Absence epilepsy beyond adolescence: an outcome analysis after 45 years of follow-up

Autor: Andrea Kirschbaum, Dieter Janz, Alexander B. Kowski, Bernd J. Vorderwülbecke, Martin Holtkamp

Publikováno v: Journal of Neurology, Neurosurgery & Psychiatry. 89:603-610

ObjectivesDepending on patient age at onset, absence epilepsy is subdivided into childhood and juvenile forms. Absence seizures can occur several times per day (pyknoleptic course) or less frequently than daily (non-pyknoleptic course). Seizures typi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::017dd15112ac4a6d4737fdc79813cdd7
https://doi.org/10.1136/jnnp-2017-317052

Long-term outcome in epilepsy with grand mal on awakening: Forty years of follow-up

Autor: Dieter Janz, Alexander B. Kowski, Hannah Merkle, Martin Holtkamp

Publikováno v: Annals of Neurology. 75:298-302

Epilepsy with grand mal on awakening (EGMA) is a well-defined subtype of idiopathic generalized epilepsy. Patients with follow-up of at least 20 years were assessed retrospectively regarding 5-year terminal seizure remission. Forty-two patients were

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::07c6a50473935f7db859984c9275a996
https://doi.org/10.1002/ana.24103

Die Regatta der härteren Art : Mord am Biggesee

Autor: Dieter Janz

Das geordnete Leben von Iffi gerät gewaltig ins Wanken, als sich aus einem harmlosen Flirt ein Stalking-Fall entwickelt, in den ihr gesamter Freundeskreis hineingezogen wird. Ihr Peiniger legt in kurzer Zeit eine immense kriminelle Energie zutage, M

Ein Forschungsinstitut f�r Epilepsie der Universit�t Bielefeld in Bethel

Autor: Dieter Janz

Publikováno v: Zeitschrift f�r Epileptologie. 16:322-325

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5cac3943f85a4b1208f2f6687301cd96
https://doi.org/10.1007/s10309-003-0022-8

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

Autor: Eva M. Reinthaler, Dennis Lal, Sebastien Lebon, Michael S. Hildebrand, Hans-Henrik M. Dahl, Brigid M. Regan, Martha Feucht, Hannelore Steinböck, Birgit Neophytou, Gabriel M. Ronen, Laurian Roche, Ursula Gruber-Sedlmayr, Julia Geldner, Edda Haberlandt, Per Hoffmann, Stefan Herms, Christian Gieger, Melanie Waldenberger, Andre Franke, Michael Wittig, Susanne Schoch, Albert J. Becker, Andreas Hahn, Katrin Männik, Mohammad R. Toliat, Georg Winterer, Holger Lerche, Peter Nürnberg, Heather Mefford, Ingrid E. Scheffer, Samuel F. Berkovic, Jacques S. Beckmann, Thomas Sander, Sebastien Jacquemont, Alexandre Reymond, Fritz Zimprich, Bernd A. Neubauer, Bernd Neubauer, Martina Mörzinger, Arvid Suls, Sarah Weckhuysen, Lieve Claes, Liesbet Deprez, Katrien Smets, Tine Van Dyck, Tine Deconinck, Peter De Jonghe, Rikke S Møller, Laura L. Klitten, Helle Hjalgrim, Kiel Campus, Ingo Helbig, Hiltrud Muhle, Philipp Ostertag, Sarah von Spiczak, Ulrich Stephani, Holger Trucks, Christian E. Elger, Ailing A. Kleefuß-Lie, Wolfram S. Kunz, Rainer Surges, Verena Gaus, Dieter Janz, Bettina Schmitz, Felix Rosenow, Karl Martin Klein, Philipp S. Reif, Wolfgang H. Oertel, Hajo M. Hamer, Felicitas Becker, Yvonne Weber, Bobby P.C. Koeleman, Carolien de Kovel, Dick Lindhout, Agnès Ameil, Joris Andrieux, Sonia Bouquillon, Odile Boute, Jeanne de Flandre, Jean Marie Cuisset, Jean-Christophe Cuvellier, Roger Salengro, Albert David, Bert de Vries, Marie-Ange Delrue, Martine Doco-Fenzy, Bridget A. Fernandez, Delphine Heron, Boris Keren, Robert Lebel, Bruno Leheup, Suzanne Lewis, Maria Antonietta Mencarelli, Cyril Mignot, Jean-Claude Minet, Alexandre Moerman, Fanny Morice-Picard, Mafalda Mucciolo, Katrin Ounap, Laurent Pasquier, Florence Petit, Francesca Ragona, Evica Rajcan-Separovic, Alessandra Renieri, Claudine Rieubland, Damien Sanlaville, Elisabeth Sarrazin, Yiping Shen, Mieke van Haelst, Anneke Vulto-van Silfhout

Publikováno v: 16p11.2 European Consortium, EPICURE Consortium, The EuroEPINOMICS Consortium & Møller, R S 2014, ' 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy ', Human Molecular Genetics, vol. 23, no. 22, pp. 6069-6080 . https://doi.org/10.1093/hmg/ddu306
Human Molecular Genetics, vol. 23, no. 22, pp. 6069-6080
Human molecular genetics, 23(22), 6069-6080. Oxford University Press
Human molecular genetics
Hum. Mol. Genet. 23, 6069-6080 (2014)
HUMAN MOLECULAR GENETICS
Reinthaler, Eva M; Lal, Dennis; Lebon, Sebastien; Hildebrand, Michael S; Dahl, Hans-Henrik M; Regan, Brigid M; Feucht, Martha; Steinböck, Hannelore; Neophytou, Birgit; Ronen, Gabriel M; Roche, Laurian; Gruber-Sedlmayr, Ursula; Geldner, Julia; Haberlandt, Edda; Hoffmann, Per; Herms, Stefan; Gieger, Christian; Waldenberger, Melanie; Franke, Andre; Wittig, Michael; ... (2014). 16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy. Human molecular genetics, 23(22), pp. 6069-6080. Oxford University Press 10.1093/hmg/ddu306

Rolandic epilepsy (RE) is the most common idiopathic focal childhood epilepsy. Its molecular basis is largely unknown and a complex genetic etiology is assumed in the majority of affected individuals. The present study tested whether six large recurr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::780d31edaa034478bbfc1c48d66221a6
http://hdl.handle.net/11365/975064