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Felix Rosenow
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Presurgical evaluation of epilepsy
F Rosenow, H Lüders
Brain 124 (9), 1683-1700, 2001
21222001
Semiological seizure classification.
H Lüders, J Acharya, C Baumgartner, S Benbadis, A Bleasel, R Burgess, ...
Epilepsia 39 (9), 1006-1013, 1998
9301998
Histopathological findings in brain tissue obtained during epilepsy surgery
I Blumcke, R Spreafico, G Haaker, R Coras, K Kobow, CG Bien, M Pfäfflin, ...
New England Journal of Medicine 377 (17), 1648-1656, 2017
8762017
15q13. 3 microdeletions increase risk of idiopathic generalized epilepsy
I Helbig, HC Mefford, AJ Sharp, M Guipponi, M Fichera, A Franke, ...
Nature genetics 41 (2), 160-162, 2009
6922009
Incidence of status epilepticus in adults in Germany: a prospective, population‐based study
S Knake, F Rosenow, M Vescovi, WH Oertel, HH Mueller, A Wirbatz, ...
Epilepsia 42 (6), 714-718, 2001
6382001
Leitlinien für Diagnostik und Therapie in der Neurologie
HC Diener, C Weimar, P Berlit, G Deuschl, C Elger, R Gold, W Hacke, ...
Thieme Verlag, 2012
5372012
Recurrent microdeletions at 15q11. 2 and 16p13. 11 predispose to idiopathic generalized epilepsies
CGF de Kovel, H Trucks, I Helbig, HC Mefford, C Baker, C Leu, C Kluck, ...
Brain 133 (1), 23-32, 2010
5182010
Randomized phase III study 306: adjunctive perampanel for refractory partial-onset seizures
GL Krauss, JM Serratosa, V Villanueva, M Endziniene, Z Hong, J French, ...
Neurology 78 (18), 1408-1415, 2012
5012012
State of the art: pharmacologic effects on cortical excitability measures tested by transcranial magnetic stimulation
W Paulus, J Classen, LG Cohen, CH Large, V Di Lazzaro, M Nitsche, ...
Brain stimulation 1 (3), 151-163, 2008
4732008
De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies
S Appenzeller, R Balling, N Barisic, S Baulac, H Caglayan, D Craiu, ...
The American Journal of Human Genetics 95 (4), 360-370, 2014
4682014
Proposed consensus definitions for new‐onset refractory status epilepticus (NORSE), febrile infection‐related epilepsy syndrome (FIRES), and related conditions
LJ Hirsch, N Gaspard, A van Baalen, R Nabbout, S Demeret, ...
Epilepsia 59 (4), 739-744, 2018
4542018
Adjunctive lacosamide for partial‐onset seizures: efficacy and safety results from a randomized controlled trial
P Halász, R Kälviäinen, M Mazurkiewicz‐Beldzińska, F Rosenow, P Doty, ...
Epilepsia 50 (3), 443-453, 2009
4422009
Cytokines and epilepsy
G Li, S Bauer, M Nowak, B Norwood, B Tackenberg, F Rosenow, S Knake, ...
Seizure 20 (3), 249-256, 2011
3482011
The phenotypic spectrum of SCN8A encephalopathy
J Larsen, GL Carvill, E Gardella, G Kluger, G Schmiedel, N Barisic, ...
Neurology 84 (5), 480-489, 2015
3072015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy
S Syrbe, UBS Hedrich, E Riesch, T Djémié, S Müller, RS Møller, B Maher, ...
Nature genetics 47 (4), 393-399, 2015
3032015
Transcutaneous vagus nerve stimulation (tVNS) for treatment of drug-resistant epilepsy: a randomized, double-blind clinical trial (cMPsE02)
S Bauer, H Baier, C Baumgartner, K Bohlmann, S Fauser, W Graf, ...
Brain stimulation 9 (3), 356-363, 2016
2902016
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
2702019
Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study
HJ Lamberink, WM Otte, I Blümcke, KPJ Braun, M Aichholzer, I Amorim, ...
The Lancet Neurology 19 (9), 748-757, 2020
2682020
International consensus based review and recommendations for minimum reporting standards in research on transcutaneous vagus nerve stimulation (version 2020)
AD Farmer, A Strzelczyk, A Finisguerra, AV Gourine, A Gharabaghi, ...
Frontiers in human neuroscience 14, 568051, 2021
2662021
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
A Suls, JA Jaehn, A Kecskés, Y Weber, S Weckhuysen, DC Craiu, ...
The American Journal of Human Genetics 93 (5), 967-975, 2013
2642013
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