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Forschungsdatenbank PMU-SQQUID

UNIVERSITÄTSINSTITUT FÜR REHABILITATION, TRANSITION UND PALLIATION VON NEUROLOGISCH KRANKEN KINDERN:

PUBLIKATIONEN | Mitarbeiter/innen

123 Publikationen

2022

Beiträge in Fachzeitschriften

PIGN encephalopathy: Characterizing the epileptology.
Bayat, A; de Valles-Ibáñez, G; Pendziwiat, M; Knaus, A; Alt, K; Biamino, E; Bley, A; Calvert, S; Carney, P; Caro-Llopis, A; Ceulemans, B; Cousin, J; Davis, S; des Portes, V; Edery, P; England, E; Ferreira, C; Freeman, J; Gener, B; Gorce, M; Heron, D; Hildebrand, MS; Jezela-Stanek, A; Jouk, PS; Keren, B; Kloth, K; Kluger, G; Kuhn, M; Lemke, JR; Li, H; Martinez, F; Maxton, C; Mefford, HC; Merla, G; Mierzewska, H; Muir, A; Monfort, S; Nicolai, J; Norman, J; O"Grady, G; Oleksy, B; Orellana, C; Orec, LE; Peinhardt, C; Pronicka, E; Rosello, M; Santos-Simarro, F; Schwaibold, EMC; Stegmann, APA; Stumpel, CT; Szczepanik, E; Terczyńska, I; Thevenon, J; Tzschach, A; Van Bogaert, P; Vittorini, R; Walsh, S; Weckhuysen, S; Weissman, B; Wolfe, L; Reymond, A; De Nittis, P; Poduri, A; Olson, H; Striano, P; Lesca, G; Scheffer, IE; Møller, RS; Sadleir, LG;
Epilepsia. 2022; 63(4): 974-991.
Originalarbeiten (Zeitschrift)
Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences.
Cerulli Irelli, E; Cocchi, E; Ramantani, G; Caraballo, RH; Giuliano, L; Yilmaz, T; Morano, A; Panagiotakaki, E; Operto, FF; Gonzalez Giraldez, B; Silvennoinen, K; Casciato, S; Comajuan, M; Balestrini, S; Fortunato, F; Coppola, A; Di Gennaro, G; Labate, A; Sofia, V; Kluger, GJ; Kasteleijn-Nolst Trenité, DGA; Gambardella, A; Baykan, B; Sisodiya, SM; Arzimanoglou, A; Striano, P; Di Bonaventura, C;
Neurology. 2022; 98(18): e1865-e1876.
Originalarbeiten (Zeitschrift)
The spectrum of epilepsy with eyelid myoclonia: delineation of disease subtypes from a large multicenter study.
Cerulli Irelli, E; Cocchi, E; Ramantani, G; Riva, A; Caraballo, RH; Morano, A; Giuliano, L; Yilmaz, T; Panagiotakaki, E; Operto, FF; Giraldez, BG; Balestrini, S; Silvennoinen, K; Casciato, S; Comajuan, M; Fortunato, F; Giallonardo, AT; Gamirova, R; Coppola, A; Di Gennaro, G; Labate, A; Sofia, V; Kluger, GJ; Gambardella, A; Kasteleijn-Nolst Trenite, D; Baykan, B; Sisodiya, SM; Arzimanoglou, A; Striano, P; Di Bonaventura, C;
Epilepsia. 2022;
Originalarbeiten (Zeitschrift)
Efficacy, Tolerability, and Retention of Antiseizure Medications in PRRT2-Associated Infantile Epilepsy
Doring, JH; Saffari, A; Bast, T; Brockmann, K; Ehrhardt, L; Fazeli, W; Janzarik, WG; Klabunde-Cherwon, A; Kluger, G; Muhle, H; Pendziwiat, M; Moller, RS; Platzer, K; Santos, JL; Schroter, J; Hoffmann, GF; Kolker, S; Syrbe, S
NEUROL-GENET. 2022; 8(5): e200020
Originalarbeiten (Zeitschrift)
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real-world practice setting: A report from the Fenfluramine European Early Access Program
Guerrini, R; Specchio, N; Aledo-Serrano, A; Pringsheim, M; Darra, F; Mayer, T; Gil-Nagel, A; Polster, T; Zuberi, SM; Lothe, A; Gammaitoni, A; Strzelczyk, A
EPILEPSIA OPEN. 2022;
Originalarbeiten (Zeitschrift)
[Hemispherotomy in pediatric epilepsy surgery-Surgical, epileptological and functional aspects].
Hartlieb, T; Kudernatsch, M; Staudt, M
Nervenarzt. 2022; 93(2):142-150
Übersichtsarbeiten
Multilobar unilateral hypoplasia with emphasis on the posterior quadrant and severe epilepsy in children with FCD ILAE Type 1A.
