ERHOEHTE TYROSINBLUTSPIEGEL BEI NEUGEBORENEN = LES TAUX ELEVES DE TYROSINE SERIQUE CHEZ LE NOUVEAU-NESCHOEN R; SCHMIERER G.1972; Z. KINDERHEILKDE; DTSCH.; DA. 1972; VOL. 113; NO 4; PP. 303-311; ABS. ANGL.; BIBL. 12REF.Serial Issue

TYROSINOSIS: A NEW VARIANTZALESKI WA; HILL A.1973; CANAD. MED. ASS. J.; CANADA; DA. 1973; VOL. 108; NO 4; PP. 477-484 (5P.); ABS. FR.; BIBL. 32REF.Serial Issue

TYROSINOSIS. = TYROSINOSEBAKKER HD; VAN SPRANG FJ.1976; NEDERL. T. GENEESKDE; NEDERL.; DA. 1976; VOL. 120; NO 22; PP. 944-951; ABS. ANGL.; BIBL. 1 P.Article

LEVELS OF TYROSINE AND TRYPTOPHAN IN THE PLASMA AND BRAIN OF SPONTANEOUSLY HYPERTENSIVE RATS = TAUX DE TYROSINE ET DE TRYTOPHANE DANS LE PLASMA ET LE CERVEAU DES RATS SPONTANEMENT HYPERTENDUSOSUMI Y; TANAKA C; TAKAORI S et al.1974; JAP. J. PHARMACOL.; JAP.; DA. 1974; VOL. 24; NO 5; PP. 715-720; BIBL. 21REF.Article

Presentation of the data of the italian registry for oculocutaneous tyrosinaemiaFOIS, A; BORGOGNI, P; ROMANO, C et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 262-264, issn 0141-8955, suppl. 2Conference Paper

HAWKINSINURIA: A DOMINANTLY INHERITED DEFECT OF TYROSINE METABOLISM WITH SEVERE EFFECTS IN INFANCYWILCKEN B; HAMMOND JW; HOWARD N et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 305; NO 15; PP. 865-869; BIBL. 17 REF.Article

TYROSINEMIE HEREDITAIRE: EXAMEN DU FOIE EN MICROSCOPIE ELECTRONIQUE DE BIOPSIES HEPATIQUES: OBSERVATION DE 7 CAS.TREMBLAY M; BELANGER L; LAROCHELLE J et al.1977; REV. FR. GASTROENTEROL.; FR.; DA. 1977; NO 134; PP. 39-43; ABS. ANGL.; BIBL. 7 REF.Article

A NEW FORM OF PROLONGED TRANSIENT TYROSINEMIA PRESENTING WITH SEVERE METABOLIC ACIDOSIS = UNE NOUVELLE FORME DE TYROSINEMIE TRANSITOIRE PROLONGEE SE MANIFESTANT PAR UNE ACIDOSE METABOLIQUE GRAVEDANKS DM; TIPPETT P; ROGERS J et al.1975; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1975; VOL. 64; NO 2; PP. 209-214; BIBL. 20 REF.Article

GC-MS IDENTIFICATION OF URINARY SUCCINYLACETONE IN TWO CASES OF HEREDITARY TYROSINAEMIADIVRY P; ROLLAND MO; TESSIER J et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 1; PP. 41-42; BIBL. 8 REF.Article

A SYNDROME OF HEREDITARY TYROSINEMIA IN MINK (MUSTELA VISON SCHREB.)CHRISTENSEN K; FISCHER P; KNUDSEN KEB et al.1979; REV. CANAD. MED. COMP.; CAN; DA. 1979; VOL. 43; NO 3; PP. 333-340; ABS. FRE; BIBL. 24 REF.Article

TYROSINEMIE HEREDITAIRE: EXAMEN DU FOIE EN MICROSCOPIE ELECTRONIQUE DE BIOPSIES HEPATIQUES: OBSERVATION DE SEPT CASTREMBLAY M; BELANGER L; LAROCHELLE J et al.1978; REV. FR. GASTRO-ENTEROL.; FRA; DA. 1978; NO 144; PP. 17-21; ABS. ENG; BIBL. 7 REF.Article

