| 2006 | HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin | Mukherjee, O.; Pastor, P.; Cairns, N. J.; Chakraverty, S.; Kauwe, J. S.; Shears, S.; Behrens, M. I.; Budde, J.; Hinrichs, A. L.; Norton, J.; Levitch, D.; Taylor-Reinwald, L.; Gitcho, M.; Tu, P. H.; Tenenholz Grinberg, L.; Liscic, R. M.; Armendariz, J.; Morris, J. C.; Goate, A. M. | Ann Neurol 60(3), 314-322 | | | |
| 2007 | Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation | Behrens, M. I.; Mukherjee, O.; Tu, P. H.; Liscic, R. M.; Grinberg, L. T.; Carter, D.; Paulsmeyer, K.; Taylor-Reinwald, L.; Gitcho, M.; Norton, J. B.; Chakraverty, S.; Goate, A. M.; Morris, J. C.; Cairns, N. J. | Alz Dis Assoc Dis 21(1), 1-7 | | | |
