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14 in total

1. [Clinical and molecular genetic characteristics of nonketotic hyperglycinemia].

Authors: Hai-Feng Li
Journal: Zhongguo Dang Dai Er Ke Za Zhi Date: 2017-03

2. Paracetamol prevents hyperglycinemia in vervet monkeys treated with valproate.

Authors: Jacques Viljoen; Jakobus J Bergh; Lodewyk J Mienie; Hercullas F Kotze; Gisella Terre'Blanche
Journal: Metab Brain Dis Date: 2012-02-17 Impact factor: 3.584

3. Perioperative care of a child with non-ketotic hyperglycinemia.

Authors: Joy Allee; Joseph D Tobias
Journal: Saudi J Anaesth Date: 2010-09

4. Interpretation of plasma amino acids in the follow-up of patients: the impact of compartmentation.

Authors: Claude Bachmann
Journal: J Inherit Metab Dis Date: 2008-01-31 Impact factor: 4.982

5. Musculoskeletal manifestations of neonatal nonketotic hyperglycinemia.

Authors: Norman Ramirez; John M Flynn; Francisco Casalduc; Stephanie Rodriguez; Alberto S Cornier; Simón Carlo
Journal: J Child Orthop Date: 2012-05-25 Impact factor: 1.548

6. Glycine decarboxylase deficiency-induced motor dysfunction in zebrafish is rescued by counterbalancing glycine synaptic level.

Authors: Raphaëlle Riché; Meijiang Liao; Izabella A Pena; Kit-Yi Leung; Nathalie Lepage; Nicolas DE Greene; Kyriakie Sarafoglou; Lisa A Schimmenti; Pierre Drapeau; Éric Samarut
Journal: JCI Insight Date: 2018-11-02

Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia).

1. [Clinical and molecular genetic characteristics of nonketotic hyperglycinemia].

2. Paracetamol prevents hyperglycinemia in vervet monkeys treated with valproate.

3. Perioperative care of a child with non-ketotic hyperglycinemia.

4. Interpretation of plasma amino acids in the follow-up of patients: the impact of compartmentation.

5. Musculoskeletal manifestations of neonatal nonketotic hyperglycinemia.

6. Glycine decarboxylase deficiency-induced motor dysfunction in zebrafish is rescued by counterbalancing glycine synaptic level.

7. Sequential magnetic resonance spectroscopic changes in a patient with nonketotic hyperglycinemia.

8. Genotypic and phenotypic features in Turkish patients with classic nonketotic hyperglycinemia.

9. Attenuated form of Glycine Encephalopathy: An Unusual Cause of Neurodevelopmental Disorder.

10. The relation of cerebrospinal fluid and plasma glycine levels in propionic acidaemia, a 'ketotic hyperglycinaemia'.