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kw.\*:("Hyperglycinémie")

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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

STUDIES ON THE VALINE SENSITIVITY IN NON-KETOTIC HYPERGLYCINEMIA. = LES ETUDES SUR LA SENSIBILITE A LA VALINE DANS L'HYPERGLYCINEMIE NON CETOSIQUEDE GROOT CJ; VAN DEN BERG H; HOMMES FA et al.1975; HELV. PAEDIATR. ACTA; SUISSE; DA. 1975; VOL. 30; NO 3; PP. 247-254; ABS. ALLEM. FR.; BIBL. 10 REF.Article

A BLOCK IN GLYCINE CLEAVAGE REACTION AS A COMMON MECHANISM IN KETOTIC AND NONKETOTIC HYPERGLYCINEMIA = UN BLOC DANS LA REACTION DE CLIVAGE DE LA GLYCINE COMME MECANISME COMMUN DANS L'HYPERGLYCINEMIE CETOSIQUE ET NON CETOSIQUETADA K; CORBEEL LM; EECKELS R et al.1974; PEDIATR. RES.; U.S.A.; DA. 1974; VOL. 8; NO 7; PP. 721-723; BIBL. 15REF.Article

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

NON-KETOTIC HYPERGLYCINEMIA: A CASE REPORTMEHARBAN SINGH; GHAI OP.1975; INDIAN PEDIATR.; INDIA; DA. 1975; VOL. 12; NO 2; PP. 197-199; BIBL. 7REF.Article

INTERPRETATION OF ELEVATED BLOOD GLYCINE LEVELS IN CHILDREN. = INTERPRETATION DE L'ELEVATION DU TAUX SANGUIN DE GLYCINE CHEZ LES ENFANTSAPPLEGARTH DA; POON S.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 63; NO 1; PP. 49-54; BIBL. 13 REF.Article

A survey on prenatal diagnosis of inherited metabolic diseases in JapanTADA, K; AIKAWA, J; IGARASHI, Y et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 260-262, issn 0141-8955, suppl. 2Article

Use of placental enzyme analysis in assessment of the newborn at risk for non-ketotic hyperglycinaemia (NKH)TOONE, J. R; APPLEGARTH, D. A.Journal of inherited metabolic disease. 1989, Vol 12, Num 3, pp 281-285, issn 0141-8955Article

Non-ketotic hyperglycinaemia : molecular lesion, diagnosis and pathophysiologyTADA, K; KURE, S.Journal of inherited metabolic disease. 1993, Vol 16, Num 4, pp 691-703, issn 0141-8955Conference Paper

L'HYPERGLYCINEMIE SANS CETOSE CONGENITALE. UNE NOUVELLE OBSERVATIONPIUSSAN C; SAUDUBRAY JM; VAN POPERINGHE M et al.1975; PEDIATRIE; FR.; DA. 1975; VOL. 30; NO 4; PP. 429-431Article

HYPERGLYCINEMIEHYANEK J; POSPISIL R; HOZA J et al.1975; CESKOSL. PEDIATR.; CESKOSL.; DA. 1975; VOL. 30; NO 11; PP. 543-545; ABS. RUSSE ANGL.; BIBL. 7 REF.Article

INHIBITION OF GLYCINE SERINE INTERCONVERSION IN CULTURED HUMAN FIBROBLASTS BY PRODUCTS OF ISOLEUCINE CATABOLISM = INHIBITION PAR LES PRODUITS DU CATABOLISME DE L'ISOLEUCINE DE L'INTERCONVERSION GLYCINE-SERINE DANS LES FIBROBLASTES HUMAINS EN CULTUREHILLMAN RE; OTTO EF.1974; PEDIATR. RES.; U.S.A.; DA. 1974; VOL. 8; NO 12; PP. 941-945; BIBL. 19REF.Article

NONKETOTIC HYPERGLYCINEMIA. GLYCINE ACCUMULATION DUE TO ABSENCE OF GLYCINE CLEAVAGE IN BRAIN. = HYPERGLYCINEMIE NON CETONIQUE. ACCUMULATION DE GLYCINE DUE A L'ABSENCE DE CLIVAGE DE LA GLYCINE DANS L'ENCEPHALEPERRY TL; URQUHART N; MAC LEAN J et al.1975; NEW ENGL. J. MED.; U.S.A.; DA. 1975; VOL. 292; NO 24; PP. 1269-1273; BIBL. 21 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

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

THE VITAMIN B12-DEFICIENT RAT AS A POSSIBLE MODEL OF KETOTIC HYPERGLYCINEMIA. = LE RAT CARENCE EN VITAMINE B12, MODELE POSSIBLE DE L'HYPERGLYCINEMIE CETOSIQUEO'NEILL ROWLEY B; BROTHERS V; GERRITSEN T et al.1975; PEDIATR. RES.; U.S.A.; DA. 1975; VOL. 9; NO 10; PP. 782-786; BIBL. 41 REF.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

METHYLMALONIC ACIDAEMIA AND NONKETOTIC HYPERGLYCINAEMIA: CLINICAL AND BIOCHEMICAL ASPECTS = ACIDEMIE METHYLMALONIQUE ET HYPERGLYCINEMIE NON CETOSIQUE: ASPECTS CLINIQUES ET BIOCHIMIQUESCORBEEL L; TADA K; COLOMBO JP et al.1975; ARCH. DIS. CHILDH.; G.B.; DA. 1975; VOL. 50; NO 2; PP. 103-109; BIBL. 31REF.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

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