Release of amyloid beta-protein precursor derivatives by electrical depolarization of rat hippocampal slices.

Por Nitsch, R M, Farber, S A, Growdon, J H, Wurtman, R J
Publicado em 1993

Segregation analysis reveals evidence of a major gene for Alzheimer disease.

Por Farrer, L A, Myers, R H, Connor, L, Cupples, L A, Growdon, J H
Publicado em 1991

Putamen–midbrain functional connectivity is related to striatal dopamine transporter availability in patients with Lewy body diseases

Por Rieckmann, A., Gomperts, S.N., Johnson, K.A., Growdon, J.H., Van Dijk, K.R.A.
Publicado no Neuroimage Clin (2015)

Evidence for a membrane defect in Alzheimer disease brain.

Por Nitsch, R M, Blusztajn, J K, Pittas, A G, Slack, B E, Growdon, J H, Wurtman, R J
Publicado em 1992

Multiple etiologies for Alzheimer disease are revealed by segregation analysis.

Por Rao, V. S., van Duijn, C. M., Connor-Lacke, L., Cupples, L. A., Growdon, J. H., Farrer, L. A.
Publicado em 1994

Brain amyloid and cognition in Lewy body diseases

Por Gomperts, S. N., Locascio, J. J., Marquie, M., Santarlasci, A. L., Rentz, D. M., Maye, J., Johnson, K. A., Growdon, J. H.
Publicado em 2012

Imaging amyloid deposition in Lewy body diseases

Por Gomperts, S N., Rentz, D M., Moran, E, Becker, J A., Locascio, J J., Klunk, W E., Mathis, C A., Elmaleh, D R., Shoup, T, Fischman, A J., Hyman, B T., Growdon, J H., Johnson, K A.
Publicado em 2008

Evidence for major gene inheritance of Alzheimer disease in families of patients with and without apolipoprotein E epsilon 4.

Por Rao, V. S., Cupples, A., van Duijn, C. M., Kurz, A., Green, R. C., Chui, H., Duara, R., Auerbach, S. A., Volicer, L., Wells, J., van Broeckhoven, C., Growdon, J. H., Haines, J. L., Farrer, L. A.
Publicado em 1996

Haplotypes and gene expression implicate the MAPT region for Parkinson disease: The GenePD Study

Por Tobin, J.E., Latourelle, J.C., Lew, M.F., Klein, C., Suchowersky, O., Shill, H.A., Golbe, L.I., Mark, M.H., Growdon, J.H., Wooten, G.F., Racette, B.A., Perlmutter, J.S., Watts, R., Guttman, M., Baker, K.B., Goldwurm, S., Pezzoli, G., Singer, C., Saint-Hilaire, M.H., Hendricks, A.E., Williamson, S., Nagle, M.W., Wilk, J.B., Massood, T., Laramie, J.M., DeStefano, A.L., Litvan, I., Nicholson, G., Corbett, A., Isaacson, S., Burn, D.J., Chinnery, P.F., Pramstaller, P.P., Sherman, S., Al-hinti, J., Drasby, E., Nance, M., Moller, A.T., Ostergaard, K., Roxburgh, R., Snow, B., Slevin, J.T., Cambi, F., Gusella, J.F., Myers, R.H.
Publicado em 2008

Specifically neuropathic Gaucher's mutations accelerate cognitive decline in Parkinson's

Por Liu, Ganqiang, Boot, Brendon, Locascio, Joseph J., Jansen, Iris E., Winder‐Rhodes, Sophie, Eberly, Shirley, Elbaz, Alexis, Brice, Alexis, Ravina, Bernard, van Hilten, Jacobus J., Cormier‐Dequaire, Florence, Corvol, Jean‐Christophe, Barker, Roger A., Heutink, Peter, Marinus, Johan, Williams‐Gray, Caroline H., Scherzer, Clemens R., Scherzer, C., Hyman, B.T., Ivinson, A.J., Trisini‐Lipsanopoulos, A., Franco, D., Burke, K., Sudarsky, L.R., Hayes, M.T., Umeh, C.C., Growdon, J.H., Schwarzschild, M.A., Hung, A.Y., Flaherty, A.W., Wills, A.‐M., Mejia, N.I., Gomperts, S.N., Khurana, V., Selkoe, D.J., Yi, T., Page, K., Liao, Z., Barker, R., Foltynie, T., Williams‐Gray, C.H., Mason, S., Winder‐Rhodes, S., Barker, R., Williams‐Gray, C.H., Breen, D., Cummins, G., Evans, J., Winder‐Rhodes, S., Corvol, J.‐C., Brice, A., Elbaz, A., Mallet, A., Vidailhet, M., Bonnet, A.‐M., Bonnet, C., Grabli, D., Hartmann, A., Klebe, S., Lacomblez, L., Mangone, G., Bourdain, F., Brandel, J.‐P., Derkinderen, P., Durif, F., Mesnage, V., Pico, F., Rascol, O., Forlani, S., Lesage, S., Tahiri, K., van Hilten, J.J., Marinus, J., Liao, Z., Page, K., Franco, D., Duong, K., Yi, T., Trisini‐Lipsanopoulos, A., Dong, X., Sudarsky, L.R., Hutten, S.J., Amr, S.S., Shoulson, I., Tanner, C.M., Lang, A.E., Nalls, M.A.
Publicado no Ann Neurol (2016)