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Hereditary tyrosinemia: formation of succinylacetone ― Amino acid adductsMANABE, S; SASSA, S; KAPPAS, A et al.The Journal of experimental medicine. 1985, Vol 162, Num 3, pp 1060-1074, issn 0022-1007Article

A propos de deux cas de tyrosinose de type II (syndrome de Richner-Hanhart) = About two cases of tyrosinosis II (Richner-Hanhart syndrome)ROUSSAT, B; FOURNIER, F; BESSON, D et al.Bulletin des sociétés d'ophtalmologie de France. 1988, Vol 88, Num 6-7, pp 751-757, issn 0081-1270Article

Visceral pathology of hereditary tyrosinemia type IRUSSO, P; O'REGAN, S.American journal of human genetics. 1990, Vol 47, Num 2, pp 317-324, issn 0002-9297, 8 p.Article

Hereditary tyrosinemia type I: an overviewKVITTINGEN, E. A.Scandinavian journal of clinical & laboratory investigation. Supplement. 1986, Vol 46, Num 184, pp 27-34, issn 0085-591XArticle

Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)TANGUAY, R. M; VALET, J. P; LESCAULT, A et al.American journal of human genetics. 1990, Vol 47, Num 2, pp 308-316, issn 0002-9297, 9 p.Article

Tyrosinaemia type II (Richner―Hanhart syndrome): report of two cases treated with etretinateFRASER, N. G; MACDONALD, J; GRIFFITHS, W. A. D et al.Clinical and experimental dermatology (Print). 1987, Vol 12, Num 6, pp 440-443, issn 0307-6938Article

The pre- and post-natal diagnosis of tyrosinemia type I and the detection of the carrier state by assay of fumarylacetoacetaseKVITTINGEN, E. A; BRODTKORB, E.Scandinavian journal of clinical & laboratory investigation. Supplement. 1986, Vol 46, Num 184, pp 35-40, issn 0085-591XArticle

Oral loading of homogentisic acid in controls and in obligate heterozygotes for hereditary tyrosinemia type ILABERGE, C; LESCAULT, A; GRENIER, A et al.American journal of human genetics. 1990, Vol 47, Num 2, pp 329-337, issn 0002-9297, 9 p.Article

Tyrosinemia II: a large North Carolina kindredGOLDSMITH, L. A.Archives of internal medicine (1960). 1985, Vol 145, Num 9, pp 1697-1700, issn 0003-9926Article

Clinical and laboratory observations : hematin therapy for the neurologic crisis of tyrosinemiaRANK, J. M; PASCUAL-LEONE, A; PAYNE, W et al.The Journal of pediatrics. 1991, Vol 118, Num 1, pp 136-139, issn 0022-3476Article

Effect of dietary treatment on the renal tubular function in a patient with hereditary tyrosinemiaSUZUKI, Y; KONDA, M; IMAI, I et al.International journal of pediatrics nephrology. 1987, Vol 8, Num 3, pp 171-176, issn 0391-6510Article

Animal models of tyrosinemiaNAKAMURA, Kimitoshi; TANAKA, Yasuhiko; MITSUBUCHI, Hiroshi et al.The Journal of nutrition. 2007, Vol 137, Num 6S, issn 0022-3166, S1556-S1560, SUP1Conference Paper

Tyrosinaemia : treatment and outcomeKVITTINGEN, E. A.Journal of inherited metabolic disease. 1995, Vol 18, Num 4, pp 375-379, issn 0141-8955Conference Paper

Treatment of hereditary tyrosinaemia type I by inhition of 4-hydroxyphenylpyruvate dioxygenaseLINDSTEDT, S; HOLME, E; LOCK, E. A et al.Lancet (British edition). 1992, Vol 340, Num 8823, pp 813-817, issn 0140-6736Article

Une cause rare d'hyperphénylalaninémie néonatale : la tyrosinémie de type I = Tyrosinemia I: a rare cause of neonatal hyperphenylalaninemiaSARLES, J; MAURIN, N; GIRAUD, F et al.Pédiatrie (Marseille). 1992, Vol 47, Num 12, pp 809-811, issn 0031-4021Article

Outcome in tyrosinaemia type IIBARR, D. G. D; KIRK, J. M; LAING, S. C et al.Archives of disease in childhood. 1991, Vol 66, Num 10, pp 1249-1250, issn 0003-9888Article

Genetic epidemiology of hereditary tyrosinemia in Quebec and in Saguenay-Lac-St-JeanDE BRAEKELEER, M; LAROCHELLE, J.American journal of human genetics. 1990, Vol 47, Num 2, pp 302-307, issn 0002-9297, 6 p.Article

New forms of hereditary tyrosinemia type II in mink: hepatic tyrosine aminotransferase defectCHRISTENSEN, K; HENRIKSEN, P; SØRENSEN, H et al.Hereditas (Landskrona). 1986, Vol 104, Num 2, pp 215-222, issn 0018-0661Article

Urinary excretion of N-acetyl amino acids in patients with some inborn errors of amino acid metabolismJELLUM, E; HORN, L; THORESEN, O et al.Scandinavian journal of clinical & laboratory investigation. Supplement. 1986, Vol 46, Num 184, pp 21-26, issn 0085-591XArticle

Type I hereditary tyrosinaemia : presentation of 11 casesCOSKUN, T; OZALP, I; KOCAK, N et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 5, pp 765-770, issn 0141-8955Article

Tyrosinemia IIGOLDSMITH, L. A.International journal of dermatology. 1985, Vol 24, Num 5, pp 293-294, issn 0011-9059Article

Ophthalmic follow-up of patients with tyrosinaemia type I on NTBCGISSEN, P; PREECE, M. A; WILLSHAW, H. A et al.Journal of inherited metabolic disease. 2003, Vol 26, Num 1, pp 13-16, issn 0141-8955, 4 p.Article

Succinylacetone effects on renal tubular phosphate metabolism : a model for experimental renal Fanconi syndromeROTH, K. S; CARTER, B. E; HIGGINS, E. S et al.Proceedings of the Society for Experimental Biology and Medicine. 1991, Vol 196, Num 4, pp 428-431, issn 0037-9727Article

Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice : a murine model for hereditary tyrosinaemia type IIIENDO, F; KATOH, H; MATSUDA, I et al.Journal of inherited metabolic disease. 1990, Vol 13, Num 5, pp 780-782, issn 0141-8955, 3 p.Article