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62. FURTHER OBSERVATIONS OF A PATIENT WITH HYPERGLYCINEMIA. CHILDS B; NYHAN WL Pediatrics; 1964 Mar; 33():403-12. PubMed ID: 14129085 [No Abstract] [Full Text] [Related]
63. [Diagnosis of inborn amino acid metabolism errors. Important symptoms and laboratory methods]. Kroll S; Zebisch P; Toussaint W Fortschr Med; 1972 Apr; 90(11):430-1. PubMed ID: 4681731 [No Abstract] [Full Text] [Related]
64. Nonketotic hyperglycinemia. Okken A; de Groot CJ; Hommes FA J Pediatr; 1970 Jul; 77(1):164-5. PubMed ID: 5450279 [No Abstract] [Full Text] [Related]
65. [Progressive encephalopathy after a symptom-free period in the newborn infant, due to disorders of amino acid metabolism. Illustrated with case histories of patients with hyperglycinemia and maple syrup urine disease]. Raven EJ Ned Tijdschr Geneeskd; 1969 Oct; 113(42):1850-3. PubMed ID: 5344645 [No Abstract] [Full Text] [Related]
66. Hypervalinemia. Its metabolic lesion and therapeutic approach. Tada K; Wada Y; Arakawa T Am J Dis Child; 1967 Jan; 113(1):64-7. PubMed ID: 6066688 [No Abstract] [Full Text] [Related]
67. Nonketotic hyperglycinemia in a newborn infant. Tekinalp G; Coşkun T; Oran O; Ozalp I; Figen G; Ergin H Turk J Pediatr; 1995; 37(1):57-60. PubMed ID: 7732609 [TBL] [Abstract][Full Text] [Related]
68. Blindness due to non-ketotic hyperglycinemia: report of a 38-year-old, the oldest case to date. Tanaka Y; Miyazaki M; Tsuda M; Murai K; Kuzuhara S Intern Med; 1993 Aug; 32(8):641-2. PubMed ID: 8312663 [TBL] [Abstract][Full Text] [Related]
69. Studies on amino acid metabolism in citrullinuria. Mohyuddin F; Rathbun JC; McMurray WC Am J Dis Child; 1967 Jan; 113(1):152-6. PubMed ID: 6015893 [No Abstract] [Full Text] [Related]
70. Isovaleric acidemia: use of glycine therapy in neonates. Cohn RM; Yudkoff M; Rothman R; Segal S N Engl J Med; 1978 Nov; 299(18):996-9. PubMed ID: 692626 [No Abstract] [Full Text] [Related]
71. [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]
72. Congenital hyperammonemia. Association with hyperglycinemia and decreased levels of carbamyl phosphate synthetase. Freeman JM; Nicholson JF; Schimke RT; Rowland LP; Carter S Arch Neurol; 1970 Nov; 23(5):430-7. PubMed ID: 5471650 [No Abstract] [Full Text] [Related]
73. [A case of isovaleric acidemia]. Guibaud P; Divry P; Dubois Y; Collombel C; Larbre F Arch Fr Pediatr; 1973; 30(6):633-45. PubMed ID: 4805283 [No Abstract] [Full Text] [Related]
75. Non-ketotic hyperglycinemia: a case report. Singh M; Ghai OP Indian Pediatr; 1975 Feb; 12(2):197-9. PubMed ID: 1158480 [No Abstract] [Full Text] [Related]
76. Non-ketotic hyperglycinaemia in a neonate. A case report. De Ravel TJ; Smith CE; Scher LG; Davies VA; Rothberg AD S Afr Med J; 1991 Aug; 80(4):201-2. PubMed ID: 1876959 [TBL] [Abstract][Full Text] [Related]
77. Metabolism of glycine in the nonketotic form of hyperglycinemia. Ando T; Nyhan WL; Gerritsen T; Gong L; Heiner DC; Bray PF Pediatr Res; 1968 Jul; 2(4):254-63. PubMed ID: 5669662 [No Abstract] [Full Text] [Related]
78. A defect in branched-chain amino acid metabolism in a patient with congenital lactic acidosis due to dihydrolipoyl dehydrogenase deficiency. Taylor J; Robinson BH; Sherwood WG Pediatr Res; 1978 Jan; 12(1):60-2. PubMed ID: 643378 [TBL] [Abstract][Full Text] [Related]
79. 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: an X-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease. Perez-Cerda C; García-Villoria J; Ofman R; Sala PR; Merinero B; Ramos J; García-Silva MT; Beseler B; Dalmau J; Wanders RJ; Ugarte M; Ribes A Pediatr Res; 2005 Sep; 58(3):488-91. PubMed ID: 16148061 [TBL] [Abstract][Full Text] [Related]