Lessons from the past - Looking for the future. Newborn screening

Pediatric Annals

Volumn 32, Issue 8, 2003, Pages 505-508

  Levy, Harvey L ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE;

ALPHA 1 ANTITRYPSIN DEFICIENCY; COMBINED IMMUNODEFICIENCY; DIET RESTRICTION; FRAGILE X SYNDROME; HEMOCHROMATOSIS; HISTIDINEMIA; HUMAN; HYPOTHYROIDISM; INCIDENCE; INSULIN DEPENDENT DIABETES MELLITUS; LYMPHATIC LEUKEMIA; MENTAL DEFICIENCY; NEWBORN SCREENING; PHENYLKETONURIA; REVIEW;

EID: 0041528191     PISSN: 00904481     EISSN: None     Source Type: Journal    
DOI: 10.3928/0090-4481-20030801-07     Document Type: Review

References (26)

1. Guthrie R. The origin of newborn screening. Screening. 1992;1:5-15.
2. Bickel H, Gerrard J, Hickmans E. Influence of phenylalanine intake on phenylketonuria. Lancet. 1953;ii:812-813.
3. Horner F, Streamer CW. Phenylketonuria treated from earliest infancy. AJDC. 1959;97:345-347.
4. Armstrong M, Low NL, Bosma JF. Studies on phenylketonuria, IX. Further observations on the effect of phenylalanine-restricted diet on patients with phenylketonuria. Amer J Clin Nutr. 1957;5:543-554.
5. MacCready R. Phenylketonuria screening program. N Engl J Med. 1963;269:52.
6. Andrews L. State Laws and Regulations Governing Newborn Screening. Chicago: American Bar Association; 1985.
7. Kennedy JL Jr., Wertelecki W, Gates L, Sperry BP, Cass VM. The early treatment of phenylketonuria. AJDC. 1967;113:16-21.
8. Guthrie R. Screening for "inborn errors of metabolism" in the new born infant - a multiple test program. Birth Def Orig Art Ser. 1968;4:92-96.
9. Dussault JH, Coulombe P, Laberge C, et al. Preliminary report on a mass screening program for neonatal hypothyroidism. J Pediatr. 1975;86:670-674.
10. Delange F. Neonatal screening for congenital hypothyroidism: results and perspectives. Horm Res. 1997;48:51-61.
11. Simons WF, Fuggle PW, Grant DB, Smith I. Intellectual development at 10 years in early treated congenital hypothyroidism. Arch Dis Child. 1994;71:232-234.
12. Garrick MD, Dembure P, Guthrie R. Sickle-cell anemia and other hemglobinopathies. Procedures and strategy for screening employing spots of blood on filter paper as specimens. N Engl J Med. 1973;288:1265-1268.
13. Pang S, Hotchkiss J, Drash AL, et al. Microfilter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay: its application for rapid screening for congenital adrenal hyperplasia. J Clin Endocrinol 1977;45:1003-1008.
14. Heard GS, Secor McVoy JR, Wolf B. A screening method for biotinidase deficiency in newborns. Clin Chem. 1984;30:125-127.
15. Guerina NG, Hsu HW, Meissner HC, et al. Neonatal serologic screening and early treatment for congenital Toxoplasma gondii infection. The New England Regional Toxoplasma Working Group. New Engl J Med. 1994;330:1858-1863.
16. Levy HL. Newborn screening by tandem mass spectrometry: a new era. Clin Chem. 1998;44:2401-2402.
17. Wood JC, Magera MJ, Rinaldo P, Seashore MR, Strauss AW, Friedman A. Diagnosis of very long chain acyl-dehydrogenase deficiency from an infant's newborn screening card. Pediatrics. 2001;108:E19.
18. McCabe LL, McCabe ER. Newborn screening as a model for population screening. Mol Genet Metab. 2002;75:299-307.
19. Ross L. Minimizing risks: The ethics of predictive diabetes mellitus screening research in newborns. Arch Pediatr Adolesc Med. 2003;157:89-95.
20. Workshop to Develop Newborn Screening Technology for SCID. National Institutes of Health. July 25-26, 2002.
21. Merryweather-Clarke AT, Simonsen H, Shearman JD, Pointon JJ, Norgaard-Pedersen B, Robson KJ. A retrospective anonymous pilot study in screening newborns for HFE mutations in Scandinavian populations. Hum Mutat. 1999;13:154-159.
22. Gale KB, Ford AM, Repp R, et al. Backtracking leukemia to birth: identification of clonotypic gene fusion sequences in neonatal blood spots. Proc Natl Acad Sci USA. 1997;94:13950-13954.
23. Levy HL, Shih VE, Madigan PM. Routine newborn screening for hisfidinemia. Clinical and biochemical results. N Engl J Med. 1974;291:1214-1219.
24. McNeil TF, Thelin T, Aspegren-Jansson E, Sveger T. Identifying children at high somatic risk: possible effects on the parents' views of the child's health and parents' relationship to the pediatric health services. Acta Psychiatr Scand. 1985;72:491-497.
25. Vohr BR, Carty LM, Moore PE, Letourneau K. The Rhode Island Hearing Assessment Program: experience with statewide hearing screening (1993-1996). J Pediatr 1998;133:353-357.
26. Newborn screening: A blueprint for the future executive summary: newborn screening task force report. Pediatrics. 2000;106:386-388.