[Neonatal screening program. Personal experience].
作者信息
Gandolfo Caramello M T, Fogli L, Guala G
出版信息
Minerva Pediatr. 1978 Jun 30;30(12):989-1001.
PMID:672845
Abstract
摘要
相似文献
1
[Neonatal screening program. Personal experience].
Minerva Pediatr. 1978 Jun 30;30(12):989-1001.
2
Phenylketonuria and neonatal hypothyroidism in Spain. Priority of screening for neonatal hypothyroidism.
Eur J Pediatr. 1980 May;133(3):297. doi: 10.1007/BF00496094.
3
[Pilot experiment concerning the concomitant detection of congenital hypothyroidism and phenylketonuria in newborn infants in a high-risk geographical zone. (Results for the year 1979)].[关于在高危地理区域对新生儿先天性甲状腺功能减退症和苯丙酮尿症进行联合检测的试点实验。（1979年的结果）]
Rev Pediatr Obstet Ginecol Pediatr. 1980 Apr-Jun;29(2):131-8.
4
[Mass screening for congenital hypothyroidism in newborn infants in a test area].
Ned Tijdschr Geneeskd. 1980 Feb 23;124(8):260-3.
5
Neonatal hypothyroidism, phenylketonuria and galactosemia screening in metropolitan Shanghai.上海市中心城区新生儿甲状腺功能减退症、苯丙酮尿症和半乳糖血症筛查
Chin Med J (Engl). 1984 Jan;97(1):61-5.
6
[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.
7
State screening for metabolic disorders in newborns.新生儿代谢紊乱的国家筛查。
Am Fam Physician. 1988 Apr;37(4):223-8.
8
[Neonatal screening in hypothyroidism].
Minerva Pediatr. 1979 Apr 15;31(7):497-506.
9
Neonatal screening of phenylketonuria and congenital hypothyroidism in China.中国新生儿苯丙酮尿症和先天性甲状腺功能减退症筛查
Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:17-9.
10
[Neonatal screening for congenital hypothyroidism and phenylketonuria].新生儿先天性甲状腺功能减退症和苯丙酮尿症筛查
Salud Publica Mex. 1994 May-Jun;36(3):249-56.
Zotero 插件