Holthausen, H; Coras, R; Tang, YY; Bai, L; Wang, RN; Pieper, T; Kudernatsch, M; Hartlieb, T; Staudt, M; Winkler, P; Hofer, W; Jabari, S; Kobow, K; Blumcke, I
Epilepsia. 2022; 63(1):42-60
Originalarbeiten (Zeitschrift)
Surgery for frontal lobe epilepsy: lobectomy or disconnective procedure?
Kudernatsch, M; Pieper, T; Hartlieb, T
Z EPILEPTOL. 2022;
Originalarbeiten (Zeitschrift)
"Weak with Laughter"-Cataplexy as a Hint for Early Diagnosis of Niemann-Pick Type C?
Leppmeier, V; Veit, S; Demund, S; Makowski, C; Kluger, G;
Neuropediatrics. 2022; 53(2):146
Fallberichte
Targeted Molecular Strategies for Genetic Neurodevelopmental Disorders: Emerging Lessons from Dravet Syndrome.
Lersch, R; Jannadi, R; Grosse, L; Wagner, M; Schneider, MF; von Stulpnagel, C; Heinen, F; Potschka, H; Borggraefe, I
NEUROSCIENTIST. 2022; 10738584221088244
Übersichtsarbeiten
Biallelic variants in PIGN cause Fryns syndrome, multiple congenital anomalies-hypotonia-seizures syndrome, and neurologic phenotypes: A genotype-phenotype correlation study.
Loong, L; Tardivo, A; Knaus, A; Hashim, M; Pagnamenta, AT; Alt, K; Böhrer-Rabel, H; Caro-Llopis, A; Cole, T; Distelmaier, F; Edery, P; Ferreira, CR; Jezela-Stanek, A; Kerr, B; Kluger, G; Krawitz, PM; Kuhn, M; Lemke, JR; Lesca, G; Lynch, SA; Martinez, F; Maxton, C; Mierzewska, H; Monfort, S; Nicolai, J; Orellana, C; Pal, DK; Płoski, R; Quarrell, OW; Rosello, M; Rydzanicz, M; Sabir, A; Śmigiel, R; Stegmann, APA; Stewart, H; Stumpel, C; Szczepanik, E; Tzschach, A; Wolfe, L; Taylor, JC; Murakami, Y; Kinoshita, T; Bayat, A; Kini, U;
Genet Med. 2022;
Originalarbeiten (Zeitschrift)
KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism
Miceli, F; Millevert, C; Soldovieri, MV; Mosca, I; Ambrosino, P; Carotenuto, L; Schrader, D; Lee, HK; Riviello, J; Hong, W; Risen, S; Emrick, L; Amin, H; Ville, D; Edery, P; de Bellescize, J; Michaud, V; Van-Gils, J; Goizet, C; Willemsen, MH; Kleefstra, T; Moller, RS; Bayat, A; Devinsky, O; Sands, T; Korenke, GC; Kluger, G; Mefford, HC; Brilstra, E; Lesca, G; Milh, M; Cooper, EC; Taglialatela, M; Weckhuysen, S
EBIOMEDICINE. 2022; 81: 104130
Originalarbeiten (Zeitschrift)
New-onset refractory status epilepticus (NORSE) and febrile infection-related epilepsy syndrome (FIRES) of unknown aetiology: A comparison of the incomparable?
Nausch, E; Schaffeldt, L; Tautorat, I; Margraf, NG; Häusler, M; Kluger, G; Kellinghaus, C; Borzikowsky, C; Laufs, H; van Baalen, A;
Seizure. 2022; 96:18-21
Originalarbeiten (Zeitschrift)
Efficacy and mid-term outcome of middle meningeal artery embolization with or without burr hole evacuation for chronic subdural hematoma compared with burr hole evacuation alone
Onyinzo, C; Berlis, A; Abel, M; Kudernatsch, M; Maurer, CJ
J NEUROINTERV SURG. 2022;
Originalarbeiten (Zeitschrift)
Clinical and epilepsy characteristics in Wolf-Hirschhorn syndrome (4p-): A review.
Paprocka, J; Kaminiów, K; Yetkin, O; Tekturk, P; Baykan, B; Leiz, S; Kluger, G; Striano, P;
Seizure. 2022;
Übersichtsarbeiten
Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome.
Strzelczyk, A; Kurlemann, G; Bast, T; Bettendorf, U; Kluger, G; Mayer, T; Neubauer, BA; Polster, T; von Spiczak, S; Trollmann, R; Wolff, M; Toward, T; Gruenert, J; Gibson, E; Pritchard, C; Carroll, J; Rosenow, F; Schubert-Bast, S;
Neurol Res Pract. 2022; 4(1): 22
Originalarbeiten (Zeitschrift)

