au.\*:("BATSHAW, Mark L")
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Brain development and the ontogeny of developmental disabilitiesACOSTA, Maria; GALLO, Vittorio; BATSHAW, Mark L et al.Advances in pediatrics. 2002, Vol 49, pp 1-57, issn 0065-3101, 57 p.Article
Humoral immune response to recombinant adenovirus and adeno-associated virus after in utero administration of viral vectors in miceJEREBTSOVA, Marina; BATSHAW, Mark L; XUEHAI YE et al.Pediatric research. 2002, Vol 52, Num 1, pp 95-104, 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
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
Prospects for prenatal gene therapy in disorders causing mental retardationXUEHAI YE; MITCHELL, Melanie; NEWMAN, Kurt et al.Mental retardation and developmental disabilities research reviews. 2001, Vol 7, Num 1, pp 65-72, issn 1080-4013Article
Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiencyGYATO, Kunsang; WRAY, J; HUANG, Z. J et al.Annals of neurology. 2004, Vol 55, Num 1, pp 80-86, issn 0364-5134, 7 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
Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectorsXUEHAI YE; ZIMMER, Klaus-Peter; BROWN, Rebecca et al.Human gene therapy. 2001, Vol 12, Num 9, pp 1035-1046, issn 1043-0342Article
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
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
A pilot study of in vivo liver-directed gene transfer with an adenoviral vector in partial ornithine transcarbamylase deficiencyRAPER, Steven E; YUDKOFF, Marc; SIMOES, Heather et al.Human gene therapy. 2002, Vol 13, Num 1, pp 163-175, issn 1043-0342Article
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