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Simple Search
Hits 1 – 7 of 7
1
The TMEM106B risk allele is associated with lower cortical volumes in a clinically diagnosed frontotemporal dementia cohort.
Harding, SR
;
Bocchetta, M
;
Gordon, E
...
In: J Neurol Neurosurg Psychiatry (2017) (2017)
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2
Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.
Rohrer, JD
;
Beck, J
;
Plagnol, V
...
In: J Neurol Neurosurg Psychiatry , 84 (12) pp. 1411-1412. (2013) (2013)
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3
Progressive logopenic/phonological aphasia: Erosion of the language network
Rohrer, JD
;
Ridgway, GR
;
Crutch, SJ
...
In: NEUROIMAGE , 49 (1) 984 - 993. (2010) (2010)
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4
The heritability and genetics of frontotemporal lobar degeneration
Rohrer, JD
;
Guerreiro, R
;
Vandrovcova, J
...
In: NEUROLOGY , 73 (18) 1451 - 1456. (2009) (2009)
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5
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series
Beck, J
;
Rohrer, JD
;
Campbell, T
...
In: BRAIN , 131 706 - 720. (2008) (2008)
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6
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene
Rohrer, JD
;
Warren, JD
;
Omar, R
...
In: ARCH NEUROL-CHICAGO , 65 (4) 506 - 513. (2008) (2008)
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7
Mapping the progression of progranulin-associated frontotemporal lobar degeneration
Rohrer, JD
;
Warren, JD
;
Barnes, J
...
In: NAT CLIN PRACT NEURO , 4 (8) 455 - 460. (2008) (2008)
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