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kw.\*:("Hyperglycinemia")

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Nonketotic hyperglycinemia: two patients with primary defects of P-protein and T-protein, respectively, in the glycine cleavage systemHAYASAKA, K; TADA, K; KIKUCHI, G et al.Pediatric research. 1983, Vol 17, Num 12, pp 967-970, issn 0031-3998Article

Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical casesHAYASAKA, K; TADA, K; SCHUTGENS, R. B. H et al.The Journal of pediatrics. 1987, Vol 110, Num 6, pp 873-877, issn 0022-3476Article

Nonketotic hyperglycinemia: Diffusion magnetic resonance imaging findingsSENER, R. Nuri.Journal of computer assisted tomography. 2003, Vol 27, Num 4, pp 538-540, issn 0363-8715, 3 p.Article

Neonatal Nonketotic HyperglycinemiaBHAMKAR, Rahul P; COLACO, Prisca.Indian journal of pediatrics. 2007, Vol 74, Num 12, pp 1124-1126, issn 0019-5456, 3 p.Article

GLYCINE TRANSPORT BY HUMAN DIPLOID FIBROBLASTS. ABSENCE OF A DEFECT IN CELLS FROM PATIENTS WITH NONKETOTIC HYPERGLYCINEMIAKELLY JC; OTTO EF; HILLMAN RE et al.1979; PEDIATR. RES.; USA; DA. 1979; VOL. 13; NO 2; PP. 127-130; BIBL. 30 REF.Article

Neonatal non-ketotic hyperglycinemia (NKH): diagnoses and management in two casesHOLMQVIST, P; POLBERGER, S.Neuropediatrics. 1985, Vol 16, Num 4, pp 191-193, issn 0174-304XArticle

A Known and a Novel Mutation in the Glycine Decarboxylase Gene in a Newborn with Classic Nonketotic HyperglycinemiaBEIJER, P; LICHTENBELT, K. D; HOFSTEDE, F. C et al.Neuropediatrics. 2012, Vol 43, Num 3, pp 164-167, issn 0174-304X, 4 p.Article

Proteomic analysis in cerebrospinal fluid of patients with atypical nonketotic hyperglycinemia and pulmonary hypertension: A pilot studyRODRIGUEZ, Carlos E; ARRANZ, José A; COLOME, Nuria et al.Proteomics. Clinical applications (Print). 2009, Vol 3, Num 12, pp 1430-1439, issn 1862-8346, 10 p.Article

Failure of early diazepam treatment in a neonate with non-ketotic hyperglycinaemiaAUKETT, A; BRAITHWAITE, R. A; GREEN, A et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 268-271, issn 0141-8955, suppl. 2Conference Paper

L'encéphalopathie à la glycine. Une observation. Echec du sulfate de strychnine = Glycine encephalopathy (concerning are case: unsuccessful treatment by strychnine sulfate)VITTU, G; LAMBLIN, D; PRUVOT, P et al.LARC médical. 1985, Vol 5, Num 7, pp 387-389, issn 0242-9462Article

Nonketotic hyperglycinemia presenting with pin-point pupils and hyperammonemiaSCHIFFMANN, R; BONEH, A; ERGAZ, Z et al.Israel journal of medical sciences. 1992, Vol 28, Num 2, pp 91-93, issn 0021-2180Article

Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia: observations on sisters with a mild T-protein defectHAAN, E. A; KIRBY, D. M; TADA, K et al.European journal of pediatrics. 1986, Vol 145, Num 4, pp 267-270, issn 0340-6199Article

Floppy eyelid with hyperglycinemiaGERNER, E. W; HUGHES, S. M.American journal of ophthalmology. 1984, Vol 98, Num 15, pp 614-616, issn 0002-9394Article

LEUKOCYTE PROPIONYL-COA CARBOXYLASE DEFICIENCY IN A PATIENT WITH KETOTIC HYPERGLYCINAEMIADEL VALLE JA; MERINERO B; GARCIA MJ et al.1980; J. INHERIT. METAB. DIS.; GBR; DA. 1980; VOL. 3; NO 3; PP. 93; BIBL. 4 REF.Article

NONKETOTIC HYPERGLYCINEMIA: A GENETIC STUDY OF 13 FINNISH FAMILIESWENDT LV; HIRVASNIEMI A; SIMILA S et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 5; PP. 411-417; BIBL. 27 REF.Article

METABOLISM OF GLYCINE IN THE NORMAL INDIVIDUAL AND IN PATIENTS WITH NON-KETOTIC HYPERGLYCINAEMIANYHAN WL.1982; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 2; PP. 105-110; BIBL. 2 P.Article

NON-KETOTIC HYPERGLYCINAEMIA - A REVIEW OF 70 PATIENTSCARSON NAJ.1982; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 2; PP. 126-128; BIBL. 2 REF.Article

PROGRESSIVE NEURODEGENERATIVE DISORDER IN A PATIENT WITH NONKETOTIC HYPERGLYCINEMIATRAUNER DA; PAGE T; GRECO C et al.1981; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1981; VOL. 98; NO 2; PP. 272-275; BIBL. 11 REF.Article

MEGALOCORNEA IN NONKETOTIC HYPERGLYCINEMIAHOYT CS; BROWN RA.1978; J. PEDIATR. OPHTHALMOL. STRABISM.; USA; DA. 1978; VOL. 15; NO 2; PP. 85-88; BIBL. 27 REF.Article

D-GLYCERIC-ACIDAEMIA AND NON-KETOTIC HYPERGLYCINAEMIA.BRANDT NJ; RASMUSSEN K; BRANDT S et al.1976; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1976; VOL. 65; NO 1; PP. 17-22; BIBL. 19 REF.Article

Variant non-ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5BAKER, Peter R; FRIEDERICH, Marisa W; LEE, Wang-Tso et al.Brain. 2014, Vol 137, pp 366-379, issn 0006-8950, 14 p., 2Article

A decrease in glycine cleavage activity in the liver of a patient dihydrolipoyl dehydrogenase deficiencyYOSHINO, M; KOGA, Y; YAMASHITA, F et al.Journal of inherited metabolic disease. 1986, Vol 9, Num 4, pp 399-400, issn 0141-8955Article

The effectiveness of benzoate in the management of seizures in nonketotic hyperglycinemiaWOLFF, J. A; KULOVICH, S; YU, A. L et al.American journal of diseases of children (1960). 1986, Vol 140, Num 6, pp 596-602, issn 0002-922XArticle

Treatment from birth of nonketotic hyperglycinemia due to a novel GLDC mutationKORMAN, Stanley H; WEXLER, Isaiah D; GUTMAN, Alisa et al.Annals of neurology. 2006, Vol 59, Num 2, pp 411-415, issn 0364-5134, 5 p.Article

Natural history of nonketotic hyperglycinemia in 65 patientsHOOVER-FONG, J. E; SHAH, S; VAN HOVE, J. L. K et al.Neurology. 2004, Vol 63, Num 10, pp 1847-1853, issn 0028-3878, 7 p.Article

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