2021

Beiträge in Fachzeitschriften

Deep Brain Stimulation in KMT2B-Related Dystonia: Case Report and Review of the Literature With Special Emphasis on Dysarthria and Speech.
Abel, M; Pfister, R; Hussein, I; Alsalloum, F; Onyinzo, C; Kappl, S; Zech, M; Demmel, W; Staudt, M; Kudernatsch, M; Berweck, S
FRONT NEUROL. 2021; 12: 662910
Übersichtsarbeiten
Clinical and Genetic Features in Patients With Reflex Bathing Epilepsy.
Accogli, A; Wiegand, G; Scala, M; Cerminara, C; Iacomino, M; Riva, A; Carlini, B; Camerota, L; Belcastro, V; Prontera, P; Fernandez-Jaen, A; Bebek, N; Scudieri, P; Baldassari, S; Salpietro, V; Novelli, G; De Luca, C; von Stulpnagel, C; Kluger, F; Kluger, GJ; Wohlrab, GC; Ramantani, G; Lewis-Smith, D; Thomas, RH; Lai, M; Verrotti, A; Striano, S; Depienne, C; Minetti, C; Benfenati, F; Brancati, F; Zara, F; Striano, P
Neurology. 2021; 97(6):e577-e586
Fallberichte
Safety and efficacy of rufinamide in children and adults with Lennox-Gastaut syndrome: A post hoc analysis from Study 022.
Arzimanoglou, A; Pringsheim, M; Kluger, GJ; Genton, P; Perdomo, C; Malhotra, M
Epilepsy Behav. 2021; 124:108275
Originalarbeiten (Zeitschrift)
Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study.
Grau, J; Zollner, JP; Schubert-Bast, S; Kurlemann, G; Hertzberg, C; Wiemer-Kruel, A; Bast, T; Bertsche, A; Bettendorf, U; Fiedler, B; Hahn, A; Hartmann, H; Hornemann, F; Immisch, I; Jacobs, J; Kieslich, M; Klein, KM; Klotz, KA; Kluger, G; Knuf, M; Mayer, T; Marquard, K; Meyer, S; Muhle, H; Muller-Schluter, K; Noda, AH; Ruf, S; Sauter, M; Schlump, JU; Syrbe, S; Thiels, C; Trollmann, R; Wilken, B; Willems, LM; Rosenow, F; Strzelczyk, A
Orphanet J Rare Dis. 2021; 16(1):282
Originalarbeiten (Zeitschrift)
Epilepsy in Nicolaides-Baraitser Syndrome: Review of Literature and Report of 25 Patients Focusing on Treatment Aspects.
Hofmeister, B; von Stulpnagel, C; Betzler, C; Mari, F; Renieri, A; Baldassarri, M; Haberlandt, E; Jansen, K; Schilling, S; Weber, P; Ahlbory, K; Tang, S; Berweck, S; Kluger, G
Neuropediatrics. 2021; 52(2):109-122
Übersichtsarbeiten
DNA methylation-based classification of malformations of cortical development in the human brain
Jabari, S; Kobow, K; Pieper, T; Hartlieb, T; Kudernatsch, M; Polster, T; Bien, CG; Kalbhenn, T; Simon, M; Hamer, H; Rossler, K; Feucht, M; Muhlebner, A; Najm, I; Peixoto-Santos, JE; Gil-Nagel, A; Delgado, RT; Aledo-Serrano, A; Hou, YH; Coras, R; von Deimling, A; Blumcke, I
ACTA NEUROPATHOL. 2021;
Originalarbeiten (Zeitschrift)
Visual Field Defects before and after pediatric Epilepsy Surgery Clinical Signs, child-oriented Diagnostics, Adaptation before and after Epilepsy Surgery
Neumayr, L; Gschaidmeier, A; Trauzettel-Klosinski, S; Pieper, T; Kudernatsch, M; Hofer, W; Bajer, C; Staudt, M
Z EPILEPTOL. 2021;
Originalarbeiten (Zeitschrift)
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.
