30 Publications (Page 1 of 2)
2017
Frontotemporal Dementia.
Olney, Nicholas T⋅Spina, Salvatore and Miller, Bruce L
Neurologic clinics, vol. 35, (no. 2), pp. 339-374, May 2017. | Journal Article
2015
Frontotemporal dementia
Bang, Jee⋅Spina, Salvatore and Miller, Bruce
The Lancet, vol. 386, (no. 10004), pp. 1672-1682, Oct 24, 2015. | Journal Article
 
Frontotemporal dementia.
Bang, Jee⋅Spina, Salvatore and Miller, Bruce L
Lancet (London, England), vol. 386, (no. 10004), pp. 1672-1682, October 24, 2015. | Journal Article
2014
Visuoperception test predicts pathologic diagnosis of Alzheimer disease in corticobasal syndrome.
Boyd, Clara⋅Boyd, Clara D⋅Boyd, Clara D⋅Tierney, Michael⋅Tierney, Michael⋅Tierney, Michael⋅Wassermann, Eric⋅Wassermann, Eric⋅Wassermann, Eric M⋅Spina, Salvatore⋅Spina, Salvatore⋅Spina, Salvatore⋅Oblak, Adrian L⋅Oblak, Adrian⋅Oblak, Adrian L⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Grafman, Jordan H⋅Grafman, Jordan⋅Grafman, Jordan⋅Huey, Edward⋅Huey, Edward and Huey, Edward
Neurology, vol. 83, (no. 6), pp. 510-9, 2014/Aug/5. | Journal Article
2013
Parkinsonian features in hereditary diffuse leukoencephalopathy with spheroids (HDLS) and CSF1R mutations.
Sundal, Christina⋅Fujioka, Shinsuke⋅Van Gerpen, Jay A⋅Wider, Christian⋅Nicholson, Alexandra M⋅Baker, Matt⋅Shuster, Elizabeth A⋅Aasly, Jan⋅Spina, Salvatore⋅Ghetti, Bernardino⋅Roeber, Sigrun⋅Garbern, James⋅Tselis, Alex⋅Swerdlow, Russell H⋅Miller, Bradley B⋅Borjesson-Hanson, Anne⋅Uitti, Ryan J⋅Ross, Owen A⋅Stoessl, A J⋅Rademakers, Rosa⋅Josephs, Keith A⋅Dickson, Dennis W⋅Broderick, Daniel and Wszolek, Zbigniew K
Parkinsonism & related disorders, vol. 19, (no. 10), pp. 869-77, 2013/Oct. | Journal Article
 
Phenotypic variability in three families with valosin-containing protein mutation.
Spina, Salvatore⋅S, Spina⋅Van Laar, A D⋅AD, Van Laar⋅Murrell, Jill R⋅JR, Murrell⋅Hamilton, Ronald L⋅RL, Hamilton⋅JK, Kofler⋅Kofler, Julia⋅Epperson, F⋅F, Epperson⋅MR, Farlow⋅Farlow, Martin R⋅OL, Lopez⋅Lopez, Oscar⋅Quinlan, J⋅J, Quinlan⋅Dekosky, Steven T⋅ST, DeKosky⋅B, Ghetti and Ghetti, Bernardino
European journal of neurology : the official journal of the European Federation of Neurological Societies, vol. 20, (no. 2), pp. 251-8, 2013/Feb. | Journal Article
2012
Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
