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Items: 1 to 50 of 227

1.

Quality of life and correlating factors in children, adolescents with epilepsy, and their caregivers: A cross-sectional multicenter study from Germany.

Riechmann J, Willems LM, Boor R, Kieslich M, Knake S, Langner C, Neubauer BA, Oberman B, Philippi H, Reese JP, Rochel M, Schubert-Bast S, Seeger J, Seipelt P, Stephani U, Rosenow F, Hamer HM, Strzelczyk A.

Seizure. 2019 Mar 29;69:92-98. doi: 10.1016/j.seizure.2019.03.016. [Epub ahead of print]

PMID:
31004927
2.

Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network.

Lieb W, Jacobs G, Wolf A, Richter G, Gaede KI, Schwarz J, Arnold N, Böhm R, Buyx A, Cascorbi I, Franke A, Glinicke C, Held-Feindt J, Junker R, Kalthoff H, Kramer HH, Leypoldt F, Maass N, Maetzler W, May S, Mehdorn HM, Röcken C, Schafmayer C, Schrappe M, Schreiber S, Sebens S, Stephani U, Synowitz M, Weimer J, Zabel P, Nöthlings U, Röder C, Krawczak M.

J Community Genet. 2019 Mar 29. doi: 10.1007/s12687-019-00417-8. [Epub ahead of print]

PMID:
30927239
3.

Pipeline for Forward Modeling and Source Imaging of Magnetocardiographic Recordings via Spatiotemporal Kalman Filtering.

Habboush N, Hamid L, Siniatchkin M, Stephani U, Galka A.

Conf Proc IEEE Eng Med Biol Soc. 2018 Jul;2018:199-202. doi: 10.1109/EMBC.2018.8512188.

PMID:
30440372
4.

Multifocal epilepsy in children is associated with increased long-distance functional connectivity: An explorative EEG-fMRI study.

Siniatchkin M, Moehring J, Kroeher B, Galka A, von Ondarza G, Moeller F, Wolff S, Tagliazucchi E, Steinmann E, Boor R, Stephani U.

Eur J Paediatr Neurol. 2018 Nov;22(6):1054-1065. doi: 10.1016/j.ejpn.2018.07.001. Epub 2018 Jul 5.

PMID:
30017619
5.

Variants in the ATP1A3 Gene Mutations within Severe Apnea Starting in Early Infancy: An Observational Study of Two Cases with a Possible Relation to Epileptic Activity.

Holze N, Baalen AV, Stephani U, Helbig I, Muhle H.

Neuropediatrics. 2018 Oct;49(5):342-346. doi: 10.1055/s-0038-1653978. Epub 2018 May 25.

PMID:
29801192
6.

Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood.

Vögtle FN, Brändl B, Larson A, Pendziwiat M, Friederich MW, White SM, Basinger A, Kücükköse C, Muhle H, Jähn JA, Keminer O, Helbig KL, Delto CF, Myketin L, Mossmann D, Burger N, Miyake N, Burnett A, van Baalen A, Lovell MA, Matsumoto N, Walsh M, Yu HC, Shinde DN, Stephani U, Van Hove JLK, Müller FJ, Helbig I.

Am J Hum Genet. 2018 Apr 5;102(4):557-573. doi: 10.1016/j.ajhg.2018.02.014. Epub 2018 Mar 22.

7.

Effects of Levetiracetam and Sulthiame on EEG in benign epilepsy with centrotemporal spikes: A randomized controlled trial.

Tacke M, Borggraefe I, Gerstl L, Heinen F, Vill K, Bonfert M, Bast T; HEAD Study group, Neubauer BA, Baumeister F, Baethmann M, Bentele K, Blank C, Blank HM, Bode H, Bosch F, Brandl U, Brockmann K, Dahlem P, Ernst JP, Feldmann E, Fiedler A, Gerigk M, Heß S, Hikel C, Hoffmann HG, Kieslich M, Klepper J, Kluger G, Koch H, Koch W, Korinthenberg R, Krois I, Kühne H, Kurlemann G, Mandl M, Mause U, Navratil P, Opp J, Penzien J, Prietsch V, Quattländer A, Rating D, Schara U, Shamdeen MG, Sprinz A, Wendker-Magrabi H, Stephani U, Muhle H, Straßburg HM, Töpke B, Trollmann R, Tuschen-Hofstätter E, Waltz S, Weber G, Wien FU, Wolff M, Polster T, Freitag H, Sönmez Ö, Reinhardt K, Traus M, Hoovey Z.

