Pascal and Francis Bibliographic Databases

Help

Search results

Your search

au.\*:("TUCHMAN, Mendel")

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 25

  • Page / 1
Export

Selection :

  • and

Proceedings of a consensus conference for the management of patients with Urea Cycle DisordersSUMMAR, Marshall; TUCHMAN, Mendel.The Journal of pediatrics. 2001, Vol 138, Num 1, pp S6-S10, issn 0022-3476, SUPConference Paper

Expression of wild-type and mutant human ornithine transcarbamylase genes in chinese hamster ovary cells and lack of dominant negative effect of R141Q and R40H mutantsAUGUSTIN, Lance; MAVINAKERE, Manohara; MORIZONO, Hiroki et al.Pediatric research. 2000, Vol 48, Num 6, pp 842-846, issn 0031-3998Article

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

Alternative pathway therapy for urea cycle disorders : Twenty years laterBATSHAW, Mark L; MACARTHUR, Robert B; TUCHMAN, Mendel et al.The Journal of pediatrics. 2001, Vol 138, Num 1, pp S46-S55, issn 0022-3476, SUPConference Paper

Quantification of benzoic, phenylacetic, and phenylbutyric acids from filter-paper blood spots by gas chromatography-mass spectrometry with stable isotope dilutionXIAOLIN YU; THOMPSON, Mark M; DASHUANG SHI et al.Clinical chemistry (Baltimore, Md.). 2001, Vol 47, Num 2, pp 351-354, issn 0009-9147Conference 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

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

Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemiaCALDOVIC, Ljubica; MORIZONO, Hiroki; PANGLAO, Maria Gracia et al.Human genetics. 2003, Vol 112, Num 4, pp 364-368, issn 0340-6717, 5 p.Article

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

Health and economic benefits of well-designed evaluations : Some lessons from evaluating neuroblastoma screeningSODERSTROM, Lee; WOODS, William G; BERNSTEIN, Mark et al.Journal of the National Cancer Institute. 2005, Vol 97, Num 15, pp 1118-1124, issn 0027-8874, 7 p.Article

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

Screening of infants and mortality due to neuroblastomaWOODS, William G; GAO, Ru-Nie; TUCHMAN, Mendel et al.The New England journal of medicine. 2002, Vol 346, Num 14, pp 1041-1046, issn 0028-4793Article

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

N-carbamylglutamate Markedly Enhances Ureagenesis in N-acetylglutamate Deficiency and Propionic Acidemia as Measured by Isotopic Incorporation and Blood BiomarkersTUCHMAN, Mendel; CALDOVIC, Ljubica; DAIKHIN, Yevgeny et al.Pediatric research. 2008, Vol 64, Num 2, pp 213-217, issn 0031-3998, 5 p.Article

Restoration of ureagenesis in N-acetylglutamate synthase deficiency by N-carbamylglutamateCALDOVIC, Ljubica; MORIZONO, Hiroki; DAIKHIN, Yevgeny et al.The Journal of pediatrics. 2004, Vol 145, Num 4, pp 552-554, issn 0022-3476, 3 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

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

Significant behavioral disturbances in succinic semialdehyde dehydrogenase (SSADH) deficiency (gamma-hydroxybutyric aciduria)GIBSON, K. Michael; GUPTA, Maneesh; PEARL, Phillip L et al.Biological psychiatry (1969). 2003, Vol 54, Num 7, pp 763-768, issn 0006-3223, 6 p.Article

Brain MR imaging in neonatal hyperammonemic encephalopathy resulting from proximal urea cycle disordersTAKANASHI, Jun-Ichi; BARKOVICH, A. James; CHENG, Sabrina F et al.American journal of neuroradiology. 2003, Vol 24, Num 6, pp 1184-1187, issn 0195-6108, 4 p.Article

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

Acetylornithine transcarbamylase : a novel enzyme in arginine biosynthesisMORIZONO, Hiroki; CABRERA-LUQUE, Juan; DASHUANG SHI et al.Journal of bacteriology. 2006, Vol 188, Num 8, pp 2974-2982, issn 0021-9193, 9 p.Article

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

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

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

  • Page / 1