Phenotypic correction of ornithine transcarbamylase deficiency using low dose helper-dependent adenoviral vectors-Reference-Cited by-同舟云学术

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Phenotypic correction of ornithine transcarbamylase deficiency using low dose helper-dependent adenoviral vectors

Published:2008-08 Issue:8 Volume:10 Page:890-896
ISSN:1099-498X
Container-title:The Journal of Gene Medicine
language:en
Short-container-title:J. Gene Med.

Author:

Brunetti-Pierri Nicola,Clarke Christian,Mane Viraj,Palmer Donna J.,Lanpher Brendan,Sun Qin,O'Brien William,Lee Brendan

Publisher

Wiley

Subject

Genetics(clinical),Drug Discovery,Genetics,Molecular Biology,Molecular Medicine

Reference27 articles.

1. Neonatal onset ornithine transcarbamylase deficiency: a retrospective analysis;Maestri;J Pediatr,1999

2. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies;Msall;N Engl J Med,1984

3. Survival after treatment with phenylacetate and benzoate for urea-cycle disorders;Enns;N Engl J Med,2007

4. Liver transplantation for the treatment of urea cycle disorders;Whitington;J Inherit Metab Dis,1998

5. Developmental outcomes with early orthotopic liver transplantation for infants with neonatal-onset urea cycle defects and a female patient with late-onset ornithine transcarbamylase deficiency;McBride;Pediatrics,2004

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2. Predicting the disease severity in male individuals with ornithine transcarbamylase deficiency;Annals of Clinical and Translational Neurology;2022-10-10

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