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3. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism]. Charpentier C; Lemonnier A Ann Biol Clin (Paris); 1969; 27(5):297-323. PubMed ID: 4897889 [No Abstract] [Full Text] [Related]
4. [Aminoacid metabolism disorders in infancy with special reference to phenylketonuria. II. Aminoacid metabolism and general physiopathology of aminoacidopathies]. Segni G Minerva Nipiol; 1970; 20(4):83-110. PubMed ID: 4396023 [No Abstract] [Full Text] [Related]
5. Recent advances in the early detection and treatment of inborn errors with brain damage. Bickel H Neuropadiatrie; 1969; 1(1):1-11. PubMed ID: 4942066 [No Abstract] [Full Text] [Related]
6. The assessment of serum amino acids. Swallow WH; Carrell RW N Z Med J; 1970 Feb; 71(453):85-8. PubMed ID: 5267129 [No Abstract] [Full Text] [Related]
7. Rapid screening methods for the detection of inherited and acquired aminoacidopathies. Saifer A Adv Clin Chem; 1971; 14():145-218. PubMed ID: 4109903 [No Abstract] [Full Text] [Related]
8. Neonatal screening for inborn errors of amino acid metabolism. Levy HL Clin Endocrinol Metab; 1974 Mar; 3(1):153-66. PubMed ID: 4609646 [No Abstract] [Full Text] [Related]
9. Screening for hyperaminoacidemias in newborns by thin-layer chromatography on DEAE-cellulose. Vercaemst R; Blaton V; Lievens-Taveirne J; Peeters H Acta Paediatr Belg; 1973; 27(5):334-47. PubMed ID: 4779694 [No Abstract] [Full Text] [Related]
10. Ion-exchange thin-layer chromatographic screening test for phenylketonuria and other aminoacidaemias. Kovács J Acta Paediatr Acad Sci Hung; 1973; 14(3):165-9. PubMed ID: 4785695 [No Abstract] [Full Text] [Related]
11. [The inborn errors of metabolism of amino acids]. Tomaszewski L Postepy Biochem; 1973; 19(1):91-122. PubMed ID: 4697972 [No Abstract] [Full Text] [Related]
12. American Academy of Pediatrics. Committee on Nutrition: special diets for infants with inborn errors of amino acid metabolism. Pediatrics; 1976 May; 57(5):783-92. PubMed ID: 940719 [TBL] [Abstract][Full Text] [Related]