Lunetta, Kathryn⋅Barmada, Michael⋅Coppola, Giovanni⋅Stern, Robert⋅Chinnathambi, Subashchandrabose⋅Lee, Jason J⋅Dombroski, Beth A⋅Baker, Matt C⋅Soto-Ortolaza, Alexandra I⋅Lee, Suzee E⋅Klein, Eric⋅Huang, Alden Y⋅Sears, Renee⋅Lane, Jessica R⋅Karydas, Anna M⋅Kenet, Robert O⋅Biernat, Jacek⋅Wang, Li San⋅Cotman, Carl W⋅Decarli, Charles S⋅Levey, Allan I⋅Ringman, John M⋅Mendez, Mario F⋅Chui, Helena C⋅Le Ber, Isabelle⋅Brice, Alexis⋅Lupton, Michelle K⋅Preza, Elisavet⋅Lovestone, Simon⋅Powell, John F⋅Graff-Radford, Neill⋅Petersen, Ronald C⋅Boeve, Bradley F⋅Lippa, Carol F⋅Bigio, Eileen H⋅Mackenzie, Ian⋅Finger, Elizabeth⋅Kertesz, Andrew⋅Caselli, Richard J⋅Gearing, Marla⋅Juncos, Jorge L⋅Ghetti, Bernardino⋅Spina, Salvatore⋅Bordelon, Yvette⋅Tourtellotte, Wallace W⋅Frosch, Matthew P⋅Vonsattel, Jean P⋅Zarow, Chris⋅Beach, Thomas G⋅Albin, Roger L⋅Lieberman, Andrew P⋅Lee, Virginia M⋅Trojanowski, John Q⋅Van Deerlin, Vivianna⋅Bird, Thomas D⋅Galasko, Douglas R⋅Masliah, Eliezer⋅White, Charles L⋅Troncoso, Juan C⋅Hannequin, Didier⋅Boxer, Adam L⋅Geschwind, Michael D⋅Kumar, Satish⋅Mandelkow, Eva-Maria⋅Wszolek, Zbigniew K⋅Uitti, Ryan J⋅Dickson, Dennis W⋅Haines, Jonathan L⋅Mayeux, Richard⋅Vance, Jeffery M⋅Farrer, Lindsay⋅Ross, Owen A⋅Rademakers, Rosa⋅Schellenberg, Gerard D⋅Miller, Bruce L⋅Mandelkow, Eckhard and Geschwind, Daniel
Human molecular genetics, vol. 21, (no. 15), pp. 3500-12, 2012/Aug/1. | Journal Article
 
MRI characteristics and scoring in HDLS due to CSF1R gene mutations.
Sundal, Christina⋅Van Gerpen, Jay A⋅Nicholson, Alexandra M⋅Wider, Christian⋅Shuster, Elizabeth A⋅Aasly, Jan⋅Spina, Salvatore⋅Ghetti, Bernardino⋅Roeber, Sigrun⋅Garbern, James⋅Borjesson-Hanson, Anne⋅Tselis, Alex⋅Swerdlow, Russell H⋅Miller, Bradley B⋅Fujioka, Shinsuke⋅Heckman, Michael G⋅Uitti, Ryan J⋅Josephs, Keith A⋅Baker, Matt⋅Andersen, Oluf⋅Rademakers, Rosa⋅Dickson, Dennis W⋅Broderick, Daniel and Wszolek, Zbigniew K
Neurology, vol. 79, (no. 6), pp. 566-74, 2012/Aug/7. | Journal Article
 
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
Rademakers, Rosa⋅Baker, Matt⋅Nicholson, Alexandra M⋅Rutherford, Nicola J⋅Finch, NiCole⋅Soto-Ortolaza, Alexandra⋅Lash, Jennifer⋅Wider, Christian⋅Wojtas, Aleksandra⋅DeJesus-Hernandez, Mariely⋅Adamson, Jennifer⋅Kouri, Naomi⋅Sundal, Christina⋅Shuster, Elizabeth A⋅Aasly, Jan⋅MacKenzie, James⋅Roeber, Sigrun⋅Kretzschmar, Hans A⋅Boeve, Bradley F⋅Knopman, David S⋅Petersen, Ronald C⋅Cairns, Nigel⋅Ghetti, Bernardino⋅Spina, Salvatore⋅Garbern, James⋅Tselis, Alexandros C⋅Uitti, Ryan⋅Das, Pritam⋅Van Gerpen, Jay A⋅Meschia, James F⋅Levy, Shawn⋅Broderick, Daniel F⋅Graff-Radford, Neill⋅Ross, Owen A⋅Miller, Bradley B⋅Swerdlow, Russell H⋅Dickson, Dennis W and Wszolek, Zbigniew K
Nature Genetics, vol. 44, (no. 2), pp. 200-5, Feb 2012. | Journal Article
2011
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.
