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2. Review of current practices in management of inherited disorders of amino acid metabolism in Western Europe. Wachtel U Hum Nutr Appl Nutr; 1986; 40 Suppl 1():61-9. PubMed ID: 3528074 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. Screening for inborn errors of amino acid metabolism. Wu JT Ann Clin Lab Sci; 1991; 21(2):123-42. PubMed ID: 2029175 [TBL] [Abstract][Full Text] [Related]
5. [Brain function in inborn error of amino acid metabolism]. Takada G Tanpakushitsu Kakusan Koso; 1984 Dec; 29(14):1783-93. PubMed ID: 6398464 [No Abstract] [Full Text] [Related]
6. [Pre- and postnatal diagnosis of organoacidopathies]. Hoffmann GF; Jakobs C; Rating D; Sweetman L; Trefz FK Monatsschr Kinderheilkd; 1990 Jul; 138(7):381-8. PubMed ID: 2204822 [TBL] [Abstract][Full Text] [Related]
7. [Screening of newborns for inborn errors of metabolism by tandem mass spectrometry]. Simonsen H Ugeskr Laeger; 2002 Nov; 164(48):5607-12. PubMed ID: 12523003 [TBL] [Abstract][Full Text] [Related]
8. Screening of amino acid enzymopathies in pregnancy and possibilities of their prenatal diagnosis. Hyánek J; Trnka V; Homolka J; Seemanová E; Macek M; Dolezal A; Wünschová N; Hoza J; Kapras J; Kunová V; Tauchmanová H Acta Univ Carol Med Monogr; 1977; (79 Pt 3):15-21. PubMed ID: 615475 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. [Biochemical studies on inherited disorders of amino acid metabolism in pediatrics]. Antener I Z Klin Chem Klin Biochem; 1970 Sep; 7(5):427-39. PubMed ID: 5505952 [No Abstract] [Full Text] [Related]
11. The dietary management of inborn errors of metabolism. Collins JE; Leonard JV Hum Nutr Appl Nutr; 1985 Aug; 39(4):255-72. PubMed ID: 3900002 [TBL] [Abstract][Full Text] [Related]
12. Brain amino acid reductions in one family with chromosome 6p-linked dominantly inherited olivopontocerebellar atrophy. Kish SJ; Robitaille Y; el-Awar M; Gilbert J; Deck J; Chang LJ; Schut L Ann Neurol; 1991 Dec; 30(6):780-4. PubMed ID: 1686387 [TBL] [Abstract][Full Text] [Related]
13. Hyperphenylalaninemia due to inherited deficiencies of tetrahydrobiopterin. Matalon R; Michals K; Blau N; Rouse B Adv Pediatr; 1989; 36():67-89. PubMed ID: 2675577 [No Abstract] [Full Text] [Related]
14. Free amino acid pattern in the liver from the patients with amino acid disorders: postmortem diagnosis of inborn errors of amino acid metabolism. Tada K; Yoshida T; Arakawa T Tohoku J Exp Med; 1970 Jul; 101(3):223-6. PubMed ID: 5455854 [No Abstract] [Full Text] [Related]
15. Phenylketonuria and other phenylalaninaemias. Blaskovics ME Clin Endocrinol Metab; 1974 Mar; 3(1):87-105. PubMed ID: 4609651 [No Abstract] [Full Text] [Related]
16. 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]
17. [Hereditary amino acid metabolism disorders. Indications for early diagnosis]. Kroll S; Zebisch P; Toussaint W Fortschr Med; 1972 Apr; 90(11):423-8. PubMed ID: 4680607 [No Abstract] [Full Text] [Related]
18. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies]. Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972 [No Abstract] [Full Text] [Related]
20. [5 years of the Austrian program for the early detection of inborn errors of metabolism. Activity report]. Thalhammer O; Scheibenreiter S; Schön R; Knoll E; Schmierer G Wien Klin Wochenschr; 1972; 84():Suppl 2:3-12. PubMed ID: 5085466 [No Abstract] [Full Text] [Related] [Next] [New Search]