Neuropathologic heterogeneity in HDDD1 : A familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and Progranulin mutationBEHRENS, Maria I; MUKHERJEE, Odity; CHAKRAVERTY, Sumi et al.Alzheimer disease and associated disorders. 2007, Vol 21, Num 1, pp 1-7, issn 0893-0341, 7 p.Article

Association of TMEM106B Gene Polymorphism With Age at Onset in Granulin Mutation Carriers and Plasma Granulin Protein LevelsCRUCHAGA, Carlos; GRAFF, Caroline; GOATE, Alison et al.Archives of neurology (Chicago). 2011, Vol 68, Num 5, pp 581-586, issn 0003-9942, 6 p.Article

TDP-43 A315T Mutation in Familial Motor Neuron DiseaseGITCHO, Michael A; BALOH, Robert H; BAKER, Matt et al.Annals of neurology. 2008, Vol 63, Num 4, pp 535-538, issn 0364-5134, 4 p.Article