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ti.\*:("Satellite Symposium on Advances in Inherited Urea Cycle Disorders")

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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

Evaluation of gene therapy for citrullinaemia using murine and bovine modelsPATEJUNAS, G; LEE, B; O'BRIEN, W. E et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 138-150, issn 0141-8955, SUP1Conference Paper

The biochemical and molecular spectrum of ornithine transcarbamylase deficiencyTUCHMAN, M; MORIZONO, H; RAJAGOPAL, B. S et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 40-58, issn 0141-8955, SUP1Conference Paper

Effects of hyperammonaemia on brain functionBUTTERWORTH, R. F.Journal of inherited metabolic disease. 1998, Vol 21, pp 6-20, issn 0141-8955, SUP1Conference Paper

Intragenic complementation at the argininosuccinate lyase locus : Reconstruction of the active siteHOWELL, P. L; TURNER, M. A; CHRISTODOULOU, J et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 72-85, issn 0141-8955, SUP1Conference Paper

Neurodevelopmental outcome of long-term therapy of urea cycle disorders in JapanUCHINO, T; ENDO, F; MATSUDA, I et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 151-159, issn 0141-8955, SUP1Conference Paper

The human arginases and arginase deficiencyIYER, R; JENKINSON, C. P; VOCKLEY, J. G et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 86-100, issn 0141-8955, SUP1Conference Paper

Alternative pathway therapy for urea cycle disordersFEILLET, F; LEONARD, J. V.Journal of inherited metabolic disease. 1998, Vol 21, pp 101-111, issn 0141-8955, SUP1Conference Paper

Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiencyRAPER, S. E; WILSON, J. M; YUDKOFF, M et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 119-137, issn 0141-8955, SUP1Conference Paper

In vivo measurement of ureagenesis with stable isotopesYUDKOFF, M; DAIKHIN, Y; YE, X et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 21-29, issn 0141-8955, SUP1Conference Paper

Liver transplantation for the treatment of urea cycle disordersWHITINGTON, P. F; ALONSO, E. M; BOYLE, J. T et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 112-118, issn 0141-8955, SUP1Conference Paper

Regulation of the urea cycle enzyme genes in nitric oxide synthesisMORI, M; GOTOH, T; NAGASAKI, A et al.Journal of inherited metabolic disease. 1998, Vol 21, pp 59-71, issn 0141-8955, SUP1Conference Paper

Molecular genetic research into carbamoyl-phosphate synthase I: Molecular defects and linkage markersSUMMAR, M. L.Journal of inherited metabolic disease. 1998, Vol 21, pp 30-39, issn 0141-8955, SUP1Conference Paper

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