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Neuroscience Letters|January 25, 2006
CHMP2B mutations are not a common cause of frontotemporal lobar degenerationAshley Cannon, Matthew Baker, Brad Boeve, et al.Brain Pathology (Zurich, Switzerland)|August 30, 2003
Hippocampal sclerosis dementia with tauopathyThomas G Beach, Lucia Sue, Sarah Scott, et al.Vision Research|November 13, 2004
Results from screening over 9000 mutation-bearing mice for defects in the electroretinogram and appearance of the fundusLawrence H Pinto, Martha Hotz Vitaterna, Sanda M Siepka, et al.BMJ Open|November 5, 2017
Long-Term Conditions Questionnaire (LTCQ): initial validation survey among primary care patients and social care recipients in EnglandCaroline M Potter, Laurie Batchelder, Christine A'Court, et al.Neurocase|April 27, 2021
Underlying pathology identified after 20 years of disease course in two cases of slowly progressive frontotemporal dementia syndromesFatma Ozlem Hokelekli, Jennifer L Whitwell, Mary M Machulda, et al.Brain : a Journal of Neurology|March 15, 2014
Regional distribution of synaptic markers and APP correlate with distinct clinicopathological features in sporadic and familial Alzheimer's diseaseMitsuru Shinohara, Shinsuke Fujioka, Melissa E Murray, et al.Journal of the International Neuropsychological Society : JINS|July 5, 2014
Early neuropsychological characteristics of progranulin mutation carriersBradley J Hallam, Claudia Jacova, Ging-Yuek R Hsiung, et al.Archives of Neurology|March 14, 2007
Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutationsJennifer L Whitwell, Clifford R Jack, Matthew Baker, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|September 30, 2006
Processes to activate phase III clinical trials in a Cooperative Oncology Group: the Case of Cancer and Leukemia Group BDavid M Dilts, Alan B Sandler, Matthew Baker, et al.Neurology|September 6, 2013
Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriersClaudia Jacova, Ging-Yuek R Hsiung, Itthipol Tawankanjanachot, et al.Pageof 13