Pelletier, F; Perrier, S; Cayami, FK; Mirchi, A; Saikali, S; Tran, LT; Ulrick, N; Guerrero, K; Rampakakis, E; van Spaendonk, RML; Naidu, S; Pohl, D; Gibson, WT; Demos, M; Goizet, C; Tejera-Martin, I; Potic, A; Fogel, BL; Brais, B; Sylvain, M; Sebire, G; Lourenço, CM; Bonkowsky, JL; Catsman-Berrevoets, C; Pinto, PS; Tirupathi, S; Strømme, P; de Grauw, T; Gieruszczak-Bialek, D; Krägeloh-Mann, I; Mierzewska, H; Philippi, H; Rankin, J; Atik, T; Banwell, B; Benko, WS; Blaschek, A; Bley, A; Boltshauser, E; Bratkovic, D; Brozova, K; Cimas, I; Clough, C; Corenblum, B; Dinopoulos, A; Dolan, G; Faletra, F; Fernandez, R; Fletcher, J; Garcia Garcia, ME; Gasparini, P; Gburek-Augustat, J; Gonzalez Moron, D; Hamati, A; Harting, I; Hertzberg, C; Hill, A; Hobson, GM; Innes, AM; Kauffman, M; Kirwin, SM; Kluger, G; Kolditz, P; Kotzaeridou, U; La Piana, R; Liston, E; McClintock, W; McEntagart, M; McKenzie, F; Melançon, S; Misbahuddin, A; Suri, M; Monton, FI; Moutton, S; Murphy, RPJ; Nickel, M; Onay, H; Orcesi, S; Özkınay, F; Patzer, S; Pedro, H; Pekic, S; Pineda Marfa, M; Pizzino, A; Plecko, B; Poll-The, BT; Popovic, V; Rating, D; Rioux, MF; Rodriguez Espinosa, N; Ronan, A; Ostergaard, JR; Rossignol, E; Sanchez-Carpintero, R; Schossig, A; Senbil, N; Sønderberg Roos, LK; Stevens, CA; Synofzik, M; Sztriha, L; Tibussek, D; Timmann, D; Tonduti, D; van de Warrenburg, BP; Vázquez-López, M; Venkateswaran, S; Wasling, P; Wassmer, E; Webster, RI; Wiegand, G; Yoon, G; Rotteveel, J; Schiffmann, R; van der Knaap, M; Vanderver, A; Martos-Moreno, GÁ; Polychronakos, C; Wolf, NI; Bernard, G;
J Clin Endocrinol Metab. 2021; 106(2):e660-e674
Originalarbeiten (Zeitschrift)
Dysmorphic neurons as cellular source for phase-amplitude coupling in Focal Cortical Dysplasia Type II.
Rampp, S; Rössler, K; Hamer, H; Illek, M; Buchfelder, M; Doerfler, A; Pieper, T; Hartlieb, T; Kudernatsch, M; Koelble, K; Peixoto-Santos, JE; Blümcke, I; Coras, R;
Clin Neurophysiol. 2021; 132(3): 782-792.
Originalarbeiten (Zeitschrift)
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.
Stevelink, R; Luykx, JJ; Lin, BD; Leu, C; Lal, D; Smith, AW; Schijven, D; Carpay, JA; Rademaker, K; Rodrigues Baldez, RA; Devinsky, O; Braun, KPJ; Jansen, FE; Smit, DJA; Koeleman, BPC;
Epilepsia. 2021; 62(7): 1518-1527.
Originalarbeiten (Zeitschrift)
Prescription patterns of antiseizure drugs in tuberous sclerosis complex (TSC)-associated epilepsy: a multicenter cohort study from Germany and review of the literature.
Strzelczyk, A; Grau, J; Bast, T; Bertsche, A; Bettendorf, U; Hahn, A; Hartmann, H; Hertzberg, C; Hornemann, F; Immisch, I; Jacobs, J; Klotz, KA; Kluger, G; Knake, S; Knuf, M; Kurlemann, G; Marquard, K; Mayer, T; Meyer, S; Muhle, H; Muller-Schluter, K; von Podewils, F; Rosenow, F; Ruf, S; Sauter, M; Schafer, H; Schlump, JU; Schubert-Bast, S; Syrbe, S; Thiels, C; Trollmann, R; Wiemer-Kruel, A; Wilken, B; Zukunft, B; Zollner, JP
Expert Rev Clin Pharmacol. 2021; 14(6):749-760
Übersichtsarbeiten
Efficacy, tolerability, and retention of fenfluramine for the treatment of seizures in patients with Dravet syndrome: Compassionate use program in Germany.