Seizure. 2018 Mar;56:115-120. doi: 10.1016/j.seizure.2018.01.015. Epub 2018 Feb 3.

8.

Source reconstruction via the spatiotemporal Kalman filter and LORETA from EEG time series with 32 or fewer electrodes.

Hamid L, Al Farawn A, Merlet I, Japaridze N, Heute U, Stephani U, Galka A, Wendling F, Siniatchkin M.

Conf Proc IEEE Eng Med Biol Soc. 2017 Jul;2017:2218-2222. doi: 10.1109/EMBC.2017.8037295.

PMID:
29060337
9.

Spatial projection as a preprocessing step for EEG source reconstruction using spatiotemporal Kalman filtering.

Hamid L, Al Farawn A, Merlet I, Japaridze N, Heute U, Stephani U, Galka A, Wendling F, Siniatchkin M.

Conf Proc IEEE Eng Med Biol Soc. 2017 Jul;2017:2213-2217. doi: 10.1109/EMBC.2017.8037294.

PMID:
29060336
10.

In response: Neuronal networks in epileptic encephalopathies with CSWS.

Japaridze N, Muthuraman M, Dierck C, von Spiczak S, Stephani U, Siniatchkin M.

Epilepsia. 2017 Jul;58(7):1297-1298. doi: 10.1111/epi.13788. No abstract available.

11.

DNM1 encephalopathy: A new disease of vesicle fission.

von Spiczak S, Helbig KL, Shinde DN, Huether R, Pendziwiat M, Lourenço C, Nunes ME, Sarco DP, Kaplan RA, Dlugos DJ, Kirsch H, Slavotinek A, Cilio MR, Cervenka MC, Cohen JS, McClellan R, Fatemi A, Yuen A, Sagawa Y, Littlejohn R, McLean SD, Hernandez-Hernandez L, Maher B, Møller RS, Palmer E, Lawson JA, Campbell CA, Joshi CN, Kolbe DL, Hollingsworth G, Neubauer BA, Muhle H, Stephani U, Scheffer IE, Pena SDJ, Sisodiya SM, Helbig I; Epi4K Consortium; EuroEPINOMICS-RES NLES Working Group.

Neurology. 2017 Jul 25;89(4):385-394. doi: 10.1212/WNL.0000000000004152. Epub 2017 Jun 30.

12.

Gene expression analysis in untreated absence epilepsy demonstrates an inconsistent pattern.

von Deimling M, Häsler R, Steinbach V, Holterhus PM, von Spiczak S, Stephani U, Helbig I, Muhle H.

Epilepsy Res. 2017 May;132:84-90. doi: 10.1016/j.eplepsyres.2017.02.008. Epub 2017 Feb 28.

PMID:
28324682
13.

Smad anchor for receptor activation contributes to seizures in temporal lobe epilepsy.

Yu W, Du Y, Zou Y, Wang X, Stephani U, Lü Y.

Synapse. 2017 Mar;71(3). doi: 10.1002/syn.21957. Epub 2017 Jan 13.

PMID:
28035691
14.

Pitfalls in genetic testing: the story of missed SCN1A mutations.

Djémié T, Weckhuysen S, von Spiczak S, Carvill GL, Jaehn J, Anttonen AK, Brilstra E, Caglayan HS, de Kovel CG, Depienne C, Gaily E, Gennaro E, Giraldez BG, Gormley P, Guerrero-López R, Guerrini R, Hämäläinen E, Hartmann C, Hernandez-Hernandez L, Hjalgrim H, Koeleman BP, Leguern E, Lehesjoki AE, Lemke JR, Leu C, Marini C, McMahon JM, Mei D, Møller RS, Muhle H, Myers CT, Nava C, Serratosa JM, Sisodiya SM, Stephani U, Striano P, van Kempen MJ, Verbeek NE, Usluer S, Zara F, Palotie A, Mefford HC, Scheffer IE, De Jonghe P, Helbig I, Suls A; EuroEPINOMICS‐RES Dravet working group.

Mol Genet Genomic Med. 2016 Apr 14;4(4):457-64. doi: 10.1002/mgg3.217. eCollection 2016 Jul.

15.

Neuronal networks in epileptic encephalopathies with CSWS.