Treatment of hereditary tyrosinaemia (fumarylacetoacetase deficiency) by enzyme substitutionLINDBLAD, B; FRIDEN, J; GRETER, J et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 257-261, issn 0141-8955, suppl. 2Conference Paper

Successfull dietary control of tyrosinemia IIMACHINO, H; MIKI, Y; KAWATSU, T et al.Journal of the American Academy of Dermatology. 1983, Vol 9, Num 4, pp 533-539, issn 0190-9622Article

Le traitement diététique de la tyrosinémie héréditaire: à propos de sept cas = Dietary management of hereditary tyrosinemiaJEHAN, P; BUCHMAN, M; ODIEVRE, M et al.La Semaine des hôpitaux de Paris. 1984, Vol 60, Num 20, pp 1412-1417, issn 0037-1777Article

DIETARY TREATMENT OF TYROSINEMIA TYPE IMICHALS K; MATALON R; WONG PWK et al.1978; J. AMER. DIET. ASS.; USA; DA. 1978; VOL. 73; NO 5; PP. 507-514; BIBL. 36 REF.Article

THE CHILD WITH AN UNUSUAL ODOR. A CLINICAL RESUMEMACE JW; GOODMAN SI; CENTERWALL WR et al.1976; CLIN. PEDIATR.; U.S.A.; DA. 1976; VOL. 15; NO 1; PP. 57-62; BIBL. 34 REF.Article

Persistent Tyrosinemia associated with low activity of tyrosine aminotransferaseANDERSSON, S; NEMETH, A; OHISALO, J et al.Pediatric research. 1984, Vol 18, Num 7, pp 675-678, issn 0031-3998Article

Tyrosinemia and intractable seizuresSESHIA, S. S; PERRY, T. L; DAKSHINAMURTI, K et al.Epilepsia (Copenhagen). 1984, Vol 25, Num 4, pp 457-463, issn 0013-9580Article

TYROSINOSE CONGENITALE (A PROPOS DE DEUX OBSERVATIONS)JOUANNOT LE BRIS FRANCOISE.1980; ; FRA; DA. 1980; 93; 62-VIII P.: ILL.; 30 CM; BIBL. 49 REF.; TH.: MED./ROUEN/1980Thesis

TYROSINEMIE HEREDITAIRE. EXAMEN DU FOIE EN MICROSCOPIE ELECTRONIQUE DE BIOPSIES HEPATIQUES. OBSERVATION DE SEPT CAS.TREMBLAY M; BELANGER L; LAROCHELLE J et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 7; PP. 1014-1016; ABS. ANGL.; BIBL. 7 REF.Article

DIAGNOSE UND THERAPIE SECHS ERBBEDINGTER ZU SCHWACHSINN FUEHRENDER STOFFWECHSELSTOERUNGEN II = DIAGNOSTIC ET TRAITEMENT DE SIX MALADIES HEREDITAIRES METABOLIQUES ENTRAINANT UNE DEBILITE MENTALE IIMENNE F; ENZENAUER J; MATZ D et al.1976; MED. KLIN.; DTSCH.; DA. 1976; VOL. 71; NO 18; PP. 772-785; BIBL. 43 REF.Article

LE RESEAU DE MEDECINE GENETIQUE DU QUEBEC. UN PROGRAMME INTEGRE DU DIAGNOSTIC, CONSEIL ET TRAITEMENT DES MALADIES METABOLIQUES HEREDITAIRESLABERGE C; SCRIVER CR; CLOW CL et al.1975; UN. MED. CANADA; CANADA; DA. 1975; VOL. 104; NO 3; PP. 428-432; ABS. ANGL.; BIBL. 25REF.Article

ETUDE IN VITRO DE L'ADENYLCYCLASE HEPATIQUE DANS DES CAS DE TYROSINEMIE HEREDITAIRELESCAULT A; LABERGE C.1974; UN. MED. CANADA; CANADA; DA. 1974; VOL. 103; NO 12; PP. 2137-2139; ABS. ANGL.; BIBL. 5REF.Article

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