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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

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

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

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

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

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

HEREDITARY TYROSINAEMIA. CLINICAL, ENZYMATIC, AND PATHOLOGICAL STUDY OF AN INFANT WITH THE ACUTE FORM OF THE DISEASECARSON NAJ; BIGGART JD; BITTLES AH et al.1976; ARCH. DIS. CHILDH.; G.B.; DA. 1976; VOL. 51; NO 2; PP. 106-113; BIBL. 30 REF.Article

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

CLINICAL SIGNIFICANCE OF TYROSINEMIA OF PREMATURITY = SIGNIFICATION CLINIQUE DE LA TYROSINEMIE DE LA PREMATURITELIGHT IJ; SUTHERLAND JM; BERRY HK et al.1973; AMER. J. DIS. CHILD.; U.S.A.; DA. 1973; VOL. 125; NO 2; PP. 243-247; BIBL. 24 REF.Serial Issue

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

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

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

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

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

Liver transplantation in tyrosinaemia type I : the Groningen experienceWIJBURG, F. A; REITSMA, W. C. C; SLOOFF, M. J. H et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 115-118, issn 0141-8955Article

Vier Fälle von Richner-Hanhart-Syndrom (Tyrosinämie Typ II) mit neurologischer Symptomatologie in einer jugoslawischen Familie = Quatre cas de syndrome de Richner-Hanhart (tyrosinémie de type II) avec symptomatologie neurologique dans une famille yougoslave = Four cases of Richner-Hanhart syndrome (tyrosinemia type II) with neurological synptome in a Yugoslavian familySALAMON, T; HRNJICA, M; SCHNYDER, U. W et al.Hautarzt. 1988, Vol 39, Num 3, pp 149-154, issn 0017-8470Article

Tyrosinaemia type I : considerations of treatment strategy and experiences with risk assessment, diet and transplantationVAN SPRONSEN, F. J; SMIT, G. P. A; WIJBURG, F. A et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 111-114, issn 0141-8955Article

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

TYROSINEMIA AND TYROSYLURIA IN HEALTHY PREMATURES: TIME COURSES NOT VITAMIN C-DEPENDENT = LA TYROSINEMIE ET LA TYROSYLURIE CHEZ LES PREMATURES NORMAUX. EVOLUTION DANS LE TEMPS INDEPENDANTE DE LA VITAMINE CBAKKER HD; WADMAN SK; VAN SPRANG FJ et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 61; NO 1; PP. 73-90; BIBL. 43REF.Article

ULTRAVIOLET FLUORESCENCE SPECTRA OF THE CEREBROSPINAL FLUID IN TYROSINAEMIA = LE SPECTRE DE FLUORESCENCE A L'ULTRA-VIOLET DU LIQUIDE CEREBRO-SPINAL DANS LA TYROSINEMIEHEYNE K.1972; ACTA PAEDIATR. ACAD. SCI. HUNGAR.; HONGR.; DA. 1972; VOL. 13; NO 1; PP. 89-94; ABS. RUSSE; BIBL. 16 REF.Serial Issue

Liver transplantation in nine Spanish patients wity tyrosinaemia type IPEREZ-CERDA, C; MERINERO, B; SANZ, P et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 2, pp 119-122, issn 0141-8955Article

BIOCHEMICAL STUDIES IN A PATIENT WITH TYROSINOSIS = ETUDE BIOCHIMIQUE CHEZ UN MALADE ATTEINT DE TYROSINOSELOUIS WJ; PITT DD; DAVIES H et al.1974; AUSTRAL. NEW ZEAL. J. MED.; AUSTRAL.; DA. 1974; VOL. 4; NO 3; PP. 281-286; BIBL. 13REF.Article

Imaging features of type 1 hereditary tyrosinemia : a review of 30 patientsDUBOIS, J; GAREL, L; PATRIQUIN, H et al.Pediatric radiology. 1996, Vol 26, Num 12, pp 845-851, issn 0301-0449Article

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