188 related articles for article (PubMed ID: 4427648)
1. Massachusetts Department of Public Health. Cost-benefit analysis of newborn screening for metabolic disorders.
N Engl J Med; 1974 Dec; 291(26):1414-6. PubMed ID: 4427648
[No Abstract] [Full Text] [Related]
2. Newborn screening for metabolic disorders.
Mamunes P
Clin Perinatol; 1976 Mar; 3(1):231-50. PubMed ID: 821691
[No Abstract] [Full Text] [Related]
3. Newborn genetic screening as a concept in health care delivery: a critique.
Lappé M; Roblin RO
Birth Defects Orig Artic Ser; 1974; 10(6):1-23. PubMed ID: 4219872
[No Abstract] [Full Text] [Related]
4. [Screening of newborn infants for inborn errors of metabolism].
Halvorsen S; Skjelkvåle L
Tidsskr Nor Laegeforen; 1970 Jan; 90(2):233-5. PubMed ID: 5430194
[No Abstract] [Full Text] [Related]
5. Editorial: Newborn metabolic screening: past and prospect.
Levy HL
N Engl J Med; 1975 Oct; 293(16):824-5. PubMed ID: 1160974
[No Abstract] [Full Text] [Related]
6. Austria newborn screening programme for inborn errors of metabolism.
Thalhammer O
Acta Univ Carol Med Monogr; 1973; 56():79-82. PubMed ID: 4791784
[No Abstract] [Full Text] [Related]
7. [After PKU and hypothyroidism, what other screening?].
Frézal J; Briard ML; Saudubray JM
J Genet Hum; 1981 Mar; 29(1):47-57. PubMed ID: 7334341
[No Abstract] [Full Text] [Related]
8. Screening for inborn errors of metabolism. Report of a WHO Scientific Group.
World Health Organ Tech Rep Ser; 1968; 401():1-57. PubMed ID: 4973455
[No Abstract] [Full Text] [Related]
9. Massachusetts metabolic disorders screening program. I. Technics and results of urine screening.
Levy HL; Madigan PM; Shih VE
Pediatrics; 1972 Jun; 49(6):825-36. PubMed ID: 5041315
[No Abstract] [Full Text] [Related]
10. [Combined forms of metabolic errors detected in newborn infants].
Tănase-Mogoş I; Ciortoloman H; Grigorescu G; Popescu M; Ankăr V
Physiologie; 1978; 15(4):239-43. PubMed ID: 106407
[No Abstract] [Full Text] [Related]
11. Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria.
Coulombe JT; Shih VE; Levy HL
Pediatrics; 1981 Jan; 67(1):26-31. PubMed ID: 7243433
[TBL] [Abstract][Full Text] [Related]
12. [Early detection of congenital metabolic anomalies].
Thalhammer O
Klin Padiatr; 1973 Mar; 185(2):81-90. PubMed ID: 4576950
[No Abstract] [Full Text] [Related]
13. Diagnosis and treatment: interpreting the positive screening test in the newborn infant.
Scriver CR
Pediatrics; 1967 May; 39(5):764-8. PubMed ID: 6026878
[No Abstract] [Full Text] [Related]
14. [Early diagnosis of congenital disorders].
Méhes K
Orv Hetil; 1978 Jul; 119(30):1819-23. PubMed ID: 353640
[No Abstract] [Full Text] [Related]
15. Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970.
Fox JG; Hall DL; Haworth JC; Maniar A; Sekla L
Can Med Assoc J; 1971 Jun; 104(12):1085-8. PubMed ID: 5580751
[TBL] [Abstract][Full Text] [Related]
16. Urinary screening tests in the infant and young child.
Bradley GM
Hum Pathol; 1971 Jun; 2(2):309-20. PubMed ID: 4256386
[No Abstract] [Full Text] [Related]
17. A biochemical perspective on the use of tandem mass spectrometry for newborn screening and clinical testing.
Chace DH; Kalas TA
Clin Biochem; 2005 Apr; 38(4):296-309. PubMed ID: 15766731
[TBL] [Abstract][Full Text] [Related]
18. Diagnosis and treatment of metabolic errors.
Can Med Assoc J; 1971 Jun; 104(12):1064-5. PubMed ID: 5580749
[No Abstract] [Full Text] [Related]
19. Neonatal screening for biochemical disorders.
Holton JB
Br J Hosp Med; 1988 Apr; 39(4):317-9, 322-4. PubMed ID: 3164641
[TBL] [Abstract][Full Text] [Related]
20. [Changes to be expected in the field of pediatric practice by extensive distribution of mass screening].
Domokos B
Orv Hetil; 1976 Sep; 117(37):2227-30. PubMed ID: 967428
[No Abstract] [Full Text] [Related]
[Next] [New Search]