Japaridze N, Muthuraman M, Dierck C, von Spiczak S, Boor R, Mideksa KG, Anwar RA, Deuschl G, Stephani U, Siniatchkin M.

Epilepsia. 2016 Aug;57(8):1245-55. doi: 10.1111/epi.13428. Epub 2016 Jun 15.

16.

Intravenous lacosamide in clinical practice-Results from an independent registry.

Lang N, Lange M, Schmitt FC, Bös M, Weber Y, Evers S, Burghaus L, Kellinghaus C, Schubert-Bast S, Bösel J, Lammers T, Sabolek M, van Baalen A, Dziewas R, Kraft A, Ruf S, Stephani U.

Seizure. 2016 Jul;39:5-9. doi: 10.1016/j.seizure.2016.01.008. Epub 2016 Jan 12.

17.

Analysis of epileptic seizure count time series by ensemble state space modelling.

Galka A, Boor R, Doege C, von Spiczak S, Stephani U, Siniatchkin M.

Conf Proc IEEE Eng Med Biol Soc. 2015 Aug;2015:5601-5. doi: 10.1109/EMBC.2015.7319662.

PMID:
26737562
18.

The choice of the source space and the Laplacian matrix in LORETA and the spatio-temporal Kalman filter EEG inverse methods.

Habboush N, Hamid L, Japaridze N, Wiegand G, Heute U, Stephani U, Galka A, Siniatchkin M.

Conf Proc IEEE Eng Med Biol Soc. 2015 Aug;2015:2745-9. doi: 10.1109/EMBC.2015.7318960.

PMID:
26736860
19.

The performance of the spatiotemporal Kalman filter and LORETA in seizure onset localization.

Hamid L, Sarabi M, Japaridze N, Wiegand G, Heute U, Stephani U, Galka A, Siniatchkin M.

Conf Proc IEEE Eng Med Biol Soc. 2015 Aug;2015:2741-4. doi: 10.1109/EMBC.2015.7318959.

PMID:
26736859
20.

The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.

Larsen J, Johannesen KM, Ek J, Tang S, Marini C, Blichfeldt S, Kibaek M, von Spiczak S, Weckhuysen S, Frangu M, Neubauer BA, Uldall P, Striano P, Zara F; MAE working group of EuroEPINOMICS RES Consortium, Kleiss R, Simpson M, Muhle H, Nikanorova M, Jepsen B, Tommerup N, Stephani U, Guerrini R, Duno M, Hjalgrim H, Pal D, Helbig I, Møller RS.

Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.

21.

EEG-MEG Integration Enhances the Characterization of Functional and Effective Connectivity in the Resting State Network.

Muthuraman M, Moliadze V, Mideksa KG, Anwar AR, Stephani U, Deuschl G, Freitag CM, Siniatchkin M.

PLoS One. 2015 Oct 28;10(10):e0140832. doi: 10.1371/journal.pone.0140832. eCollection 2015.

22.

Costs of epilepsy and cost-driving factors in children, adolescents, and their caregivers in Germany.

Riechmann J, Strzelczyk A, Reese JP, Boor R, Stephani U, Langner C, Neubauer BA, Oberman B, Philippi H, Rochel M, Seeger J, Seipelt P, Oertel WH, Dodel R, Rosenow F, Hamer HM; EpiPaed Study Group.

Epilepsia. 2015 Sep;56(9):1388-97. doi: 10.1111/epi.13089. Epub 2015 Aug 3.

23.

Investigation of GRIN2A in common epilepsy phenotypes.

Lal D, Steinbrücker S, Schubert J, Sander T, Becker F, Weber Y, Lerche H, Thiele H, Krause R, Lehesjoki AE, Nürnberg P, Palotie A, Neubauer BA, Muhle H, Stephani U, Helbig I, Becker AJ, Schoch S, Hansen J, Dorn T, Hohl C, Lüscher N; Epicure consortium; EuroEPINOMICS-CoGIE consortium, von Spiczak S, Lemke JR.

Epilepsy Res. 2015 Sep;115:95-9. doi: 10.1016/j.eplepsyres.2015.05.010. Epub 2015 Jun 2.

PMID:
26220384
24.

Intravenous levetiracetam in clinical practice--Results from an independent registry.

