Somatic GNAS Mutation Causes Widespread and Diffuse Pituitary Disease in Acromegalic Patients with McCune-Albright Syndrome

por Vortmeyer, Alexander O., Gläsker, Sven, Mehta, Gautam U., Abu-Asab, Mones S., Smith, Jonathan H., Zhuang, Zhengping, Collins, Michael T., Oldfield, Edward H.
Publicado 2012

Loss of Quiescence in von Hippel-Lindau Hemangioblastomas is Associated with Erythropoietin Signaling

por Feldman, Michael J., Sizdahkhani, Saman, Edwards, Nancy A., Merrill, Marsha J., Ray-Chaudhury, Abhik, Zhuang, Zhengping, Lonser, Russell R., Oldfield, Edward H., Chittiboina, Prashant
Publicado 2016

Safety and Feasibility of Long-term Intravenous Sodium Nitrite Infusion in Healthy Volunteers

por Pluta, Ryszard M., Oldfield, Edward H., Bakhtian, Kamran D., Fathi, Ali Reza, Smith, René K., DeVroom, Hetty L., Nahavandi, Masoud, Woo, Sukyung, Figg, William D., Lonser, Russell R.
Publicado 2011

Developmentally arrested structures preceding cerebellar tumors in von Hippel–Lindau disease

por Shively, Sharon B, Falke, Eric A, Li, Jie, Tran, Maxine G B, Thompson, Eli R, Maxwell, Patrick H, Roessler, Erich, Oldfield, Edward H, Lonser, Russell R, Vortmeyer, Alexander O
Publicado 2011

von Hippel-Lindau Disease-Associated Hemangioblastomas Are Derived from Embryologic Multipotent Cells

por Park, Deric M, Zhuang, Zhengping, Chen, Ling, Szerlip, Nicholas, Maric, Irina, Li, Jie, Sohn, Taesung, Kim, Stephanie H, Lubensky, Irina A, Vortmeyer, Alexander O, Rodgers, Griffin P, Oldfield, Edward H, Lonser, Russell R
Publicado 2007