William Leo Nyhan - bibliography
American paediatrician, born March 13, 1926.
- William L. Nyhan, editor:
Heritable disorders of amino acid metabolism: patterns of clinical expression and genetic variation. New York, John Wiley & Sons, 1974.
- William Leo Nyhan, editor:
Abnormalities in Amino Acid Metabolism in Clinical Medicine.
Norwalk : Appleton-Century-Crofts, 1984.
- William L. Nyhan, Nadia A. Sakati:
Diagnostic Recognition of Genetic Disease. Philadelphia: Lea and Febiger, 1987.
- R. L. Hamilton, R. H. Haas, W. L. Nyhan, H. C. Powell, M. R. Grafe:
Neuropathology of propionic acidemia: a report of two patients with basal ganglia lesions.
Journal of Child Neurology, January 1995, 10 (1): 25-30.
- W. L. Nyhan, J. J. Gargus, K. Boyle, R. Selby, R. Koch:
Progressive neurologic disability in methylmalonic acidemia despite transplantation of the liver. European Journal of Pediatrics, July 2002, 161 (7): 377-379.
- W. L. Nyhan:
Disorders of purine and pyrimidine metabolism.
Molecular Genetics and Metabolism, Orlando. Florida, 2005, 86: 25-33.
I this article the connections between levels of uric acid in blood of patients with Lesch-Nyhan syndrome are linked to clinical symptoms. Biographical:
- Peter Beighton & Gretha Beighton:
The Man Behind the Syndrome.
Springer Verlag, Berlin-Heidelberg-New York-Tokyo, 1986: 221.