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2. Excretion of hippuric acid during sodium benzoate therapy in patients with hyperglycinaemia or hyperammonaemia. Barshop BA; Breuer J; Holm J; Leslie J; Nyhan WL J Inherit Metab Dis; 1989; 12(1):72-9. PubMed ID: 2501586 [TBL] [Abstract][Full Text] [Related]
3. Use of placental enzyme analysis in assessment of the newborn at risk for non-ketotic hyperglycinaemia (NKH). Toone JR; Applegarth DA J Inherit Metab Dis; 1989; 12(3):281-5. PubMed ID: 2515368 [TBL] [Abstract][Full Text] [Related]
4. 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]
8. Non-ketotic hyperglycinaemia: prenatal diagnosis and detection of heterozygotes with glycine/serine ratios. Jordá A; Portolés M; Bonilla-Musoles F; Sweetman L; Nyhan WL J Inherit Metab Dis; 1987; 10(2):198-9. PubMed ID: 3116341 [No Abstract] [Full Text] [Related]
9. Clinical effects of serine medication in non-ketotic hyperglycinaemia due to deficiency of P-protein of the glycine cleavage complex. Wijburg FA; de Groot CJ; Schutgens RB; Barth PG; Tada K J Inherit Metab Dis; 1988; 11 Suppl 2():218-20. PubMed ID: 3141706 [No Abstract] [Full Text] [Related]
10. Molecular lesion of non-ketotic hyperglycinaemia. Tada K; Hayasaka K J Inherit Metab Dis; 1984; 7 Suppl 2():143-4. PubMed ID: 6434872 [No Abstract] [Full Text] [Related]
11. Evidence of defective threonine metabolism in non-ketotic hyperglycinaemia. Krieger I; Nigro M J Inherit Metab Dis; 1983; 6(1):40-3. PubMed ID: 6408308 [No Abstract] [Full Text] [Related]
12. Inherited metabolic disorders and seizures in infancy. De Vivo DC J Child Neurol; 2002 Dec; 17 Suppl 3():3S1-2. PubMed ID: 12597049 [No Abstract] [Full Text] [Related]