Human hippocampus associates information in memory

Por Henke, Katharina, Weber, Bruno, Kneifel, Stefan, Wieser, Heinz Gregor, Buck, Alfred
Publicado em 1999

Non‐convulsive status epilepticus causing focal neurological deficits in CADASIL

Por Valko, Philipp O, Siccoli, Massimiliano M, Schiller, Andreas, Wieser, Heinz‐Gregor, Jung, Hans H
Publicado em 2007

Magnetic iron compounds in the human brain: a comparison of tumour and hippocampal tissue

Por Brem, Franziska, Hirt, Ann M, Winklhofer, Michael, Frei, Karl, Yonekawa, Yasuhiro, Wieser, Heinz-Gregor, Dobson, Jon
Publicado em 2006

Characterization of the Gene Expression Profile of Human Hippocampus in Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis

Por Lachos, Julio, Zattoni, Michela, Wieser, Heinz-Gregor, Fritschy, Jean-Marc, Langmann, Thomas, Schmitz, Gerd, Errede, Mariella, Virgintino, Daniela, Yonekawa, Yasuhiro, Frei, Karl
Publicado em 2011

Clinical presentation, epidemiology, neurophysiological findings, treatment and outcome of nonconvulsive status epilepticus: a 3-year prospective, hospital-based study

Por Mesraoua, Boulenouar, Deleu, Dirk, Al Hail, Hassan, Ibrahim, Faisal, Melikyan, Gayane, Al Hussein, Hassan, Singh, Rajvir, Uthman, Basim, Streletz, Leopold, Kaplan, Peter W., Wieser, Heinz Gregor
Publicado no J Drug Assess (2017)

Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study

Por Kasperavičiūtė, Dalia, Catarino, Claudia B., Heinzen, Erin L., Depondt, Chantal, Cavalleri, Gianpiero L., Caboclo, Luis O., Tate, Sarah K., Jamnadas-Khoda, Jenny, Chinthapalli, Krishna, Clayton, Lisa M.S., Shianna, Kevin V., Radtke, Rodney A., Mikati, Mohamad A., Gallentine, William B., Husain, Aatif M., Alhusaini, Saud, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Heuser, Kjell, Amos, Leslie, Ortega, Marcos, Zumsteg, Dominik, Wieser, Heinz-Gregor, Steinhoff, Bernhard J., Krämer, Günter, Hansen, Jörg, Dorn, Thomas, Kantanen, Anne-Mari, Gjerstad, Leif, Peuralinna, Terhi, Hernandez, Dena G., Eriksson, Kai J., Kälviäinen, Reetta K., Doherty, Colin P., Wood, Nicholas W., Pandolfo, Massimo, Duncan, John S., Sander, Josemir W., Delanty, Norman, Goldstein, David B., Sisodiya, Sanjay M.
Publicado em 2010

Rare Deletions at 16p13.11 Predispose to a Diverse Spectrum of Sporadic Epilepsy Syndromes

Por Heinzen, Erin L., Radtke, Rodney A., Urban, Thomas J., Cavalleri, Gianpiero L., Depondt, Chantal, Need, Anna C., Walley, Nicole M., Nicoletti, Paola, Ge, Dongliang, Catarino, Claudia B., Duncan, John S., Kasperavičiūtė, Dalia, Tate, Sarah K., Caboclo, Luis O., Sander, Josemir W., Clayton, Lisa, Linney, Kristen N., Shianna, Kevin V., Gumbs, Curtis E., Smith, Jason, Cronin, Kenneth D., Maia, Jessica M., Doherty, Colin P., Pandolfo, Massimo, Leppert, David, Middleton, Lefkos T., Gibson, Rachel A., Johnson, Michael R., Matthews, Paul M., Hosford, David, Kälviäinen, Reetta, Eriksson, Kai, Kantanen, Anne-Mari, Dorn, Thomas, Hansen, Jörg, Krämer, Günter, Steinhoff, Bernhard J., Wieser, Heinz-Gregor, Zumsteg, Dominik, Ortega, Marcos, Wood, Nicholas W., Huxley-Jones, Julie, Mikati, Mohamad, Gallentine, William B., Husain, Aatif M., Buckley, Patrick G., Stallings, Ray L., Podgoreanu, Mihai V., Delanty, Norman, Sisodiya, Sanjay M., Goldstein, David B.
Publicado em 2010