Naj, Adam C⋅Naj, Adam C⋅AC, Naj⋅...⋅G, Jun⋅Jun, Gyungah⋅Jun, Gyungah⋅Beecham, Gary W⋅Beecham, Gary⋅GW, Beecham⋅Wang, Li-San⋅Wang, Li San⋅LS, Wang⋅Vardarajan, Badri N⋅Vardarajan, Badri Narayan⋅BN, Vardarajan⋅J, Buros⋅Buros, Jacqueline⋅Buros, Jacqueline⋅Gallins, Paul J⋅PJ, Gallins⋅Gallins, Paul J⋅Buxbaum, Joseph D⋅JD, Buxbaum⋅Buxbaum, Joseph D⋅Jarvik, Gail P⋅GP, Jarvik⋅Jarvik, Gail P⋅Crane, Paul⋅Crane, Paul K⋅PK, Crane⋅Larson, Eric B⋅Larson, Eric B⋅EB, Larson⋅Bird, Thomas D⋅Bird, Thomas D⋅TD, Bird⋅BF, Boeve⋅Boeve, Bradley F⋅Boeve, Bradley F⋅GD, Schellenberg⋅Graff-Radford, Neill R⋅Graff-Radford, Neill R⋅De Jager, Philip L⋅De Jager, Philip⋅Evans, Denis A⋅Evans, Denis⋅Schneider, Julie A⋅Schneider, Julie A⋅Carrasquillo, Minerva M⋅Carrasquillo, Minerva M⋅Ertekin-Taner, Nilufer⋅Ertekin-Taner, Nilufer⋅Younkin, Steven G⋅Younkin, Steven G⋅Cruchaga, Carlos⋅Cruchaga, Carlos⋅Kauwe, John S⋅Kauwe, John S K⋅Nowotny, Petra⋅Nowotny, Petra⋅Kramer, Patricia⋅Kramer, Patricia L⋅Hardy, John⋅Hardy, John⋅Huentelman, Matthew J⋅Huentelman, Matthew J⋅Myers, Amanda J⋅Myers, Amanda⋅Barmada, M. M⋅Barmada, Michael M⋅Demirci, F Yesim⋅Demirci, F. Y⋅Baldwin, Clint⋅Baldwin, Clinton T⋅Green, Robert C⋅Green, Robert C⋅Rogaeva, Ekaterina⋅Rogaeva, Ekaterina⋅George-Hyslop, P.S.⋅St. George Hyslop, Peter⋅St George-Hyslop, Peter⋅St George-Hyslop, Peter⋅Arnold, Steven E⋅Arnold, Steven E⋅Barber, Robert⋅Barber, Robert⋅Beach, Thomas⋅Beach, Thomas⋅Bigio, Eileen H⋅Bigio, Eileen H⋅Bowen, James D⋅Bowen, James⋅Boxer, Adam⋅Boxer, Adam L⋅Burke, James R⋅Burke, James R⋅Cairns, Nigel J⋅Cairns, Nigel J⋅Carlson, Chris S⋅Carlson, Christopher⋅Carney, Regina M⋅Carney, Regina M⋅Carroll, Steven L⋅Carroll, Stephen L⋅Chui, Helena C⋅Chui, Helena C⋅Clark, David G⋅Clark, David G⋅Corneveaux, Jason⋅Corneveaux, Jason J⋅Cotman, Carl W⋅Cotman, Carl W⋅Cummings, Jeffrey L⋅Cummings, Jeffrey L⋅DeCarli, Charles⋅Decarli, C.