A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER

M L EFRON et al. N Engl J Med. 1964.

. 1964 Jun 25:270:1378-83.

doi: 10.1056/NEJM196406252702602.

No abstract available

Cited by

Phenylketonuria in Kuwait and Arab countries.
Teebi AS, Al-Awadi SA, Farag TI, Naguib KK, el-Khalifa MY. Teebi AS, et al. Eur J Pediatr. 1987 Jan;146(1):59-60. doi: 10.1007/BF00647286. Eur J Pediatr. 1987. PMID: 3582406
Routine neonatal screening for phenylketonuria in the United Kingdom 1964-78. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register.
[No authors listed] [No authors listed] Br Med J (Clin Res Ed). 1981 May 23;282(6277):1680-4. doi: 10.1136/bmj.282.6277.1680. Br Med J (Clin Res Ed). 1981. PMID: 6786433 Free PMC article.
Newborn screening in North America.
Therrell BL, Adams J. Therrell BL, et al. J Inherit Metab Dis. 2007 Aug;30(4):447-65. doi: 10.1007/s10545-007-0690-z. Epub 2007 Jul 23. J Inherit Metab Dis. 2007. PMID: 17643194
A Commentary on Multiple Screening for Aminoacidopathies in the Newborn Infant.
Scriver CR, Clow C, Davies E, Ramos A, Stern L. Scriver CR, et al. Can Med Assoc J. 1965 Jun 26;92(26):1331-3. Can Med Assoc J. 1965. PMID: 20328261 Free PMC article.
Aminoacidopathies in Andhra Pradesh; report of a screening programme.
Uma SM, Jyothy A, Reddy PP, Reddi OS. Uma SM, et al. J Inherit Metab Dis. 1982;5(4):211-4. doi: 10.1007/BF02179143. J Inherit Metab Dis. 1982. PMID: 6820443