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Results 1 to 25 of 705

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A radiochemical assay for argininosuccinate synthetase with [U-14C]AspartateRATNER, S.Analytical biochemistry. 1983, Vol 135, Num 2, pp 479-488, issn 0003-2697Article

The energy cost of urea synthesisUSHA ANAND; ANAND, C. V.Biochemical education. 1993, Vol 21, Num 4, pp 198-199, issn 0307-4412Article

Hyperlysinémie et hyperammoniémie = Hyperlysinemia and hyperammonemiaRABIER, D; PARVY, P; BERDET, J et al.Annales de biologie clinique (Paris). 1991, Vol 49, Num 1, pp 45-48, issn 0003-3898Conference Paper

Detection of urea cycle enzymopathies in childhoodTRAUNER, D. A; SELF, T. W.Archives of neurology (Chicago). 1984, Vol 41, Num 7, pp 758-760, issn 0003-9942Article

Evaluation of endogenous nitric oxide synthesis in congenital urea cycle enzyme defectsNAGASAKA, Hironori; TSUKAHARA, Hirokazu; TAKAYANAGI, Masaki et al.Metabolism, clinical and experimental. 2009, Vol 58, Num 3, pp 278-282, issn 0026-0495, 5 p.Article

Molecular basis of argininemia : identification of two discrete frame-shift deletions in the liver-type arginase geneHARAGUCHI, Y; APARICIO R., J. M; TAKIGUCHI, M et al.The Journal of clinical investigation. 1990, Vol 86, Num 1, pp 347-350, issn 0021-9738Article

Glutamine: precursor or nitrogen donor for citrulline synthesis?MARINI, Juan C; DIDELIJA, Inka Cajo; CASTILLO, Leticia et al.American journal of physiology. Endocrinology and metabolism. 2010, Vol 62, Num 1, issn 0193-1849, E69-E79Article

Survival after treatment with phenylacetate and benzoate for urea-cycle disordersENNS, Gregory M; BERRY, Susan A; BERRY, Gerard T et al.The New England journal of medicine. 2007, Vol 356, Num 22, pp 2282-2292, issn 0028-4793, 11 p.Article

Usefulness of magnetic resonance spectroscopy in urea cycle disordersROZE, Emmanuel; AZUAR, Carole; MENUEL, Carole et al.Pediatric neurology. 2007, Vol 37, Num 3, pp 222-225, issn 0887-8994, 4 p.Article

Fatal Initial Adult-Onset Presentation of Urea Cycle DefectLIEN, Jamie; NYHAN, William L; BARSHOP, Bruce A et al.Archives of neurology (Chicago). 2007, Vol 64, Num 12, pp 1777-1779, issn 0003-9942, 3 p.Article

Urea cycle activity and arginine formation in rainbow trout (Salmo gairdneri)CHIU, Y. N; AUSTIC, R. E; RUMSEY, G. L et al.The Journal of nutrition. 1986, Vol 116, Num 9, pp 1640-1650, issn 0022-3166Article

Citrullinemia presenting as uncontrollable epilepsyORIGUCHI, Y; USHIJIMA, T; SAKAGUCHI, M et al.Brain & development (Tokyo. 1979). 1984, Vol 6, Num 3, pp 328-331, issn 0387-7604Article

Interallic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiencyMCINNES, R. R; SHIH, V; CHILTON, S et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1984, Vol 81, Num 14, pp 4480-4484, issn 0273-1134Article

A new french-canadian family affected by hyperargininaemiaQURESHI, I. A; LETARTE, J; OUELLET, R et al.Journal of inherited metabolic disease. 1983, Vol 6, Num 4, pp 179-182, issn 0141-8955Article

Hyperammonemia in zinc deficiency: activities of urea cycle related enzymesCOSSACK, Z. T; PRASAD, A. S.Nutrition research (New York, NY). 1987, Vol 7, Num 11, pp 1161-1167, issn 0271-5317Article

Pyruvate-carboxylase deficiency with urea cycle impairmentGRETER, J; GUSTAFSSON, J; HOLME, E et al.Acta paediatrica scandinavica. 1985, Vol 74, Num 6, pp 982-986, issn 0001-656XArticle

Clinical features of carbamyl phosphate synthetase-I deficiency in an adultCALL, G; SEAY, A. R; SHERRY, R et al.Annals of neurology. 1984, Vol 16, Num 1, pp 90-93, issn 0364-5134Article

Satellite Symposium on Advances in Inherited Urea Cycle DisordersBATSHAW, Mark L; BACHMANN, Claude; TUCHMAN, Mendel et al.Journal of inherited metabolic disease. 1998, Vol 21, issn 0141-8955, 159 p., SUP1Conference Proceedings

Ammonium ion excretion and ureagenesis in acid-base balanceMCCORQUODALE, D. J.Biochemical education. 1992, Vol 20, Num 4, pp 219-222, issn 0307-4412Article

Neonatal citrullinaemia with satisfactory mental developmentSANJURJO, P; RODRIGUEZ-SORIANO, J; VALLO, A et al.European journal of pediatrics. 1991, Vol 150, Num 10, pp 730-731, issn 0340-6199Article

Evidence of inherited urea cycle defect in a case of fatal valproate toxicityHJELM, M; DE SILVA, L. V. K; SEAKINS, J. W. T et al.British medical journal (1857). 1986, Vol 292, Num 6512, pp 23-24, issn 0007-1447Article

The role of the urea cycle and polyamines in albumin synthesisORATZ, M; ROTHSCHILD, M. A; SCHREIBER, S. S et al.Hepatology (Baltimore, Md.). 1983, Vol 3, Num 4, pp 567-571, issn 0270-9139Article

Creatine metabolism in urea cycle defectsBOENZI, Sara; PASTORE, Anna; MARTINELLI, Diego et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 4, pp 647-653, issn 0141-8955, 7 p.Conference Paper

L'aspartate et son potentiel ergogène = Aspartate and its ergogenic potentialTRUDEAU, F.Science & sports. 1996, Vol 11, Num 4, pp 223-232, issn 0765-1597Article

A rapid method for determination of hepatic amino nitrogen to urea nitrogen conversion (the functional hepatic nitrogen clearance)HAMBERG, O; VILSTRUP, H.Scandinavian journal of clinical & laboratory investigation. 1994, Vol 54, Num 5, pp 377-383, issn 0036-5513Article

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