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Results 1 to 25 of 508

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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

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

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

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

Intellectual, Adaptive, and Behavioral Functioning in Children With Urea Cycle DisordersKRIVITZKY, Lauren; BABIKIAN, Talin; LEE, Hye-Seung et al.Pediatric research. 2009, Vol 66, Num 1, pp 96-101, issn 0031-3998, 6 p.Article

Arginine challenge unravels persistent disturbances of urea cycle and gluconeogenesis in abstinent alcoholicsHASSELBLATT, Martin; KRAMPE, Henning; JACOBS, Silke et al.Alcohol and alcoholism (Oxford). 2006, Vol 41, Num 4, pp 372-378, issn 0735-0414, 7 p.Article

Urea cycle intermediate kinetics and nitrate excretion at normal and therapeutic intakes of arginine in humansBEAUMIER, L; CASTILLO, L; AJAMI, A. M et al.American journal of physiology. Endocrinology and metabolism. 1995, Vol 32, Num 5, pp E884-E896, issn 0193-1849Article

Coordinate induction of the urea cycle enzymes by glucagon and dexamethasone is accomplished by three different mechanismsULBRIGHT, C; SNODGRASS, P. J.Archives of biochemistry and biophysics (Print). 1993, Vol 301, Num 2, pp 237-243, issn 0003-9861Article

Effect of ammonium chloride on homocitrulline and homoarginine synthesis from lysineKATO, T; SANO, M.Journal of inherited metabolic disease. 1993, Vol 16, Num 5, pp 906-907, issn 0141-8955Article

Hyperammoniémie et déficit héréditaires du cycle de l'uréeRABIER, D; CATHELINEAU, L.Le Pédiatre. 1990, Vol 26, Num 124, pp 205-215, issn 0397-9180, 10 p.Article

Mammalian urea cycle enzymesJACKSON, M. J; BEAUDET, A. L; O'BRIEN, W. E et al.Annual review of genetics. 1986, Vol 20, pp 431-464, issn 0066-4197Article

Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiencyBATSHAW, M. L; MSALL, M; BEAUDET, A. L et al.The Journal of pediatrics. 1986, Vol 108, Num 2, pp 236-241, issn 0022-3476Article

Early Clinical Manifestations and Eating Patterns in Patients with Urea Cycle DisordersGARDEITCHIK, Thatjana; HUMPHREY, Maureen; NATION, Judy et al.The Journal of pediatrics. 2012, Vol 161, Num 2, pp 328-332, issn 0022-3476, 5 p.Article

Long-term outcome and intervention of urea cycle disorders in JapanKIDO, Jun; NAKAMURA, Kimitoshi; HORIKAWA, Reiko et al.Journal of inherited metabolic disease. 2012, Vol 35, Num 5, pp 777-785, issn 0141-8955, 9 p.Article

Evolution and metabolic significance of the urea cycle in photosynthetic diatomsALLEN, Andrew E; DUPONT, Christopher L; BOWLER, Chris et al.Nature (London). 2011, Vol 473, Num 7346, pp 203-207, issn 0028-0836, 5 p.Article

Hereditary urea cycle diseases in FinlandKESKINEN, Päivi; SIITONEN, Anna; SALO, Matti et al.Acta paediatrica (Oslo). 2008, Vol 97, Num 10, pp 1412-1419, issn 0803-5253, 8 p.Article

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