⋅De Carli, Charles D⋅DeKosky, Steven T⋅Dekosky, Steven T⋅DeKosky, Steven T⋅Diaz-Arrastia, Ramon⋅Diaz Arrastia, Ramon R⋅Dick, Malcolm⋅Dick, Malcolm⋅Dickson, Dennis W⋅Dickson, Dennis W⋅Ellis, W. G⋅Ellis, William G⋅Faber, Kelley M⋅Faber, Kelley M⋅Fallon, Kenneth B⋅Fallon, Kenneth B⋅Farlow, Martin R⋅Farlow, Martin R⋅Ferris, Steven H⋅Ferris, Steven⋅Frosch, Matthew P⋅Frosch, Matthew P⋅Galasko, Douglas R⋅Galasko, Douglas R⋅Ganguli, Mary⋅Ganguli, Mary M⋅Gearing, Marla⋅Gearing, Marla⋅Geschwind, Daniel H⋅Geschwind, Daniel⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Gilbert, John R⋅Gilbert, John R⋅Gilman, Sid⋅Gilman, Sid⋅Giordani, Bruno⋅Giordani, Bruno J⋅Glass, Jonathan D⋅Glass, Jonathan D⋅Growdon, John H⋅Growdon, John H⋅Hamilton, Ronald L⋅Hamilton, Ronald L⋅Harrell, Lindy E⋅Harrell, Lindy E⋅Head, Elizabeth⋅Head, Elizabeth⋅Honig, Lawrence S⋅Honig, Lawrence S⋅Hulette, Christine M⋅Hulette, Christine M⋅Hyman, Bradley T⋅Hyman, Bradley T⋅Jicha, Gregory A⋅Jicha, Gregory⋅Jin, Lee Way⋅Jin, Lee-Way⋅Johnson, Nancy⋅Johnson, Nancy⋅Karlawish, Jason H⋅Karlawish, Jason⋅Karydas, Anna⋅Karydas, Anna⋅Kaye, Jeffrey A⋅Kaye, Jeff⋅Kim, Ronald⋅Kim, Ronald C⋅Koo, Edward H⋅Koo, Edward H⋅Kowall, Neil W⋅Kowall, Neil W⋅Lah, James J⋅Lah, James J⋅Levey, Allan I⋅Levey, Allan I⋅Lieberman, Andrew P⋅Lieberman, Andrew P⋅Lopez, Oscar⋅Lopez, Oscar L⋅Mack, Wendy J⋅Mack, Wendy J⋅MacK, W.J.⋅Marson, Daniel C⋅Marson, Daniel C⋅Martiniuk, Frank⋅Martiniuk, Frank T⋅Mash, Deborah C⋅Mash, Deborah C⋅Masliah, Eliezer⋅Masliah, Eliezer⋅McCormick, Wayne C⋅McCormick, Wayne C⋅Mccormick, Wayne C⋅Mc Curry, Susan M⋅McCurry, Susan M⋅McDavid, Andrew N⋅McDavid, Andrew N⋅Mc Kee, Ann⋅McKee, Ann C⋅Mesulam, Marek Marsel M⋅Mesulam, Marsel⋅Miller, Bruce L⋅Miller, Bruce L⋅Miller, Carol A⋅Miller, Joshua⋅Parisi, Joseph E⋅Perl, Daniel P⋅Peskind, Elaine R⋅Petersen, Ronald C⋅Poon, Wayne W⋅Quinn, Joseph F⋅Rajbhandary, Ruchita A⋅Raskind, Murray⋅Reisberg, Barry⋅Ringman, John M⋅Roberson, Erik⋅Rosenberg, R. N⋅Sano, Mary⋅Schneider, Lon S⋅Seeley, William W⋅Shelanski, Michael L⋅Slifer, Michael A⋅Smith, Charles⋅Sonnen, Joshua⋅Spina, Salvatore⋅Stern, Robert A⋅Tanzi, Rudy E⋅Trojanowski, John Q⋅Troncoso, Juan C⋅Van Deerlin, Vivianna⋅Vinters, Harry V⋅Vonsattel, Jean Paul⋅Weintraub, Sandra⋅Welsh Bohmer, Kathleen A⋅Williamson, Jennifer⋅Woltjer, Randall L⋅Cantwell, Laura B⋅Dombroski, Beth A⋅Beekly, Duane⋅Lunetta, Kathryn L⋅Martin, Eden R⋅Kamboh, M. I⋅Saykin, Andrew⋅Reiman, Eric M⋅Bennett, David A⋅Morris, John C⋅Montine, Thomas J⋅Goate, Alison⋅Blacker, Deborah L⋅Tsuang, Debby W⋅Hakonarson, Hakon⋅Kukull, Walter A⋅Foroud, Tatiana M⋅Haines, Jonathan L⋅Mayeux, Richard⋅Vance, Jeffery M⋅Pericak-Vance, Margaret A⋅Farrer, Lindsay and Schellenberg, Gerard D
