Neonatal screening in Europe; the situation in 2004

Journal of Inherited Metabolic Disease

Volumn 30, Issue 4, 2007, Pages 430-438

  Loeber, J Gerard ^a  

^a NATIONAL INSTITUTE FOR PUBLIC HEALTH AND THE ENVIRONMENT   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTINIDASE DEFICIENCY; CONFERENCE PAPER; CONGENITAL ADRENAL HYPERPLASIA; CONGENITAL HYPOTHYROIDISM; CYSTIC FIBROSIS; EUROPE; GALACTOSEMIA; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEALTH PROGRAM; HUMAN; INBORN ERROR OF METABOLISM; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE DEFICIENCY; NEWBORN; NEWBORN SCREENING; PHENYLKETONURIA; PREVALENCE; SICKLE CELL ANEMIA; TANDEM MASS SPECTROMETRY;

ACYL-COA DEHYDROGENASE; ADRENAL HYPERPLASIA, CONGENITAL; BIOTINIDASE DEFICIENCY; CONGENITAL HYPOTHYROIDISM; CYSTIC FIBROSIS; EUROPE; GALACTOSEMIAS; HUMANS; INFANT, NEWBORN; INSURANCE, HEALTH; NEONATAL SCREENING; PHENYLKETONURIAS;

EID: 34548488231     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-007-0644-5     Document Type: Conference Paper

References (4)

1. Loeber JG, Zabransky S (2004) Newborn screening in Europe: Results of a survey. Proceedings of the Newborn Screening and Genetic Testing Symposium, Atlanta 2004, 205.
2. Mikelsaar RV, Zordania R, Viikmaa M, Kudrjavtseva G (1998) Neonatal screening for congenital hypothyroidism in Estonia. J Med Screen 5: 20-21.
3. Watson MS, Mann MY, Lloyd-Puryear MA, Rinaldo P, Howell RR (American College of Medical Genetics Newborn Screening Expert Group) (2006) Newborn screening: Toward a uniform screening panel and system'Executive summary. Pediatrics 117: S296-S307.
4. Zabransky S (2002) Newborn screening for endocrine and metabolic diseases in Europe 2000. Screening J 2: 1-14.