Ausgabe Sonderheft 1/1998
Inhalt (13 Artikel)
In vivo measurement of ureagenesis with stable isotopes
M. Yudkoff, Y. Daikhin, X. Ye, J. M. Wilson, M. L. Batshaw
The biochemical and molecular spectrum of ornithine transcarbamylase deficiency
M. Tuchman, H. Morizono, B. S. Rajagopal, R. J. Plante, N. M. Allewell
Regulation of the urea cycle enzyme genes in nitric oxide synthesis
M. Mori, T. Gotoh, A. Nagasaki, M. Takiguchi, T. Sonoki
Intragenic complementation at the argininosuccinate lyase locus: Reconstruction of the active site
P. L. Howell, M. A. Turner, J. Christodoulou, D. C. Walker, H. J. Craig, L. R. Simard, L. Ploder, R. R. McInnes
The human arginases and arginase deficiency
R. Iyer, C. P. Jenkinson, J. G. Vockley, R. M. Kern, W. W. Grody, S. Cederbaum
Liver transplantation for the treatment of urea cycle disorders
P. F. Whitington, E. M. Alonso, J. T. Boyle, J. P. Molleston, P. Rosenthal, J. C. Emond, J. M. Millis
Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency
S. E. Raper, J. M. Wilson, M. Yudkoff, M. B. Robinson, X. Ye, M. L. Batshaw
Evaluation of gene therapy for citrullinaemia using murine and bovine models
G. Patejunas, B. Lee, J. A. Dennis, P. J. Healy, P. J. Reeds, H. Yu, M. Frazer, B. Mull, A. W. Warman, A. L. Beaudet, W. E. O'Brien
Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan
T. Uchino, F. Endo, I. Matsuda