Skip navigation
Skip to main content

Search


Current filters:
Start a new search
Add filters:

Use filters to refine the search results.


Results 1-10 of 24 (Search time: 0.001 seconds).
Item hits:
PreviewIssue DateTitleAuthor(s)
2017Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathiesForrest, SL; Kril, JJ; Stevens, C; Kwok, JB; Hallupp, M; Kim, W; Huang, Y; McGinley, C; Werka, H; Kiernan, MC; Gotz, J; Spillantini, MG; Hodges, JR; Ittner, LM; Halliday, GM
18-Oct-2016[18F]AV-1451 PET in behavioural variant frontotemporal dementia due to MAPT mutationBevan Jones, WR; Cope, TE; Passamonti, L; Fryer, TD; Hong, YT; Aigbirhio, F; Kril, JJ; Forrest, SL; Allinson, K; Coles, JP; Spillantini, MG; Hodges, JR; O'Brien, JT; Rowe, JB
29-May-2017Assessment of amyloid β in pathologically confirmed frontotemporal dementia syndromesTan, RH; Kril, JJ; Yang, Y; Tom, N; Hodges, JR; Villemagne, VL; Rowe, CC; Leyton, CE; Kwok, JBJ; Ittner, LM; Halliday, GM
8-Apr-2016Expanding the phenotypic associations of globular glial tau subtypesBurrell, JR; Forrest, SL; Bak, TH; Hodges, JR; Halliday, GM; Kril, JJ
2005A mutation in bovine keratin 5 causing epidermolysis bullosa simplex, transmitted by a mosaic sireFord, CA; Stanfield, AM; Spelman, RJ; Smits, B; Ankersmidt-Udy, AE; Cottier, K; Holloway, H; Walden, A; Al-Wahb, M; Bohm, E; Snell, RG; Sutherland, G
2003Molecular investigation of TBP allele length: a SCA17 cellular model and population studyReid, SJ; Rees, MI; van Room-Mom, WM; Jones, AL; MacDonald, ME; Sutherland, G; During, MJ; Faull, RL; Owen, MJ; Dragunow, M; Snell, RG
2010Disease-specific, neurosphere-derived cells as models for brain disordersMatigian, N; Abrahamsen, G; Sutharsan, R; Cook, AL; Vitale, AM; Nouwens, A; Bellette, B; An, J; Anderson, M; Beckhouse, AG; Bennebroek, M; Cecil, R; Chalk, AM; Cochrane, J; Fan, Y; Féron, F; McCurdy, R; McGrath, JJ; Murrell, W; Perry, C; Raju, J; Ravishankar, S; Silburn, PA; Sutherland, GT; Mahler, S; Mellick, GD; Wood, SA; Sue, CM; Wells, CA; Mackay-Sim, A
2009A cross-study transcriptional analysis of Parkinson's diseaseSutherland, GT; Matigian, NA; Chalk, AM; Anderson, MJ; Silburn, PA; Mackay-Sim, A; Wells, CA; Mellick, GD
2009Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?Sutherland, GT; Halliday, GM; Silburn, PA; Mastaglia, FL; Rowe, DB; Boyle, RS; O'Sullivan, JD; Ly, T; Wilton, SD; Mellick, GD
2009Haplotype analysis of the PARK 11 gene, GIGYF2, in sporadic Parkinson's diseaseSutherland, GT; Siebert, GA; Newman, JR; Silburn, PA; Boyle, RS; O'Sullivan, JD; Mellick, GD