Disorders of Glycine Metabolism
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-67727-5_26
Reference25 articles.
1. Aburahma S, Khassawneh M, Griebel M, Sharp G, Gibson J. Pitfalls in measuring cerebrospinal fluid glycine levels in infants with encephalopathy. J Child Neurol. 2011;26:703–6.
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3. Alfallaj R, Alfadhel M. Glycine transporter 1 encephalopathy from biochemical Pathway to clinical disease: review. Child Neurol Open. 2019;6:2329048X19831486.
4. Aliefendioğlu D, Aslan AT, Coşkun T, Dursun A, Çakmak FN, Keismer M. Transient nonketotic hyperglycinemia: two case reports and literature review. Pediatr Neurol. 2003;28:151–5.
5. Applegarth DA, Toone JR, Rolland MO, Black SH, Yim DK, Bemis G. Non-concordance of CVS and liver glycine cleavage enzyme in three families with non-ketotic hyperglycinemia (NKH) leading to false negative prenatal diagnoses. Prenat Diagn. 2000;20:367–70.
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