Nature genetics, vol. 43, (no. 5), pp. 436-41, 2011/May. | Journal Article
 
Genetic and Clinical Features of Progranulin-Associated Frontotemporal Lobar Degeneration
Chen-Plotkin, Alice S⋅Chen-Plotkin, A.S.⋅Martinez-Lage, Maria⋅Martinez-Lage, M.⋅Sleiman, P.M.A.⋅Sleiman, Patrick M⋅Hu, W.⋅Hu, William⋅Greene, Robert⋅Greene, R.⋅Wood, Elisabeth M⋅Wood, E.M.⋅Bing, Shaoxu⋅Bing, S.⋅Grossman, Murray⋅Grossman, M.⋅Schellenberg, G.D.⋅Schellenberg, Gerard D⋅Hatanpaa, K.J.⋅Hatanpaa, Kimmo J⋅Weiner, Myron⋅Weiner, M.F.⋅White III, C.L.⋅White, Charles L⋅Brooks, William⋅Brooks, W.S.⋅Halliday, G.M.⋅Halliday, Glenda M⋅Kril, Jillian⋅Kril, J.J.⋅Gearing, M.⋅Gearing, Marla⋅Beach, T.G.⋅Beach*, Thomas G⋅Graff-Radford, N.R.⋅Graff*-Radford, Neill R⋅Dickson, D.W.⋅Dickson, Dennis W⋅Rademakers, Rosa⋅Rademakers, R.⋅Boeve, Bradley F⋅Boeve, B.F.⋅Pickering-Brown, Stuart⋅Pickering-Brown, S.M.⋅Snowden, J.⋅Snowden, Julie⋅van Swieten, John C⋅Van Swieten, J.C.⋅Heutink, Peter⋅Heutink, P.⋅Seelaar, H.⋅Seelaar, Harro⋅Murrell, J.R.⋅Murrell, Jill R⋅Ghetti, Bernardino⋅Ghetti, B.⋅Spina, Salvatore⋅Spina, S.⋅Grafman, Jordan⋅Grafman, J.⋅Kaye, J.A.⋅Kaye, Jeff⋅Woltjer, Randall L⋅Woltjer, R.L.⋅Mesulam, M.⋅Mesulam, Marek Marsel M⋅Bigio, E.⋅Bigio, Eileen H⋅Lladó, A.⋅Llado, Albert⋅Miller, B.L.⋅Miller, Bruce L⋅Alzualde, Ainhoa⋅Alzualde, A.⋅Moreno, F.⋅Moreno, Fermin⋅Rohrer, Jonathan D⋅Rohrer, J.D.⋅Mackenzie, I.R.A.⋅Mackenzie, Ian⋅Feldman, H.H.⋅Feldman, Howard⋅Hamilton, R.L.⋅Hamilton, Ronald L⋅Cruts, M.⋅Cruts, Marc⋅Engelborghs, S.⋅Engelborghs, Sebastiaan⋅De Deyn, P.P.⋅De Deyn, Peter P⋅Van Broeckhoven, Christine⋅Van Broeckhoven, C.⋅Bird, Thomas D⋅Bird, T.D.⋅Cairns, Nigel⋅Cairns, N.J.⋅Goate, A.⋅Goate, Alison⋅Frosch, Matthew P⋅Frosch, M.P.⋅Riederer, Peter F⋅Riederer, P.F.⋅Bogdanovic, Nenad⋅Bogdanovic, N.⋅Lee, Virginia M⋅Lee, V.M.Y.⋅Trojanowski, J.Q.⋅Trojanowski, John Q⋅Van Deerlin, V.M. and Van Deerlin, Vivianna
