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22. Inherited metabolic disorders: from the newborn to the mother and beyond. Levy HL Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():119-20. PubMed ID: 11400747 [No Abstract] [Full Text] [Related]
23. 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]
28. [Screening for congenital metabolic disorders. Indication and results]. Bickel H Monatsschr Kinderheilkd; 1983 Jun; 131(6):323-7. PubMed ID: 6888386 [No Abstract] [Full Text] [Related]
29. 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]
30. [Detection of metabolic diseases]. Adriaenssens K; Van Sande M Acta Neurol Psychiatr Belg; 1968 Oct; 68(10):719-28. PubMed ID: 4976725 [No Abstract] [Full Text] [Related]
36. Nutrition in the management of inborn errors of metabolism. Dashman T; Sansaricq C Clin Lab Med; 1993 Jun; 13(2):407-32. PubMed ID: 8319427 [TBL] [Abstract][Full Text] [Related]
37. Diagnosis and treatment of metabolic errors. Can Med Assoc J; 1971 Jun; 104(12):1064-5. PubMed ID: 5580749 [No Abstract] [Full Text] [Related]
38. [Metabolic disorders and functional disorders of the brain]. Kakimoto Y Shinkei Kenkyu No Shimpo; 1966 Oct; 10(3):480-3. PubMed ID: 6009298 [No Abstract] [Full Text] [Related]
39. [Enzyme activity and the character of metabolic changes in brain tissue in children with phenylketonuria and histidinemia]. Barasnĕv J Cesk Pediatr; 1980; 35(2):49-52. PubMed ID: 7371094 [No Abstract] [Full Text] [Related]
40. [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] [Previous] [Next] [New Search]