Clinical Observations and Neuropathology of Rabbits in the Acute Stages of Type 2 Herpes Simplex Infections

Por Halter, S. A., Barnett, R. I., Smith, J. E., Romero-Sierra, C.
Publicado em 1973

Clinical Correlates of Depressive Symptoms in Familial Parkinson's Disease

Por Pankratz, Nathan, Marder, Karen S., Halter, Cheryl A., Rudolph, Alice, Shults, Cliff W., Nichols, William C., Foroud, Tatiana
Publicado em 2008

Distinctive patterns of hyperplasia in transgenic mice with mouse mammary tumor virus transforming growth factor-alpha. Characterization of mammary gland and skin proliferations.

Por Halter, S. A., Dempsey, P., Matsui, Y., Stokes, M. K., Graves-Deal, R., Hogan, B. L., Coffey, R. J.
Publicado em 1992

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

Por Pankratz, N, Kissell, D K., Pauciulo, M W., Halter, C A., Rudolph, A, Pfeiffer, R F., Marder, K S., Foroud, T, Nichols, W C.
Publicado em 2009

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

Por Simon, David K, Pankratz, Nathan, Kissell, Diane K, Pauciulo, Michael W, Halter, Cheryl A, Rudolph, Alice, Pfeiffer, Ronald F, Nichols, William C, Foroud, Tatiana
Publicado em 2010

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

Por Nichols, W C., Pankratz, N, Marek, D K., Pauciulo, M W., Elsaesser, V E., Halter, C A., Rudolph, A, Wojcieszek, J, Pfeiffer, R F., Foroud, T
Publicado em 2009

Synergistic interaction of the Neu proto-oncogene product and transforming growth factor alpha in the mammary epithelium of transgenic mice.

Por Muller, W J, Arteaga, C L, Muthuswamy, S K, Siegel, P M, Webster, M A, Cardiff, R D, Meise, K S, Li, F, Halter, S A, Coffey, R J
Publicado em 1996

Alpha-Synuclein and Familial Parkinson’s Disease

Por Pankratz, Nathan, Nichols, William C., Elsaesser, Veronika E., Pauciulo, Michael W., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Pfeiffer, Ronald F., Foroud, Tatiana
Publicado em 2009

Mutations in DJ-1 are rare in familial Parkinson disease

Por Pankratz, Nathan, Pauciulo, Michael W., Elsaesser, Veronika E., Marek, Diane K., Halter, Cheryl A., Wojcieszek, Joanne, Rudolph, Alice, Shults, Clifford W., Foroud, Tatiana, Nichols Ph.D., William C.
Publicado em 2006

Variation in GIGYF2 is not associated with Parkinson disease

Por Nichols, W C., Kissell, D K., Pankratz, N, Pauciulo, M W., Elsaesser, V E., Clark, K A., Halter, C A., Rudolph, A, Wojcieszek, J, Pfeiffer, R F., Foroud, T
Publicado em 2009

Kirsten ras mutations in patients with colorectal cancer: the ‘RASCAL II’ study

Por Andreyev, H J N, Norman, A R, Cunningham, D, Oates, J, Dix, B R, Iacopetta, B J, Young, J, Walsh, T, Ward, R, Hawkins, N, Beranek, M, Jandik, P, Benamouzig, R, Jullian, E, Laurent-Puig, P, Olschwang, S, Muller, O, Hoffmann, I, Rabes, H M, Zietz, C, Troungos, C, Valavanis, C, Yuen, S T, Ho, J W C, Croke, C T, O'Donoghue, D P, Giaretti, W, Rapallo, A, Russo, A, Bazan, V, Tanaka, M, Omura, K, Azuma, T, Ohkusa, T, Fujimori, T, Ono, Y, Pauly, M, Faber, C, Glaesener, R, Goeij, A F P M de, Arends, J W, Andersen, S N, Lövig, T, Breivik, J, Gaudernack, G, Clausen, O P F, Angelis, P De, Meling, G I, Rognum, T O, Smith, R, Goh, H-S, Font, A, Rosell, R, Sun, X F, Zhang, H, Benhattar, J, Losi, L, Lee, J Q, Wang, S T, Clarke, P A, Bell, S, Quirke, P, Bubb, V J, Piris, J, Cruickshank, N R, Morton, D, Fox, J C, Al-Mulla, F, Lees, N, Hall, C N, Snary, D, Wilkinson, K, Dillon, D, Costa, J, Pricolo, V E, Finkelstein, S D, Thebo, J S, Senagore, A J, Halter, S A, Wadler, S, Malik, S, Krtolica, K, Urosevic, N
Publicado em 2001