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9. The critically ill child: acute metabolic disease in infancy and early childhood. O'Brien D; Goodman SI Pediatrics; 1970 Oct; 46(4):620-6. PubMed ID: 5503697 [No Abstract] [Full Text] [Related]
10. Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease. Vaca G; Hernández A; Ibarra B; Velázquez A; Olivares N; Sanchez-Corona J; Medina C; Cantú JM Arch Invest Med (Mex); 1981; 12(3):341-8. PubMed ID: 7294941 [TBL] [Abstract][Full Text] [Related]
11. [Metabolic disorders, their early diagnosis and therapy in newborn infants]. Tabolin VA Vestn Akad Med Nauk SSSR; 1973; 28(6):76-86. PubMed ID: 4729650 [No Abstract] [Full Text] [Related]
12. [Suspected clinical diagnosis of genetic metabolic disorders in prevention and daily practice]. Grosser V; Knapp A Z Arztl Fortbild (Jena); 1973 Dec; 67(24):1233-8. PubMed ID: 4791811 [No Abstract] [Full Text] [Related]
13. Dyskinesia and dystonia in neurometabolic disorders. Hagberg B; Kyllerman M; Steen G Neuropadiatrie; 1979 Nov; 10(4):305-20. PubMed ID: 583441 [No Abstract] [Full Text] [Related]
14. [Mass screening of genetic metabolic abnormalities with special reference to amino acid metabolism disorders, using chemical methods]. Lubs H; Knapp A Z Arztl Fortbild (Jena); 1970 May; 64(10):516-9. PubMed ID: 5520559 [No Abstract] [Full Text] [Related]
15. [Biochemical diagnosis and therapy of molecular diseases]. Perlès R Ann Pharm Fr; 1974 Feb; 32(2):155-70. PubMed ID: 4433116 [No Abstract] [Full Text] [Related]
16. [Studies of inborn errors of amino acid metabolism and urinary excretion of -phenylethylamine, using screening methods]. Berio A Minerva Pediatr; 1972 Jun; 24(32):937-41. PubMed ID: 5050421 [No Abstract] [Full Text] [Related]
17. 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]