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2017
Ranasinghe KG, Gill JS, Kothare H, Beagle AJ, Mizuiri D, Honma SM, Gorno-Tempini MLuisa, Miller BL, Vossel KA, Nagarajan SS et al..  2017.  Abnormal vocal behavior predicts executive and memory deficits in Alzheimer's disease.. Neurobiol Aging. 52:71-80.
Carlomagno Y, Chung D-EChloe, Yue M, Castanedes-Casey M, Madden BJ, Dunmore J, Tong J, DeTure M, Dickson DW, Petrucelli L et al..  2017.  An acetylation-phosphorylation switch that regulates tau aggregation propensity and function.. J Biol Chem. 292(37):15277-15286.
Perry DC, Brown JA, Possin KL, Datta S, Trujillo A, Radke A, Karydas A, Kornak J, Sias AC, Rabinovici GD et al..  2017.  Clinicopathological correlations in behavioural variant frontotemporal dementia.. Brain. 140(12):3329-3345.
Possin KL, Kim H, Geschwind MD, Moskowitz T, Johnson ET, Sha SJ, Apple A, Xu D, Miller BL, Finkbeiner S et al..  2017.  Egocentric and allocentric visuospatial working memory in premotor Huntington's disease: A double dissociation with caudate and hippocampal volumes.. Neuropsychologia. 101:57-64.
Lisi V, Singh B, Giroux M, Guzman E, Painter MW, Cheng Y-C, Huebner E, Coppola G, Costigan M, Woolf CJ et al..  2017.  Enhanced Neuronal Regeneration in the CAST/Ei Mouse Strain Is Linked to Expression of Differentiation Markers after Injury.. Cell Rep. 20(5):1136-1147.
Spina S, Schonhaut DR, Boeve BF, Seeley WW, Ossenkoppele R, O'Neil JP, Lazaris A, Rosen HJ, Boxer AL, Perry DC et al..  2017.  Frontotemporal dementia with the V337M mutation: Tau-PET and pathology correlations.. Neurology. 88(8):758-766.
Chen J, Yu J-T, Wojta K, Wang H-F, Zetterberg H, Blennow K, Yokoyama JS, Weiner MW, Kramer JH, Rosen H et al..  2017.  Genome-wide association study identifies locus influencing human plasma tau levels.. Neurology. 88(7):669-676.
Olney NT, Alquezar C, Ramos EMarisa, Nana AL, Fong JC, Karydas AM, Taylor JB, Stephens ML, Argouarch AR, Van Berlo VA et al..  2017.  Linking tuberous sclerosis complex, excessive mTOR signaling, and age-related neurodegeneration: a new association between TSC1 mutation and frontotemporal dementia.. Acta Neuropathol. 134(5):813-816.
Theofilas P, Ehrenberg AJ, Dunlop S, Alho ATDi Loren, Nguy A, Leite RElaine Par, Rodriguez RDiehl, Mejia MB, Suemoto CK, Ferretti-Rebustini REloah De L et al..  2017.  Locus coeruleus volume and cell population changes during Alzheimer's disease progression: A stereological study in human postmortem brains with potential implication for early-stage biomarker discovery.. Alzheimers Dement. 13(3):236-246.
Krabbe G, S Minami S, Etchegaray JI, Taneja P, Djukic B, Davalos D, Le D, Lo I, Zhan L, Reichert MC et al..  2017.  Microglial NFκB-TNFα hyperactivation induces obsessive-compulsive behavior in mouse models of progranulin-deficient frontotemporal dementia.. Proc Natl Acad Sci U S A. 114(19):5029-5034.
Pressman PS, Simpson M, Gola K, Shdo SM, Spinelli EG, Miller BL, Gorno-Tempini MLuisa, Rankin K, Levenson RW.  2017.  Observing conversational laughter in frontotemporal dementia.. J Neurol Neurosurg Psychiatry. 88(5):418-424.
Huang AY, Yu D, Davis LK, Sul JHoon, Tsetsos F, Ramensky V, Zelaya I, Ramos EMarisa, Osiecki L, Chen JA et al..  2017.  Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.. Neuron. 94(6):1101-1111.e7.
Yokoyama JS, Marx G, Brown JA, Bonham LW, Wang D, Coppola G, Seeley WW, Rosen HJ, Miller BL, Kramer JH et al..  2017.  Systemic klotho is associated with KLOTHO variation and predicts intrinsic cortical connectivity in healthy human aging.. Brain Imaging Behav. 11(2):391-400.
Vitte J, Gao F, Coppola G, Judkins AR, Giovannini M.  2017.  Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development.. Nat Commun. 8(1):300.
Liu CY, Ohki Y, Tomita T, Osawa S, Reed BR, Jagust W, Van Berlo V, Jin L-W, Chui HC, Coppola G et al..  2017.  Two Novel Mutations in the First Transmembrane Domain of Presenilin1 Cause Young-Onset Alzheimer's Disease.. J Alzheimers Dis. 58(4):1035-1041.
2016
Mandelli MLuisa, Vilaplana E, Brown JA, H Hubbard I, Binney RJ, Attygalle S, Santos-Santos MA, Miller ZA, Pakvasa M, Henry ML et al..  2016.  Healthy brain connectivity predicts atrophy progression in non-fluent variant of primary progressive aphasia.. Brain. 139(Pt 10):2778-2791.
Dutt S, Binney RJ, Heuer HW, Luong P, Attygalle S, Bhatt P, Marx GA, Elofson J, Tartaglia MC, Litvan I et al..  2016.  Progression of brain atrophy in PSP and CBS over 6 months and 1 year.. Neurology. 87(19):2016-2025.
Sirkis DW, Bonham LW, Aparicio RE, Geier EG, Ramos EMarisa, Wang Q, Karydas A, Miller ZA, Miller BL, Coppola G et al..  2016.  Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression.. Acta Neuropathol Commun. 4(1):98.
Alho ATereza Di, Suemoto CKimie, Polichiso L, Tampellini E, de Oliveira KCristina, Molina M, Santos GAparecida, Nascimento C, Leite RElaine Par, Ferreti-Rebustini REloah de L et al..  2016.  Three-dimensional and stereological characterization of the human substantia nigra during aging.. Brain Struct Funct. 221(7):3393-403.
Soosman SK, Joseph-Mathurin N, Braskie MN, Bordelon YM, Wharton D, Casado M, Coppola G, McCallum H, Nuwer M, Coutin-Churchman P et al..  2016.  Widespread white matter and conduction defects in PSEN1-related spastic paraparesis.. Neurobiol Aging. 47:201-209.