William L. Nyhan
Department of Pediatrics
University of California
San Diego
California
USA
Name/email consistency: high
- Positive newborn screen in the biochemically normal infant of a mother with treated holocarboxylase synthetase deficiency. Nyhan, W.L., Willis, M., Barshop, B.A., Gangoiti, J. J. Inherit. Metab. Dis. (2009)
- Lesch-Nyhan disease. Nyhan, W.L. Nucleosides. Nucleotides. Nucleic. Acids (2008)
- Inherited hyperuricemic disorders. Nyhan, W.L. Contrib. Nephrol (2005)
- Lesch-Nyhan Disease. Nyhan, W.L. J. Hist. Neurosci (2005)
- Disorders of purine and pyrimidine metabolism. Nyhan, W.L. Mol. Genet. Metab. (2005)
- Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liver. Nyhan, W.L., Gargus, J.J., Boyle, K., Selby, R., Koch, R. Eur. J. Pediatr. (2002)
- Dopamine function in Lesch-Nyhan disease. Nyhan, W.L. Environ. Health Perspect. (2000)