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2. Dietary management of inborn errors of amino acid metabolism. O'Brien D Postgrad Med; 1979 Apr; 65(4):133-8. PubMed ID: 424346 [TBL] [Abstract][Full Text] [Related]
3. [The cofactor correlation. The metabolic block and its treatment]. Paluszak J Pol Arch Med Wewn; 1974 Nov; 52(5):531-9. PubMed ID: 4139696 [No Abstract] [Full Text] [Related]
4. [Development of domestic products for the treatment of hereditary disorders of amino acid metabolism]. Simůnek Z; Blattná J; Puzejová M Cesk Pediatr; 1980; 35(2):55-6. PubMed ID: 7371096 [No Abstract] [Full Text] [Related]
5. [Diseases due to enzyme defects in childhood. Nosography and recent progress]. Panizon F Quad Sclavo Diagn; 1971 Mar; 7(1):44-80. PubMed ID: 4344048 [No Abstract] [Full Text] [Related]
6. Diet therapy for inborn errors of amino acid metabolism. Efron ML J Am Diet Assoc; 1967 Jul; 51(1):40-5. PubMed ID: 6027632 [No Abstract] [Full Text] [Related]
7. [Use of protein supplements in diet therapy of phenylketonuria and other hereditary amino acid metabolism disorders]. Hyánek J; Viletová H; Simová O; Dusek V; Simková M; Hoza J Cesk Pediatr; 1980; 35(2):53-4. PubMed ID: 7371095 [No Abstract] [Full Text] [Related]
8. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase. Sunshine P; Lindenbaum JE; Levy HL; Freeman JM Pediatrics; 1972 Jul; 50(1):100-11. PubMed ID: 5038084 [No Abstract] [Full Text] [Related]
9. [Recent developments in amino-acidopathies]. Farriaux JP Lille Med; 1971 Feb; 16(2):342-55. PubMed ID: 5575812 [No Abstract] [Full Text] [Related]
10. Vitamin B12-dependent methylmalonicaciduria: amino acid toxicity, long chain ketonuria, and protective effect of vitamin B12. Hsia YE; Lilljeqvist AC; Rosenberg LE Pediatrics; 1970 Oct; 46(4):497-507. PubMed ID: 5503685 [No Abstract] [Full Text] [Related]
15. New approaches to the diagnosis and treatment of inborn errors or urea synthesis. Batshaw ML; Thomas GH; Brusilow SW Pediatrics; 1981 Aug; 68(2):290-7. PubMed ID: 7267240 [No Abstract] [Full Text] [Related]
16. New trends in the treatment of inborn errors of metabolism: an overview. Frézal J; Munnich A; Ogier H; Weil D; Saudubray JM Prog Clin Biol Res; 1982; 103 Pt B():563-71. PubMed ID: 7163247 [No Abstract] [Full Text] [Related]
17. Newer trends in the genetic and biochemical studies in the etiopathogenesis of aminoacidopathies. Nair KR; Virmani V Neurol India; 1973 Sep; 21(3):128-36. PubMed ID: 4784816 [No Abstract] [Full Text] [Related]
18. Protein and essential amino acid requirements in a child with propionic acidemia. Queen PM; Fernhoff PM; Acosta PB J Am Diet Assoc; 1981 Nov; 79(5):562-5. PubMed ID: 7288063 [No Abstract] [Full Text] [Related]
19. Advantages of supplementary alanine in infants with genetic defects of amino acid metabolism. Nutr Rev; 1986 May; 44(5):164-6. PubMed ID: 3523316 [No Abstract] [Full Text] [Related]
20. Studies on requirements for amino acids in infants with disorders of amino acid metabolism. I. Effect of alanine. Kelts DG; Ney D; Bay C; Saudubray JM; Nyhan WL Pediatr Res; 1985 Jan; 19(1):86-91. PubMed ID: 3969320 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]