Strzelczyk, A; Pringsheim, M; Mayer, T; Polster, T; Klotz, KA; Muhle, H; Alber, M; Trollmann, R; Spors, H; Kluger, G; Kurlemann, G; Schubert-Bast, S
Epilepsia. 2021; 62(10):2518-2527
Originalarbeiten (Zeitschrift)
Genetic epilepsies in childhood Exact molecular diagnosis as basis of an individual treatment?
von Stulpnagel, C; Kluger, G
MONATSSCHR KINDERH. 2021;
Originalarbeiten (Zeitschrift)
Childhood Stroke: Long-Term Outcomes and Health-Related Quality of Life with a Special Focus on the Development of Epilepsy.
von Stulpnagel, C; Kutschker, S; Sperl, W; Berweck, S; Staudt, M; Berndt, M; Kluger, G
NEUROPEDIATRICS. 2021; 52(6): 469-474.
Originalarbeiten (Zeitschrift)
Efficacy, Retention and Tolerability of Everolimus in Patients with Tuberous Sclerosis Complex: A Survey-Based Study on Patients" Perspectives.
Willems, LM; Rosenow, F; Schubert-Bast, S; Kurlemann, G; Zollner, JP; Bast, T; Bertsche, A; Bettendorf, U; Ebrahimi-Fakhari, D; Grau, J; Hahn, A; Hartmann, H; Hertzberg, C; Hornemann, F; Immisch, I; Jacobs, J; Klein, KM; Klotz, KA; Kluger, G; Knake, S; Knuf, M; Marquard, K; Mayer, T; Meyer, S; Muhle, H; Muller-Schluter, K; von Podewils, F; Ruf, S; Sauter, M; Schafer, H; Schlump, JU; Syrbe, S; Thiels, C; Trollmann, R; Wiemer-Kruel, A; Wilken, B; Zukunft, B; Strzelczyk, A
CNS DRUGS. 2021; 35(10): 1107-1122.
Originalarbeiten (Zeitschrift)
Health-related quality of life in children and adolescents with tuberous sclerosis complex and their caregivers: A multicentre cohort study from Germany.
Willems, LM; Schubert-Bast, S; Grau, J; Hertzberg, C; Kurlemann, G; Wiemer-Kruel, A; Bast, T; Bertsche, A; Bettendorf, U; Fiedler, B; Hahn, A; Hartmann, H; Hornemann, F; Immisch, I; Jacobs, J; Kieslich, M; Klein, KM; Klotz, KA; Kluger, G; Knuf, M; Mayer, T; Marquard, K; Meyer, S; Muhle, H; Muller-Schluter, K; Noda, AH; Ruf, S; Sauter, M; Schlump, JU; Syrbe, S; Thiels, C; Trollmann, R; Wilken, B; Zollner, JP; Rosenow, F; Strzelczyk, A
EUR J PAEDIATR NEURO. 2021; 35: 111-122.
Originalarbeiten (Zeitschrift)
Next Generation Sequencing in Pediatric Epilepsy Using Customized Panels: Size Matters.
Willimsky, EK; Munzig, A; Mayer, K; Biskup, S; Abicht, A; Hoertnagel, K; von Voss, H; Klein, HG; Rost, I; Larsen, LHG; Dahl, HA; Hoelz, H; von Stuelpnagel, C; Borggraefe, I
Neuropediatrics. 2021; 52(2):92-97
Originalarbeiten (Zeitschrift)
Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency.
Wortmann, SB; Ziętkiewicz, S; Guerrero-Castillo, S; Feichtinger, RG; Wagner, M; Russell, J; Ellaway, C; Mróz, D; Wyszkowski, H; Weis, D; Hannibal, I; von Stülpnagel, C; Cabrera-Orefice, A; Lichter-Konecki, U; Gaesser, J; Windreich, R; Myers, KC; Lorsbach, R; Dale, RC; Gersting, S; Prada, CE; Christodoulou, J; Wolf, NI; Venselaar, H; Mayr, JA; Wevers, RA;
Genet Med. 2021; 23(9): 1705-1714.
Originalarbeiten (Zeitschrift)
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.

