Longitudinal modeling of frontal cognition in APOE ε4 homozygotes, heterozygotes, and noncarriers

Por Caselli, R.J., Dueck, A.C., Locke, D.E.C., Hoffman-Snyder, C.R., Woodruff, B.K., Rapcsak, S.Z., Reiman, E.M.
Publicado em 2011

CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms

Por Scala, E, Ariani, F, Mari, F, Caselli, R, Pescucci, C, Longo, I, Meloni, I, Giachino, D, Bruttini, M, Hayek, G, Zappella, M, Renieri, A
Publicado em 2005

Brain and ventricular volumetric changes in frontotemporal lobar degeneration over 1 year

Por Knopman, D S., Jack, C R., Kramer, J H., Boeve, B F., Caselli, R J., Graff-Radford, N R., Mendez, M F., Miller, B L., Mercaldo, N D.
Publicado em 2009

Cerebrovascular risk factors and preclinical memory decline in healthy APOE ε4 homozygotes

Por Caselli, R.J., Dueck, A.C., Locke, D.E.C., Sabbagh, M.N., Ahern, G.L., Rapcsak, S.Z., Baxter, L.C., Yaari, R., Woodruff, B.K., Hoffman-Snyder, C., Rademakers, R., Findley, S., Reiman, E.M.
Publicado em 2011

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis–frontotemporal dementia phenotypes

Por Schymick, J C, Yang, Y, Andersen, P M, Vonsattel, J P, Greenway, M, Momeni, P, Elder, J, Chiò, A, Restagno, G, Robberecht, W, Dahlberg, C, Mukherjee, O, Goate, A, Graff‐Radford, N, Caselli, R J, Hutton, M, Gass, J, Cannon, A, Rademakers, R, Singleton, A B, Hardiman, O, Rothstein, J, Hardy, J, Traynor, B J
Publicado em 2007

Clinicopathologic correlations in 172 cases of rapid eye movement sleep behavior disorder with or without a coexisting neurologic disorder

Por Boeve, B.F., Silber, M.H., Ferman, T.J., Lin, S.C., Benarroch, E.E., Schmeichel, A.M., Ahlskog, J.E., Caselli, R.J., Jacobson, S., Sabbagh, M., Adler, C., Woodruff, B., Beach, T.G., Iranzo, A., Gelpi, E., Santamaria, J., Tolosa, E., Singer, C., Mash, D.C., Luca, C., Arnulf, I., Duyckaerts, C., Schenck, C.H., Mahowald, M.W., Dauvilliers, Y., Graff-Radford, N.R., Wszolek, Z.K., Parisi, J.E., Dugger, B., Murray, M.E., Dickson, D.W.
Publicado em 2013

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers

Por Finch, N., Carrasquillo, M.M., Baker, M., Rutherford, N.J., Coppola, G., DeJesus-Hernandez, M., Crook, R., Hunter, T., Ghidoni, R., Benussi, L., Crook, J., Finger, E., Hantanpaa, K.J., Karydas, A.M., Sengdy, P., Gonzalez, J., Seeley, W.W., Johnson, N., Beach, T.G., Mesulam, M., Forloni, G., Kertesz, A., Knopman, D.S., Uitti, R., White, C.L., Caselli, R., Lippa, C., Bigio, E.H., Wszolek, Z.K., Binetti, G., Mackenzie, I.R., Miller, B.L., Boeve, B.F., Younkin, S.G., Dickson, D.W., Petersen, R.C., Graff-Radford, N.R., Geschwind, D.H., Rademakers, R.
Publicado em 2011