William B. Rizzo
Department of Pediatrics
University of Nebraska Medical Center
985456 Nebraska Medical Center
Omaha
USA
Name/email consistency: high
- Ichthyosis in Sjögren-Larsson syndrome reflects defective barrier function due to abnormal lamellar body structure and secretion. Rizzo, W.B., S'Aulis, D., Jennings, M.A., Crumrine, D.A., Williams, M.L., Elias, P.M. Arch. Dermatol. Res. (2010)
- Abnormal fatty alcohol metabolism in cultured keratinocytes from patients with Sjögren-Larsson syndrome. Rizzo, W.B., Craft, D.A., Somer, T., Carney, G., Trafrova, J., Simon, M. J. Lipid Res. (2008)
- Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency. Rizzo, W.B. Mol. Genet. Metab. (2007)
- Sjögren-Larsson syndrome: diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2). Rizzo, W.B., Carney, G. Hum. Mutat. (2005)