Lang N, Esser W, Evers S, Kellinghaus C, Nguento A, Schlegel U, Gaida B, Gburek-Augustat J, Altenmüller DM, Burghaus L, Hoffmann F, Fiedler B, Bast T, Rehfeld T, Happe S, Seitz RJ, Boor R, Stephani U.

Seizure. 2015 Jul;29:109-13. doi: 10.1016/j.seizure.2015.03.018. Epub 2015 Apr 13.

25.

Array-based DNA methylation analysis in individuals with developmental delay/intellectual disability and normal molecular karyotype.

Kolarova J, Tangen I, Bens S, Gillessen-Kaesbach G, Gutwein J, Kautza M, Rydzanicz M, Stephani U, Siebert R, Ammerpohl O, Caliebe A.

Eur J Med Genet. 2015 Aug;58(8):419-25. doi: 10.1016/j.ejmg.2015.05.001. Epub 2015 May 21.

PMID:
26003415
26.

Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies.

Lal D, Ruppert AK, Trucks H, Schulz H, de Kovel CG, Kasteleijn-Nolst Trenité D, Sonsma AC, Koeleman BP, Lindhout D, Weber YG, Lerche H, Kapser C, Schankin CJ, Kunz WS, Surges R, Elger CE, Gaus V, Schmitz B, Helbig I, Muhle H, Stephani U, Klein KM, Rosenow F, Neubauer BA, Reinthaler EM, Zimprich F, Feucht M, Møller RS, Hjalgrim H, De Jonghe P, Suls A, Lieb W, Franke A, Strauch K, Gieger C, Schurmann C, Schminke U, Nürnberg P; EPICURE Consortium, Sander T.

PLoS Genet. 2015 May 7;11(5):e1005226. doi: 10.1371/journal.pgen.1005226. eCollection 2015 May.

27.

Neuronal Networks during Burst Suppression as Revealed by Source Analysis.

Japaridze N, Muthuraman M, Reinicke C, Moeller F, Anwar AR, Mideksa KG, Pressler R, Deuschl G, Stephani U, Siniatchkin M.

PLoS One. 2015 Apr 30;10(4):e0123807. doi: 10.1371/journal.pone.0123807. eCollection 2015.

28.

CHD2 variants are a risk factor for photosensitivity in epilepsy.

Galizia EC, Myers CT, Leu C, de Kovel CG, Afrikanova T, Cordero-Maldonado ML, Martins TG, Jacmin M, Drury S, Krishna Chinthapalli V, Muhle H, Pendziwiat M, Sander T, Ruppert AK, Møller RS, Thiele H, Krause R, Schubert J, Lehesjoki AE, Nürnberg P, Lerche H; EuroEPINOMICS CoGIE Consortium, Palotie A, Coppola A, Striano S, Gaudio LD, Boustred C, Schneider AL, Lench N, Jocic-Jakubi B, Covanis A, Capovilla G, Veggiotti P, Piccioli M, Parisi P, Cantonetti L, Sadleir LG, Mullen SA, Berkovic SF, Stephani U, Helbig I, Crawford AD, Esguerra CV, Kasteleijn-Nolst Trenité DG, Koeleman BP, Mefford HC, Scheffer IE, Sisodiya SM.

Brain. 2015 May;138(Pt 5):1198-207. doi: 10.1093/brain/awv052. Epub 2015 Mar 17.

29.

Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiences.

Biró A, Stephani U, Tarallo T, Bast T, Schlachter K, Fleger M, Kurlemann G, Fiedler B, Leiz S, Nikanorova M, Wolff M, Müller A, Selch C, Staudt M, Kluger G.

Neuropediatrics. 2015 Apr;46(2):110-6. doi: 10.1055/s-0035-1546276. Epub 2015 Mar 2.

PMID:
25730374
30.

Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis.

Hartmann C, von Spiczak S, Suls A, Weckhuysen S, Buyse G, Vilain C, Van Bogaert P, De Jonghe P, Cook J, Muhle H, Stephani U, Helbig I, Mefford HC.

Epilepsia. 2015 Mar;56(3):e26-32. doi: 10.1111/epi.12920. Epub 2015 Feb 17.

31.

Validating the effect of muscle artifact suppression in localizing focal epilepsy.

Mideksa KG, Santillan-Guzman A, Japaridze N, Galka A, Stephani U, Deuschl G, Heute U, Muthuraman M.

Conf Proc IEEE Eng Med Biol Soc. 2014;2014:3841-4. doi: 10.1109/EMBC.2014.6944461.