Archives of Neurology, vol. 68, (no. 4), pp. 488-497, 2011. | Journal Article
 
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy
Höglinger, G.U.⋅Höglinger, G.U.⋅Höglinger, Günter U⋅Melhem, N.M.⋅Melhem, N.M.⋅Melhem, Nadine⋅Dickson, Dennis W⋅Dickson, D.W.⋅Dickson, D.W.⋅Sleiman, P.M.A.⋅Sleiman, P.M.A.⋅Sleiman, Patrick M⋅Wang, L.-S.⋅Wang, L.-S.⋅Wang, Li San⋅Klei, L.⋅Klei, Lambertus⋅Klei, L.⋅Rademakers, R.⋅Rademakers, Rosa⋅Rademakers, R.⋅De Silva, R.⋅De Silva, R.⋅De Silva, Rohan⋅Litvan, I.⋅Litvan, I.⋅Litvan, Irene⋅Riley, David E⋅Riley, D.E.⋅Riley, D.E.⋅Van Swieten, J.C.⋅van Swieten, John C⋅Van Swieten, J.C.⋅Heutink, P.⋅Heutink, P.⋅Heutink, Peter⋅Wszolek, Z.K.⋅Wszolek, Z.K.⋅Wszolek, Zbigniew K⋅Uitti, Ryan J⋅Uitti, R.J.⋅Uitti, R.J.⋅Vandrovcova, J.⋅Vandrovcova, Jana⋅Vandrovcova, J.⋅Hurtig, H.I.⋅Hurtig, Howard I⋅Hurtig, H.I.⋅Gross, R.G.⋅Gross, R.G.⋅Gross, Rachel G⋅Maetzler, W.⋅Maetzler, Walter⋅Maetzler, W.⋅Goldwurm, Stefano⋅Goldwurm, S.⋅Goldwurm, S.⋅Tolosa, E.⋅Tolosa, Eduardo⋅Tolosa, E.⋅Borroni, B.⋅Borroni, B.⋅Borroni, Barbara⋅Pastor, P.⋅Pastor, P.⋅Pastor, Pau⋅Cantwell, L.B.⋅Cantwell, Laura B⋅Cantwell, L.B.⋅Han, Mi R⋅Han, M.R.⋅Han, M.R.⋅Dillman, Allissa⋅Dillman, A.⋅Dillman, A.⋅van der Brug, Marcel P⋅Van Der Brug, M.P.⋅Van Der Brug, M.P.⋅Gibbs, J. 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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids.
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Rapidly progressive atypical parkinsonism associated with frontotemporal lobar degeneration and motor neuron disease
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Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
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Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update
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Association of ideomotor apraxia with frontal gray matter volume loss in corticobasal syndrome.
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Failure to detect the presence of prions in the uterine and gestational tissues from a Gravida with Creutzfeldt-Jakob disease.