Am J Hum Genet. 2021; 108(10):2024
Korrekturen

Publizierte (zitierfähige) Beiträge für wissenschaftliche Veranstaltungen

Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications
Johannesen, KM; Liu, YY; Gjerulfsen, CE; Koko, M; Sonnenberg, L; Schubert, J; Fenger, CD; Eltokhi, A; Rannap, M; Koch, N; Lauxmann, S; Krueger, J; Kegele, J; Canafoglia, L; Franceschetti, S; Mayer, T; Rebstock, J; Zacher, P; Ruf, S; Alber, M; Sterbova, K; Lassuthova, P; Vlckova, M; Lemke, J; Krey, I; Heine, C; Wieczorek, D; Kroell, J; Lund, C; Klein, KM; Au, PB; Rho, J; Ho, A; Masnada, S; Veggiotti, P; Giordano, L; Accorsi, P; Hoi-Hansen, C; Striano, P; Zara, F; Verhelst, H; Verhoeven, JS; van der Zwaag, B; Harder, A; Brilstra, E; Pendziwiat, M; Lebon, S; Vaccarezza, M; Le, NM; Christensen, J; Schmidt-Petersen, M; Gronborg, S; Scherer, S; Howe, J; Fazeli, W; Howell, K; Leventer, R; Stutterd, C; Walsh, S; Gerard, M; Gerard, B; Matricardi, S; Bonardi, CM; Sartori, S; Berger, A; Hoffman-Zacharska, D; Mastrangelo, M; Darra, F; Vollo, A; Motazacker, MM; Lakeman, P; Nizon, M; Betzler, C; Altuzarra, C; Caumes, R; Roubertie, A; Gelisse, P; Marini, C; Guerrini, R; Bilan, F; Koch-Hogrebe, M; Perry, S; Ichikawa, S; Dadali, E; Sharkov, A; Mishina, I; Abramov, M; Kanivets, I; Korostelev, S; Kutsev, S; Wain, KE; Eisenhauer, N; Wagner, M; Savatt, J; Muller-Schluter, K; Bassan, H; Borovikov, A; Nassogne, MC; Destree, A; Schoonjans, AS; Meuwissen, M; Buzatu, M; Jansen, A; Scalais, E; Srivastava, S; Tan, WH; Olson, H; Loddenkemper, T; Poduri, A; Helbig, KL; Helbig, I; Fitzgerald, M; Goldberg, EM; Roser, T; Borggrafe, I; Brunger, T; May, P; Lal, D; Lederer, D; Rubboli, G; Lesca, G; Hedrich, U; Benda, J; Gardella, E; Lerche, H; Moeller, RS
EPILEPSIA. 2021; 62: 34-36.
Abstracts (Zeitschrift)
New-onset refractory status epilepticus (NORSE) and febrile infection-related epilepsy syndrome (FIRES): More differences than similarities
Nausch, E; Schaffeldt, L; Tautorat, I; Margraf, NG; Hausler, M; Kluger, G; Kellinghaus, C; Borzikowsky, C; Laufs, H; van Baalen, A
EPILEPSIA. 2021; 62: 341-341.
Abstracts (Zeitschrift)
Direct and indirect costs and cost drivers of Tuberous sclerosis complex in children, adolescents, and caregivers: A multicenter cohort study
Zollner, JP; Grau, J; Schubert-Bast, S; Kurlemann, G; Hertzberg, C; Wiemer-Kruel, A; Bast, T; Bertsche, A; Bettendorf, U; Fiedler, B; Hahn, A; Hartmann, H; Hornemann, F; Immisch, I; Jacobs-LeVan, J; Kieslich, M; Klein, KM; Klotz, A; Kluger, G; Knuf, M; Mayer, T; Marquard, K; Meyer, S; Noda, AH; Muhle, H; Muller-Schluter, K; Ruf, S; Sauter, M; Schlump, JU; Syrbe, S; Thiels, C; Trollmann, R; Wilken, B; Willems, LM; Rosenow, F; Strzelczyk, A
EPILEPSIA. 2021; 62: 304-305.
Abstracts (Zeitschrift)

