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au.\*:("BACHMANN, Claude")

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Outcome and survival of 88 patients with urea cycle disorders: a retrospective evaluationBACHMANN, Claude.European journal of pediatrics. 2003, Vol 162, Num 6, pp 410-416, issn 0340-6199, 7 p.Article

Long-term outcome of patients with urea cycle disorders and the question of neonatal screeningBACHMANN, Claude.European journal of pediatrics. Supplement. 2003, Vol 162, Num 1, pp S29-S33, issn 0943-9676Article

Interpretation of plasma amino acids in the follow-up of patients : The impact of compartmentationBACHMANN, Claude.Journal of inherited metabolic disease. 2008, Vol 31, Num 1, pp 7-20, issn 0141-8955, 14 p.Article

Mechanisms of hyperammonemiaBACHMANN, Claude.Clinical chemistry and laboratory medicine. 2002, Vol 40, Num 7, pp 653-662, issn 1434-6621, 10 p.Article

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

Differential expression of the cationic amino acid transporter 2(B) in the adult rat brain1BRAISSANT, Olivier; GOTOH, Tomomi; LOUP, Marc et al.Molecular brain research. 2001, Vol 91, Num 1-2, pp 189-195, issn 0169-328XArticle

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

Organic acids in the second morning urine in a healthy Swiss paediatric populationBOULAT, Olivier; GRADWOHL, Marianne; MATOS, Vera et al.Clinical chemistry and laboratory medicine. 2003, Vol 41, Num 12, pp 1642-1658, issn 1434-6621, 17 p.Article

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

N-Acetylglutamate synthase deficiency and the treatment of hyperammonemic encephalopathyELPELEG, Orly; SHAAG, Avraham; BEN-SHALOM, Efrat et al.Annals of neurology. 2002, Vol 52, Num 6, pp 845-849, issn 0364-5134, 5 p.Article

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

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

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

Serum paracetamol concentration: An alternative to X-rays to determine feeding tube location in the critically illBERGER, Mette M; WERNER, Dominique; REVELLY, Jean-Pierre et al.JPEN. Journal of parenteral and enteral nutrition. 2003, Vol 27, Num 2, pp 151-155, issn 0148-6071, 5 p.Article

Alteration of amino acid metabolism in neuronal aggregate cultures exposed to hypoglycaemic conditionsHONEGGER, Paul; BRAISSANT, Olivier; HENRY, Hugues et al.Journal of neurochemistry. 2002, Vol 81, Num 6, pp 1141-1151, issn 0022-3042Article

Endogenous synthesis and transport of creatine in the rat brain : an in situ hybridization studyBRAISSANT, Olivier; HENRY, Hugues; LOUP, Marc et al.Molecular brain research. 2001, Vol 86, Num 1-2, pp 193-201, issn 0169-328XArticle

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

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