PMID:
25570829
32.

A computational study of stimulus driven epileptic seizure abatement.

Taylor PN, Wang Y, Goodfellow M, Dauwels J, Moeller F, Stephani U, Baier G.

PLoS One. 2014 Dec 22;9(12):e114316. doi: 10.1371/journal.pone.0114316. eCollection 2014.

33.

Long-term seizure outcome in 211 patients with focal cortical dysplasia.

Fauser S, Essang C, Altenmüller DM, Staack AM, Steinhoff BJ, Strobl K, Bast T, Schubert-Bast S, Stephani U, Wiegand G, Prinz M, Brandt A, Zentner J, Schulze-Bonhage A.

Epilepsia. 2015 Jan;56(1):66-76. doi: 10.1111/epi.12876. Epub 2014 Dec 13.

34.

Altered information processing in children with focal epilepsies with and without intellectual disability.

Japaridze N, Schark M, von-Ondarza G, Boor R, Muhle H, Gerber WD, Stephani U, Siniatchkin M.

Funct Neurol. 2014 Apr-Jun;29(2):87-97.

35.
36.

Evaluation of health-care utilization in patients with Dravet syndrome and on adjunctive treatment with stiripentol and clobazam.

Strzelczyk A, Schubert-Bast S, Reese JP, Rosenow F, Stephani U, Boor R.

Epilepsy Behav. 2014 May;34:86-91. doi: 10.1016/j.yebeh.2014.03.014. Epub 2014 Apr 13.

PMID:
24727467
37.

EEG-fMRI in myoclonic astatic epilepsy (Doose syndrome).

Moeller F, Groening K, Moehring J, Muhle H, Wolff S, Jansen O, Stephani U, Siniatchkin M.

Neurology. 2014 Apr 29;82(17):1508-13. doi: 10.1212/WNL.0000000000000359. Epub 2014 Apr 2.

PMID:
24696509
38.

Risk factors of cognitive outcome in patients with atypical benign partial epilepsy/pseudo-Lennox syndrome (ABPE/PLS) and continues spike and wave during sleep (CSWS).

Japaridze N, Menzel E, von Ondarza G, Steinmann E, Stephani U.

Eur J Paediatr Neurol. 2014 May;18(3):368-75. doi: 10.1016/j.ejpn.2014.01.012. Epub 2014 Feb 15.

PMID:
24594429
39.

Cortical Thickness Changes Associated with Photoparoxysmal Response.

Hanganu A, Groppa SA, Deuschl G, Siebner H, Moeller F, Siniatchkin M, Stephani U, Groppa S.

Brain Topogr. 2015 Sep;28(5):702-709. doi: 10.1007/s10548-014-0353-y. Epub 2014 Feb 1.

PMID:
24487625
40.

Phenotypic spectrum of eleven patients and five novel MTFMT mutations identified by exome sequencing and candidate gene screening.

Haack TB, Gorza M, Danhauser K, Mayr JA, Haberberger B, Wieland T, Kremer L, Strecker V, Graf E, Memari Y, Ahting U, Kopajtich R, Wortmann SB, Rodenburg RJ, Kotzaeridou U, Hoffmann GF, Sperl W, Wittig I, Wilichowski E, Schottmann G, Schuelke M, Plecko B, Stephani U, Strom TM, Meitinger T, Prokisch H, Freisinger P.

Mol Genet Metab. 2014 Mar;111(3):342-352. doi: 10.1016/j.ymgme.2013.12.010. Epub 2013 Dec 25.

PMID:
24461907
41.

Developmental changes of neuronal networks associated with strategic social decision-making.

Steinmann E, Schmalor A, Prehn-Kristensen A, Wolff S, Galka A, Möhring J, Gerber WD, Petermann F, Stephani U, Siniatchkin M.

Neuropsychologia. 2014 Apr;56:37-46. doi: 10.1016/j.neuropsychologia.2013.12.025. Epub 2014 Jan 9.

PMID:
24412687
42.

Structural genomic variation in childhood epilepsies with complex phenotypes.

Helbig I, Swinkels ME, Aten E, Caliebe A, van 't Slot R, Boor R, von Spiczak S, Muhle H, Jähn JA, van Binsbergen E, van Nieuwenhuizen O, Jansen FE, Braun KP, de Haan GJ, Tommerup N, Stephani U, Hjalgrim H, Poot M, Lindhout D, Brilstra EH, Møller RS, Koeleman BP.

