Ruben Vidal
1Department of Pathology and Laboratory Medicine
Indiana University School of Medicine
635 Barnhill Dr. MSB A136
Indianapolis
USA
Name/email consistency: high
- The Psen1-L166P-knock-in mutation leads to amyloid deposition in human wild-type amyloid precursor protein YAC transgenic mice. Vidal, R., Sammeta, N., Garringer, H.J., Sambamurti, K., Miravalle, L., Lamb, B.T., Ghetti, B. FASEB J. (2012)
- Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy. Barbeito, A.G., Levade, T., Delisle, M.B., Ghetti, B., Vidal, R. Mol. Neurodegener (2010)
- Cerebral amyloid angiopathy and parenchymal amyloid deposition in transgenic mice expressing the Danish mutant form of human BRI2. Vidal, R., Barbeito, A.G., Miravalle, L., Ghetti, B. Brain Pathol. (2009)
- Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. Vidal, R., Miravalle, L., Gao, X., Barbeito, A.G., Baraibar, M.A., Hekmatyar, S.K., Widel, M., Bansal, N., Delisle, M.B., Ghetti, B. J. Neurosci. (2008)
- Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide gene. Vidal, R., Ghetti, B., Takao, M., Brefel-Courbon, C., Uro-Coste, E., Glazier, B.S., Siani, V., Benson, M.D., Calvas, P., Miravalle, L., Rascol, O., Delisle, M.B. J. Neuropathol. Exp. Neurol. (2004)
- Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. Vidal, R., Delisle, M.B., Ghetti, B. J. Neuropathol. Exp. Neurol. (2004)
- Hereditary ferritinopathy. Vidal, R., Delisle, M.B., Rascol, O., Ghetti, B. J. Neurol. Sci. (2003)
- Sequence, genomic structure and tissue expression of Human BRI3, a member of the BRI gene family. Vidal, R., Calero, M., Révész, T., Plant, G., Ghiso, J., Frangione, B. Gene (2001)