Biblio
Found 4 results
Filters: Author is Graff-Radford,Neill R. [Clear All Filters]
[2728]
(2012). Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families.
PLoS ONE. 7(2), e31039 - e31039.
[2257]
(2011). Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Nat Genet. 43(5), 436 - 441.
[1893]
(2010). Occupation attributes relate to location of atrophy in frontotemporal lobar degeneration.
Neuropsychologia. 48(12), 3634 - 3641.
[1164]
(2007). Progranulin Mutations in Primary Progressive Aphasia: The PPA1 and PPA3 Families.
Arch Neurol. 64(1), 43 - 47.
