Human hippocampus associates information in memory

le Henke, Katharina, Weber, Bruno, Kneifel, Stefan, Wieser, Heinz Gregor, Buck, Alfred
Foilsithe 1999

Selective Alterations in GABA(A) Receptor Subtypes in Human Temporal Lobe Epilepsy

le Loup, Fabienne, Wieser, Heinz-Gregor, Yonekawa, Yasuhiro, Aguzzi, Adriano, Fritschy, Jean-Marc
Foilsithe in J Neurosci (2000)

Non‐convulsive status epilepticus causing focal neurological deficits in CADASIL

le Valko, Philipp O, Siccoli, Massimiliano M, Schiller, Andreas, Wieser, Heinz‐Gregor, Jung, Hans H
Foilsithe 2007

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

le Brem, Franziska, Hirt, Ann M, Winklhofer, Michael, Frei, Karl, Yonekawa, Yasuhiro, Wieser, Heinz-Gregor, Dobson, Jon
Foilsithe 2006

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

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

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

le 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
Foilsithe in J Drug Assess (2017)

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

le 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.
Foilsithe 2010

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

le 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.
Foilsithe 2010