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Animal models reveal pathophysiologies of tyrosinemiasENDO, Fumio; TANAKA, Yasuhiko; TOMOEDA, Kaede et al.The Journal of nutrition. 2003, Vol 133, Num 6, pp 2063-2067, issn 0022-3166, 5 p., SUP1Conference Paper

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

HEREDITARY TYROSINEMIA AND THE HEME BIOSYNTHETIC PATHWAY: PROFOUND INHIBITION OF DELTA -AMINOLEVULINIC ACID DEHYDRATASE ACTIVITY BY SUCRINYLACETONESASSA S; KAPPAS A.1983; JOURNAL OF CLINICAL INVESTIGATION; ISSN 0021-9738; USA; DA. 1983; VOL. 71; NO 3; PP. 625-634; BIBL. 41 REF.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

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

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

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

PRESENTAZIONE DI UN CASO DI TIROSINEMIA TIPO 1, FORMA CRONICA. TRATTAMENTO DIETETICO E DECORSO CLINICO = PRESENTATION D'UN CAS DE TYROSINEMIE DE TYPE 1, FORME CHRONIQUE. TRAITEMENT DIETETIQUE ET EVOLUTION CLINIQUEGABRIELLI O; MAIORANA A; PARIS D et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 16; PP. 1329-1334; ABS. ENG; BIBL. 20 REF.Article

UNUSUAL PATTERN OF METABOLITES IN THE URINE OF A CHILD WITH TYROSINEMIA: GLYCERALDEHYDE.TOMER KB; ROTHMAN R; YUDKOF M et al.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 81; NO 2; PP. 109-117; BIBL. 13 REF.Article

HEPATIC TYROSINE AMINOTRANSFERASE IN TYROSINAEMIA TYPE IIKIDA K; TAKAHASHI M; FUJISAWA Y et al.1982; JOURNAL OF INHERITED METABOLIC DISEASE; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; NO 4; PP. 229-230; BIBL. 7 REF.Article

STUDIO DELLO SVILUPPO NEUROPSICHICO IN UN GRUPPO DI BAMBINI CON TIROSINEMIA TRANSITORIA NEONATALE. = ETUDE DU DEVELOPPEMENT NEUROPSYCHIQUE D'UN GROUPE D'ENFANTS ATTEINTS DE TYROSINEMIE TRANSITOIRE NEONATALEDI CAGNO L; RIGARDETTO R; BIANCO M et al.1978; NEUROPSICHIATR. INFANT.; ITA; DA. 1978; NO 200; PP. 227-247; ABS. ENG; BIBL. 26 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

Neurologic crises in hereditary tyrosinemiaMITCHELL, G; LAROCHELLE, J; KHAZAL PARADIS et al.The New England journal of medicine. 1990, Vol 322, Num 7, pp 432-437, issn 0028-4793Article

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

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

Tyrosinemia type I : Diagnostic issues and prenatal diagnosisBIJARNIA, Sunita; PURI, Ratna D; RUEL, Jean et al.Indian journal of pediatrics. 2006, Vol 73, Num 2, pp 163-165, issn 0019-5456, 3 p.Article

Determination of urinary succinylacetone by capillary gas chromatographyTUCHMAN, M; WHITLEY, C. B; RAMNARAINE, M. L et al.Journal of chromatographic science. 1984, Vol 22, Num 5, pp 211-215, issn 0021-9665Article

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