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Journal Abstract Search
255 related items for PubMed ID: 856539
21. [Hereditary amino acid metabolism disorders. Indications for early diagnosis]. Kroll S, Zebisch P, Toussaint W. Fortschr Med; 1972 Apr 13; 90(11):423-8. PubMed ID: 4680607 [No Abstract] [Full Text] [Related]
22. [Early diagnosis of congenital metabolic diseases]. Steuer W. Cah Med; 1971 Oct 15; 12(12):1009-13. PubMed ID: 5130231 [No Abstract] [Full Text] [Related]
26. Perinatal diagnosis of the inborn errors of metabolism. Elsas LJ. J Med Assoc Ga; 1971 Sep 15; 60(9):308-11. PubMed ID: 5093796 [No Abstract] [Full Text] [Related]
27. Diagnostic challenges of aminoacidopathies and organic acidemias in a developing country: a twelve-year experience. Karam PE, Habbal MZ, Mikati MA, Zaatari GE, Cortas NK, Daher RT. Clin Biochem; 2013 Dec 15; 46(18):1787-92. PubMed ID: 23994778 [Abstract] [Full Text] [Related]
30. Newborn screening for hereditary metabolic disorders in Manitoba, 1965-1970. Fox JG, Hall DL, Haworth JC, Maniar A, Sekla L. Can Med Assoc J; 1971 Jun 19; 104(12):1085-8. PubMed ID: 5580751 [Abstract] [Full Text] [Related]
31. [Austrian programm for the early detection of inborn errors of metabolism]. Thalhammer O, Scheibenreiter S, Biedl E. Wien Klin Wochenschr; 1970 Jan 02; 82(1):1-6. PubMed ID: 5513195 [No Abstract] [Full Text] [Related]
36. 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 Jan 02; 12(3):341-8. PubMed ID: 7294941 [Abstract] [Full Text] [Related]