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26. Screening tests and chromatography for the detection of inborn errors of metabolism. Stuber A. Clin Chim Acta; 1972 Feb; 36(2):309-13. PubMed ID: 5008795 [No Abstract] [Full Text] [Related]
27. [Aminoaciduria and aminoacidemia in spinal muscular atrophy]. Górecka A. Neurol Neurochir Pol; 1969 Feb; 3(5):607-12. PubMed ID: 5360553 [No Abstract] [Full Text] [Related]
28. Tyrosinemia with plantar and palmar keratosis and keratitis. Goldsmith LA, Kang E, Bienfang DC, Jimbow K, Gerald P, Baden HP. J Pediatr; 1973 Nov; 83(5):798-805. PubMed ID: 4270265 [No Abstract] [Full Text] [Related]
29. [URINARY ELIMINATION OF THE METABOLITES OF TRYPTOPHAN IN NEUROLOGICAL DISEASES IN CHILDREN. 1. RESULTS IN HYPSARRHYTHMIA, EPILEPSY AND MENTAL RETARDATION WITHOUT CONVULSIONS]. FOIS A, LECCHINI L. Riv Clin Pediatr; 1963 Oct; 72():182-95. PubMed ID: 14136000 [No Abstract] [Full Text] [Related]
34. The Vodskov Project VII: the amino acids in plasma and urine determined by ion exchange chromatography in a selected patient material and in a normal material. Espersen O, Paaby P. Dan Med Bull; 1971 Aug; 18(4):88-99. PubMed ID: 5570689 [No Abstract] [Full Text] [Related]
39. Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients. Kekomäki M, Visakorpi JK, Perheentupa J, Saxén L. Acta Paediatr Scand; 1967 Nov 14; 56(6):617-30. PubMed ID: 6076999 [No Abstract] [Full Text] [Related]
40. Aminoaciduria in epilepsy. CHOREMIS C, KYRIAKIDES V, KARPOUZAS J. J Pediatr; 1959 Nov 14; 55():593-601. PubMed ID: 13810005 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]