Neurology

Variation in Longevity Gene KLOTHO is Associated with Greater Cortical Volumes in Aging (S41.002).

Neurology

Jennifer Yokoyama, Virginia Sturm, Luke Bonham, Eric Klein, Konstantinos Arfanakis, Lei Yu, Giovanni Coppola, Joel Kramer, David Bennett, Bruce Miller, Dena Dubal

Practical utility of amyloid and FDG-PET in an academic dementia center.

Neurology

Sánchez-Juan P, Ghosh PM, Hagen J, Gesierich B, Henry M, Grinberg LT, O'Neil JP, Janabi M, Huang EJ, Trojanowski JQ, Vinters HV, Gorno-Tempini M, Seeley WW, Boxer AL, Rosen HJ, Kramer JH, Miller BL, Jagust WJ, Rabinovici GD

In vivo signatures of nonfluent/agrammatic primary progressive aphasia caused by FTLD pathology.

Neurology

Caso F, Mandelli ML, Henry M, Gesierich B, Bettcher BM, Ogar J, Filippi M, Comi G, Magnani G, Sidhu M, Trojanowski JQ, Huang EJ, Grinberg LT, Miller BL, Dronkers N, Seeley WW, Gorno-Tempini ML

Very low levels of education and cognitive reserve: a clinicopathologic study.

Neurology

Farfel JM, Nitrini R, Suemoto CK, Grinberg LT, Ferretti RE, Leite RE, Tampellini E, Lima L, Farias DS, Neves RC, Rodriguez RD, Menezes PR, Fregni F, Bennett DA, Pasqualucci CA, Jacob Filho W

B Cell Exchange across the Blood-Brain Barrier in Multiple Sclerosis (S11.003).

Neurology

H. Von Budingen, Tracy Kuo, Marina Sirota, Christopher van Belle, Leonard Apeltsin, Jacob Glanville, Bruce Cree, Pierre-Antoine Gourraud, Amy von Schwartzburg, Gabriella Huerta, Dilduz Telman, Purnima Sundar, Tyler Casey, David Cox, Stephen Hauser

Amyloid vs FDG-PET in the differential diagnosis of AD and FTLD.

Neurology

Rabinovici GD, Rosen HJ, Alkalay A, Kornak J, Furst AJ, Agarwal N, Mormino EC, O'Neil JP, Janabi M, Karydas A, Growdon ME, Jang JY, Huang EJ, Dearmond SJ, Trojanowski JQ, Grinberg LT, Gorno-Tempini ML, Seeley WW, Miller BL, Jagust WJ

Neuropathologic features associated with Alzheimer disease diagnosis: age matters.

Neurology

Middleton LE, Grinberg LT, Miller B, Kawas C, Yaffe K

Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations.

Neurology

Dibbens LM, Kneen R, Bayly MA, Heron SE, Arsov T, Damiano JA, Desai T, Gibbs J, McKenzie F, Mulley JC, Ronan A, Scheffer IE

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