

J Indiana State Med Assoc. 1978 Jul;71(7):689-91.

Screening for congenital hypothyroidism: a three year experience.

N Z Med J. 1984 Mar 28;97(752):175-7.

[Mass screening for congenital hypothyroidism in newborn infants in a test area].

Ned Tijdschr Geneeskd. 1980 Feb 23;124(8):260-3.

[Congenital hypothyroidism: metabolic aspects and neonatal screening].[先天性甲状腺功能减退症：代谢方面与新生儿筛查]

Ann Ist Super Sanita. 1979;15(2):325-46.

[Neonatal detection of hypothyroidism in the South-Pyrenean region. Results of 14,000 determinations of T4 in blood eluates collected on blotting-paper].

Arch Fr Pediatr. 1978 Jun-Jul;35(6):589-94.

[Neonatal detection of congenital hypothyroidism by TSH determination in dried blood stain. 2 years of experience].

Nouv Presse Med. 1979 Mar 10;8(11):868.

Adaptation of TSH filter paper method for regionalized screening for congenital hypothyroidism.

J Lab Clin Med. 1977 Jul;90(1):11-7.

引用本文的文献

Segregation of S292F TPO gene mutation in three large Tunisian families with thyroid dyshormonogenesis: evidence of a founder effect.S292F甲状腺过氧化物酶（TPO）基因突变在三个突尼斯甲状腺激素合成障碍大家族中的分离：奠基者效应的证据

Eur J Pediatr. 2015 Nov;174(11):1491-501. doi: 10.1007/s00431-015-2550-4. Epub 2015 May 13.

Need for neonatal screening program in India: A national priority.印度新生儿筛查项目的必要性：一项国家优先事项。

Indian J Endocrinol Metab. 2015 Mar-Apr;19(2):204-20. doi: 10.4103/2230-8210.149315.

Prevalence of c.2268dup and detection of two novel alterations, c.670_672del and c.1186C>T, in the TPO gene in a cohort of Malaysian-Chinese with thyroid dyshormonogenesis.在一个马来西亚华裔甲状腺激素生成障碍的队列中，检测到 TPO 基因中的 c.2268dup 及两个新的突变 c.670_672del 和 c.1186C>T。

BMJ Open. 2015 Jan 5;5(1):e006121. doi: 10.1136/bmjopen-2014-006121.

A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter.马来西亚先天性甲状腺功能减退伴多结节性甲状腺肿姐妹中甲状腺过氧化物酶基因的新型纯合 c.1502T>G (p.Val501Gly) 突变。

Int J Endocrinol. 2013;2013:987186. doi: 10.1155/2013/987186. Epub 2013 Apr 29.

Contribution of genetic factors to neonatal transient hypothyroidism.遗传因素对新生儿暂时性甲状腺功能减退症的影响。

Arch Dis Child Fetal Neonatal Ed. 2005 Jan;90(1):F69-72. doi: 10.1136/adc.2003.039065.

Screening for congenital hypothyroidism.先天性甲状腺功能减退症的筛查。

Arch Dis Child. 1980 Dec;55(12):913-4. doi: 10.1136/adc.55.12.913.

Screening for congenital hypothyroidism in Northern Ireland.

Ir J Med Sci. 1982 Sep;151(9):267-71. doi: 10.1007/BF02940198.

Congenital hypothyroidism.

Indian J Pediatr. 1982 Jul-Aug;49(399):621-8. doi: 10.1007/BF02834570.

Quantitative 123I-iodide scintigraphy and radiation dosimetry in infants with congenital hypothyroidism.先天性甲状腺功能减退症婴儿的定量123I-碘闪烁扫描及辐射剂量测定

Eur J Nucl Med. 1985;11(4):132-5. doi: 10.1007/BF00265047.

Cytogenetic analysis in congenital hypothyroidism.先天性甲状腺功能减退症的细胞遗传学分析。

J Endocrinol Invest. 1990 Jul-Aug;13(7):605-7. doi: 10.1007/BF03348640.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验