Bhumika S, M Basalingappa K, Gopenath T, Basavaraju S
Egypt J Neurol Psychiatr Neurosurg. 2022; 58(1):132.
PMID: 36415754
PMC: 9672649.
DOI: 10.1186/s41983-022-00567-6.
Manoli I, Pass A, Harrington E, Sloan J, Gagne J, McCoy S
Genet Med. 2021; 23(8):1522-1533.
PMID: 33820958
PMC: 8354855.
DOI: 10.1038/s41436-021-01143-8.
Reijngoud D
J Inherit Metab Dis. 2018; 41(3):309-328.
PMID: 29318410
PMC: 5959979.
DOI: 10.1007/s10545-017-0124-5.
Rosario P, Medina J
J Inherit Metab Dis. 1982; 5(1):59-62.
PMID: 6820416
DOI: 10.1007/BF01799756.
Ugarte M, Garcia M, Benavides J, Valdivieso F
J Inherit Metab Dis. 1980; 2(4):93-9.
PMID: 6796767
DOI: 10.1007/BF01805665.
Threonine dehydratase deficiency: a probable cause of non-ketotic hyperglycinaemia.
Krieger I, Booth F
J Inherit Metab Dis. 1984; 7(2):53-6.
PMID: 6434824
DOI: 10.1007/BF01805800.
Evidence of defective threonine metabolism in non-ketotic hyperglycinaemia.
Krieger I, Nigro M
J Inherit Metab Dis. 1983; 6(1):40-3.
PMID: 6408308
DOI: 10.1007/BF02391192.
The clinical findings in a patient with nonketotic hyperglycinemia.
REPLOH H, Grobe H, DIEKMANN L, Palm D, von Bassewitz D, Jenett W
Z Kinderheilkd. 1973; 114(3):191-204.
PMID: 4723704
DOI: 10.1007/BF00497423.
3-hydroxypropionate: significance of -oxidation of propionate in patients with propionic acidemia and methylmalonic acidemia.
Ando T, Rasmussen K, Nyhan W, Hull D
Proc Natl Acad Sci U S A. 1972; 69(10):2807-11.
PMID: 4507604
PMC: 389649.
DOI: 10.1073/pnas.69.10.2807.
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.
Coude F, Sweetman L, Nyhan W
J Clin Invest. 1979; 64(6):1544-51.
PMID: 500823
PMC: 371306.
DOI: 10.1172/JCI109614.
Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.
Corbeel L, Tada K, COLOMBO J, EECKELS R, Eggermont E, Jaeken J
Arch Dis Child. 1975; 50(2):103-9.
PMID: 236734
PMC: 1544395.
DOI: 10.1136/adc.50.2.103.
Non-ketotic hyperglycinaemia in a family with an unusual phenotype.
Ando T, Nyhan W, Bicknell J, Harris R, Stern J
J Inherit Metab Dis. 1978; 1(3):79-83.
PMID: 116082
DOI: 10.1007/BF01805677.
