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11. Screening of congenital hypothyroidism, phenylketonuria, galactosemia, homocystinuria, and maple syrup urine disease in moderate to severe mentally retarded Chinese children. Hsiao KJ, Chen CH, Liu TT, Wu SJ, Plettner C, Clemens P. Taiwan Yi Xue Hui Za Zhi; 1989 Jan; 88(1):18-22. PubMed ID: 2787833 [Abstract] [Full Text] [Related]
12. Inborn errors of metabolism: the need for sugar. Francis DE. J Hum Nutr; 1979 Apr; 33(2):146-54. PubMed ID: 438511 [No Abstract] [Full Text] [Related]
14. [Dietetics in hereditary enzyme deficiencies]. Royer P. Sem Hop; 1970 Feb 26; 46(10):653-9. PubMed ID: 4314674 [No Abstract] [Full Text] [Related]
15. Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study. Humangenetik; 1975 Dec 23; 30(4):273-86. PubMed ID: 1218857 [No Abstract] [Full Text] [Related]
16. Laboratory approaches for inherited neurometabolic diseases. Kolodny EH, Yatziv S. Dev Med Child Neurol; 1985 Apr 23; 27(2):252-7. PubMed ID: 3996782 [No Abstract] [Full Text] [Related]