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The American journal of pathology, vol. 174, (no. 5), pp. 1602-8, 2009/May. | Journal Article
 
Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations
Mackenzie, Ian R A⋅Mackenzie, Ian⋅Neumann, Manuela⋅Neumann, Manuela⋅Bigio, Eileen H⋅Bigio, Eileen H⋅Cairns, Nigel J⋅Cairns, Nigel⋅Alafuzoff, Irina⋅Alafuzoff, Irina⋅Kril, Jillian⋅Kril, Jillian⋅Kovacs, Gabor G⋅Kovacs, Gabor G⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Halliday, Glenda M⋅Halliday, Glenda⋅Holm, Ida E⋅Holm, Ida E⋅Ince, Paul G⋅Ince, Paul G⋅Kamphorst, Wouter⋅Kamphorst, Wouter⋅Revesz, Tamas⋅Revesz, Tamas⋅Rozemuller, Annemieke J M⋅Rozemuller, Annemieke J⋅Kumar-Singh, Samir⋅Kumar-Singh, Samir⋅Akiyama, Haruhiko⋅Akiyama, Haruhiko⋅Baborie, Atik⋅Baborie, Atik⋅Spina, Salvatore⋅Spina, Salvatore⋅Dickson, Dennis W⋅Dickson, Dennis W⋅Trojanowski, John Q⋅Trojanowski, John Q⋅Mann, David M A and Mann, David
Acta Neuropathologica, vol. 117, (no. 1), pp. 15-18, 2009. | Journal Article
 
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea
Kovacs, Gabor G⋅Murrell, Jill R⋅Horvath, Sandor⋅Haraszti, Laszlo⋅Majtenyi, Katalin⋅Molnar, Maria J⋅Budkadhc, Herbert⋅Ghetti, Bernardino and Spina, Salvatore
Movement Disorders, vol. 24, (no. 12), pp. 1842-1847, 2009. | Journal Article
 
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
Kovacs, Gabor G⋅Kovacs, Gabor G⋅Kovacs, Gabor G⋅Murrell, Jill R⋅Murrell, Jill R⋅Murrell, Jill R⋅Horvath, Sandor⋅Horvath, Sandor⋅Horvath, Sandor⋅Haraszti, Laszlo⋅Haraszti, Laszlo⋅Haraszti, Laszlo⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Molnar, Maria J⋅Molnar, Maria J⋅Molnar, Maria J⋅Budka, Herbert⋅Budka, Herbert⋅Budka, Herbert⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Ghetti, Bernardino⋅Spina, Salvatore⋅Spina, Salvatore and Spina, Salvatore
Movement disorders : official journal of the Movement Disorder Society, vol. 24, (no. 12), pp. 1843-7, 2009/Sep/15. | Journal Article
2008
The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family
Spina, Salvatore⋅Spina, Salvatore⋅Farlow, Martin R⋅Farlow, Martin R⋅Unverzagt, Frederick W⋅Unverzagt, Frederick⋅Kareken, David A⋅Kareken, David A⋅Murrell, Jill R⋅Murrell, Jill R⋅Fraser, Graham⋅Fraser, Graham⋅Epperson, Francine⋅Epperson, Francine⋅Crowther, R Anthony⋅Crowther, RAnthony⋅Spillantini, Maria G⋅Spillantini, Maria G⋅Goedert, Michel⋅Goedert, Michel⋅Ghetti, Bernardino and Ghetti, Bernardino
Brain, vol. 131, (no. 1), pp. 72-89, 2008. | Journal Article
 
White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration.
Kovacs, Gabor G⋅Kovacs, Gabor G⋅Majtenyi, Katalin⋅Majtenyi, Katalin⋅Spina, Salvatore⋅Spina, Salvatore⋅Murrell, Jill R⋅Murrell, Jill R⋅Gelpi, Ellen⋅Gelpi, Ellen⋅Hoftberger, Romana⋅Hoftberger, Romana⋅Fraser, Graham⋅Fraser, Graham⋅Crowther, R A⋅Crowther, R A⋅Goedert, Michel⋅Goedert, Michel⋅Budka, Herbert⋅Budka, Herbert⋅Ghetti, Bernardino and Ghetti, Bernardino
Journal of neuropathology and experimental neurology, vol. 67, (no. 10), pp. 963-75, 2008/Oct. | Journal Article
2007
Clinicopathologic features of frontotemporal dementia with Progranulin sequence variation
Spina, Salvatore⋅Murrell, Jill R⋅Huey, ED⋅Wassermann, Eric⋅Pietrini, Pietro⋅Baraibar, MA⋅Barbeito, AG⋅Troncoso, Juan C⋅Vidal, Ruben G⋅Ghetti, Bernardino and Grafman, Jordan
Neurology, vol. 68, (no. 11), pp. 820-827, 2007. | Journal Article