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Atrophia gyrata mit Makuladystrophie = Atrophie gyrata avec dystrophie maculaire = Atrophia gyrata with macular dystrophyHENNEKES, R; GERDING, H.Klinische Monatsblätter für Augenheilkunde. 1985, Vol 187, Num 3, pp 216-218, issn 0023-2165Article

ULTRASTRUCTURE OF HEPATIC MITOCHONDRIA IN A CHILD WITH HYPERORNITHINEMIA, HYPERAMMONEMIA, AND HEMOCITRULLINURIAHAUST DM; GATFIELD PD; GORDON BA et al.1981; HUM. PATHOL.; ISSN 0046-8177; USA; DA. 1981; VOL. 12; NO 3; PP. 212-223; BIBL. 49 REF.Article

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DEFECTIVE ORNITHINE METABOLISM IN THE SYNDROME OF HYPERORNITHINAEMIA, HYPERAMMONAEMIA AND HOMOCITRULLINURIASHIH VE; MANDELL R; HERZFELD A et al.1981; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1981; VOL. 4; NO 2; PP. 95-96; BIBL. 9 REF.Article

LYSINE IN TREATMENT OF HYPERORNITHINEMIAGIORDANO C; DESANTO NG; PLUVIO M et al.1978; NEPHRON; CHE; DA. 1978; VOL. 22; NO 1-3; PP. 97-106; BIBL. 19 REF.Article

HYPERORNITHINAEMIA AND GYRATE ATROPHY OF THE RETINA: IMPROVEMENT OF VISION DURING TREATMENT WITH A LOW-ARGININE DIETMCINNES RR; ARSHINOFF SA; BELL L et al.1981; LANCET (BR. ED.); ISSN 0140-6736; GBR; DA. 1981; VOL. 1; NO 8219; PP. 513-517; BIBL. 15 REF.Article

DEFICIENT L-ORNITHINE: 2-OXOACID AMINOTRANSFERASE ACTIVITY IN CULTURED FIBROBLASTS FROM A PATIENT WITH GYRATE ATROPHY OF THE RETINA.O'DONNELL JJ; SANDMAN RP; MARTIN SR et al.1977; BIOCHEM. BIOPHYS. RES. COMMUNIC.; U.S.A.; DA. 1977; VOL. 79; NO 2; PP. 396-399; BIBL. 12 REF.Article

The pH of mitochondria of fibroblasts from a hypernithinaemia, hyperammonaemia homocitrullinaria-syndrome patientMETOKI, K; HOMMES, G. F. A.Journal of inherited metabolic disease. 1984, Vol 7, Num 1, pp 9-11, issn 0141-8955Article

CLINICAL AND BIOCHEMICAL HETEROGENEITY IN GYRATE ATROPHYKAISER KUPFER MI; VALLE D; BRON AJ et al.1980; AMER. J. OPHTHALMOL.; USA; DA. 1980; VOL. 89; NO 2; PP. 219-222; BIBL. 11 REF.Article

METABOLIC STUDIES IN TWO FAMILIES WITH HYPERORNITHINEMIA AND GYRATE ATROPHY OF CHOROID AND RETINAYATZIV S; STATTER M; MERIN S et al.1979; J. LAB. CLIN. MED.; USA; DA. 1979; VOL. 93; NO 5; PP. 749-757; BIBL. 18 REF.Article

ORNITHINE KETOACID TRANSAMINASE DEFICIENCY IN GYRATE ATROPHY OF THE CHOROID AND RETINA.SHIH VE; BERSON EL; MANDELL R et al.1978; AMER. J. HUM. GENET.; U.S.A.; DA. 1978; VOL. 30; NO 2; PP. 174-179; BIBL. 20 REF.Article

INHIBITION OF ARGININE-GLYCINE AMIDINOTRANSFERASE BY ORNITHINE: A POSSIBLE MECHANISM FOR THE MUSCULAR AND CHORIORETINAL ATROPHIES IN GYRATE ATROPHY OF THE CHOROID AND RETINA WITH HYPERORNITHINEMIASIPILA I.1980; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1980; VOL. 613; NO 1; PP. 79-84; BIBL. 20 REF.Article

GYRATE ATROPHY OF CHOROID ASSOCIATED WITH HYPERORNITHINAEMIA: REPORT OF THE FIRST CASE IN ITALYRINALDI E; STOPPOLONI GP; SAVASTANO S et al.1979; J. PEDIATR. OPHTHALMOL. STRABISM.; USA; DA. 1979; VOL. 16; NO 2; PP. 132-135; BIBL. 7 REF.Article

ORNITHINE METHYL ESTER. AN UNUSUAL METABOLITE ENCOUNTERED IN THE URINE OF PATIENTS WITH A UREA CYCLE DISORDER CHARACTERIZED BY HYPERAMMONEMIA HYPERORNITHINEMIA AND HOMOCITRULLINURIA.GORDON BA; GATFIELD PD; TALLER E et al.1977; CLIN. BIOCHEM.; CANADA; DA. 1977; VOL. 10; NO 2; PP. 78-82; BIBL. 23 REF.Article

Neonatal onset of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome with favorable outcomeZAMMARCHI, E; CIANI, F; PASQUINI, E et al.The Journal of pediatrics. 1997, Vol 131, Num 3, pp 440-443, issn 0022-3476Article

Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome : neurologic, ophthalmologic, and neuropsychologic examination of six patientsLEMAY, J. F; LAMBERT, M. A; ORQUIN, J et al.The Journal of pediatrics. 1992, Vol 121, Num 5, pp 725-730, issn 0022-3476, 1Article

Das H-H-H-Syndrom: eine seltene, auch anästhesiologisch relevante Erkrankung = Le syndrome H-H-H (hyperornithinémie, hyperammoniémie homocitrullinurie): une maladie rare à incidence anesthésique = H-H-H syndrome: a rare disease with importance in anaesthesiaMICHAELIS, G; BISCOPING, J; HEMPELMANN, G et al.Anästhesie, Intensivtherapie, Notfallmedizin. 1986, Vol 21, Num 6, pp 315-317, issn 0174-1837Article

Free amino acid concentration in blood cells of two brothers with gyrate atrophy of the choroid and retina with hyperornithinaemiaFUKUDA, K; NISHI, Y; USUI, T et al.Journal of inherited metabolic disease. 1983, Vol 6, Num 4, pp 137-142, issn 0141-8955Article

CONTACT DERMATITIS TO NICKEL AND EARLY CATARACT IN TWO SISTERS WITH HYPERORNITHINEMIAGARCIA PEREZ A; MARTIN PASCUAL A; FRANCO A et al.1981; CONTACT DERMAT.; DNK; DA. 1981; VOL. 7; NO 2; PP. 123; BIBL. 3 REF.Article

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A new family affected by the syndrome of hyperornithinaemia, hyperammonaemia and homocitrullinuriaRODES, M; RIBES, A; PINEDA, M et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 1, pp 73-81, issn 0141-8955Article