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PLOS GENETICS (2017)
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Serggio C. Lanata et al.
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Marisa Kamelgarn et al.
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Vaclav Janousek et al.
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Atsushi Yamaguchi et al.
SCIENTIFIC REPORTS (2016)
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M. Carolina Gallego-Iradi et al.
PLOS ONE (2015)
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PSYCHIATRIC CLINICS OF NORTH AMERICA (2015)
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Janel O. Johnson et al.
NATURE NEUROSCIENCE (2014)
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Shuo-Chien Ling et al.
NEURON (2013)
The epidemiology of frontotemporal dementia
Chiadi U. Onyike et al.
INTERNATIONAL REVIEW OF PSYCHIATRY (2013)
Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia
Katya Rascovsky et al.
BRAIN (2011)
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Harro Seelaar et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
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Jennifer Merrilees et al.
AMYOTROPHIC LATERAL SCLEROSIS (2010)
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Ian R. A. Mackenzie et al.
LANCET NEUROLOGY (2010)
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Jan Senderek et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
The molecular basis of frontotemporal dementia
Manuela Neumann et al.
EXPERT REVIEWS IN MOLECULAR MEDICINE (2009)
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JS Goldman et al.
NEUROLOGIST (2004)