Eur J Hum Genet. 2014 Jul;22(7):896-901. doi: 10.1038/ejhg.2013.262. Epub 2013 Nov 27.

43.

Iterative phenotyping of 15q11.2, 15q13.3 and 16p13.11 microdeletion carriers in pediatric epilepsies.

Jähn JA, von Spiczak S, Muhle H, Obermeier T, Franke A, Mefford HC, Stephani U, Helbig I.

Epilepsy Res. 2014 Jan;108(1):109-16. doi: 10.1016/j.eplepsyres.2013.10.001. Epub 2013 Oct 26.

PMID:
24246141
44.

Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures.

Elshoff L, Muthuraman M, Anwar AR, Deuschl G, Stephani U, Raethjen J, Siniatchkin M.

PLoS One. 2013 Oct 23;8(10):e78422. doi: 10.1371/journal.pone.0078422. eCollection 2013.

45.

Atypical vitamin B6 deficiency: a rare cause of unexplained neonatal and infantile epilepsies.

Baumgart A, Spiczak Sv, Verhoeven-Duif NM, Møller RS, Boor R, Muhle H, Jähn JA, Klitten LL, Hjalgrim H, Lindhout D, Stephani U, van Kempen MJ, Helbig I.

J Child Neurol. 2014 May;29(5):704-7. doi: 10.1177/0883073813505354. Epub 2013 Oct 10.

PMID:
24114605
46.

MEG-EEG fusion by Kalman filtering within a source analysis framework.

Hamid L, Aydin Ü, Wolters C, Stephani U, Siniatchkin M, Galka A.

Conf Proc IEEE Eng Med Biol Soc. 2013;2013:4819-22. doi: 10.1109/EMBC.2013.6610626.

PMID:
24110813
47.

DBS artifact suppression using a time-frequency domain filter.

Santillán-Guzmán A, Heute U, Muthuraman M, Stephani U, Galka A.

Conf Proc IEEE Eng Med Biol Soc. 2013;2013:4815-8. doi: 10.1109/EMBC.2013.6610625.

PMID:
24110812
48.

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes.

Lemke JR, Lal D, Reinthaler EM, Steiner I, Nothnagel M, Alber M, Geider K, Laube B, Schwake M, Finsterwalder K, Franke A, Schilhabel M, Jähn JA, Muhle H, Boor R, Van Paesschen W, Caraballo R, Fejerman N, Weckhuysen S, De Jonghe P, Larsen J, Møller RS, Hjalgrim H, Addis L, Tang S, Hughes E, Pal DK, Veri K, Vaher U, Talvik T, Dimova P, Guerrero López R, Serratosa JM, Linnankivi T, Lehesjoki AE, Ruf S, Wolff M, Buerki S, Wohlrab G, Kroell J, Datta AN, Fiedler B, Kurlemann G, Kluger G, Hahn A, Haberlandt DE, Kutzer C, Sperner J, Becker F, Weber YG, Feucht M, Steinböck H, Neophythou B, Ronen GM, Gruber-Sedlmayr U, Geldner J, Harvey RJ, Hoffmann P, Herms S, Altmüller J, Toliat MR, Thiele H, Nürnberg P, Wilhelm C, Stephani U, Helbig I, Lerche H, Zimprich F, Neubauer BA, Biskup S, von Spiczak S.

Nat Genet. 2013 Sep;45(9):1067-72. doi: 10.1038/ng.2728. Epub 2013 Aug 11.

PMID:
23933819
49.

Everolimus in tuberous sclerosis patients with intractable epilepsy: a treatment option?

Wiegand G, May TW, Ostertag P, Boor R, Stephani U, Franz DN.

Eur J Paediatr Neurol. 2013 Nov;17(6):631-8. doi: 10.1016/j.ejpn.2013.06.002. Epub 2013 Jul 8.

PMID:
23845174
50.

Reoperation for refractory epilepsy in childhood: a second chance for selected patients.

Ramantani G, Strobl K, Stathi A, Brandt A, Schubert-Bast S, Wiegand G, Korinthenberg R, Stephani U, van Velthoven V, Zentner J, Schulze-Bonhage A, Bast T.

Neurosurgery. 2013 Oct;73(4):695-704; discussion 704. doi: 10.1227/NEU.0000000000000081.

PMID:
23842559

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