2020

Beiträge in Fachzeitschriften

Correlates of intellectual development before and after hemispherotomy: an analysis of 75 children and adolescents.
Bajer, C; Hofer, W; Pieper, T; Kudernatsch, M; Holthausen, H; Staudt, M
EPILEPTIC DISORD. 2020; 22(5): 571-581.
Originalarbeiten (Zeitschrift)
Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration.
Belohlavkova, A; Sterbova, K; Betzler, C; Burkhard, S; Panzer, A; Wolff, M; Lassuthova, P; Vlckova, M; Kyncl, M; Benova, B; Jahodova, A; Kudr, M; Goerg, M; Dusek, P; Seeman, P; Kluger, G; Krsek, P
EUR J PAEDIATR NEURO. 2020; 28: 81-88.
Originalarbeiten (Zeitschrift)
Sudden unexpected death in epilepsy (SUDEP) in children and adolescents-numbers, data and facts
Borusiak, P; Bast, T; Bettendorf, U; Freitag, H; Haberlandt, E; Kluger, G; Springer, S; Wiegand, G
Z EPILEPTOL. 2020;
Übersichtsarbeiten
The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
Doring, JH; Saffari, A; Bast, T; Brockmann, K; Ehrhardt, L; Fazeli, W; Janzarik, WG; Kluger, G; Muhle, H; Moller, RS; Platzer, K; Santos, JL; Bache, I; Bertsche, A; Bonfert, M; Borggrafe, I; Broser, PJ; Datta, AN; Hammer, TB; Hartmann, H; Hasse-Wittmer, A; Henneke, M; Kuhne, H; Lemke, JR; Maier, O; Matzker, E; Merkenschlager, A; Opp, J; Patzer, S; Rostasy, K; Stark, B; Strzelczyk, A; von Stulpnagel, C; Weber, Y; Wolff, M; Zirn, B; Hoffmann, GF; Kolker, S; Syrbe, S
Biomedicines. 2020; 8(11):
Originalarbeiten (Zeitschrift)
ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatment response.
Gasser, M; Boonsimma, P; Netbaramee, W; Wechapinan, T; Srichomthomg, C; Ittiwut, C; Krenn, M; Zimprich, F; Milenkovic, I; Abicht, A; Biskup, S; Roser, T; Shotelersuk, V; Tacke, M; Kuersten, M; Wagner, M; Borggraefe, I; Suphapeetiporn, K; von Stülpnagel, C;
J Clin Neurosci. 2020; 72:31-38
Originalarbeiten (Zeitschrift)
Dog-Assisted Therapy in Neurorehabilitation of Children with Severe Neurological Impairment: An Explorative Study.
Hediger, K; Boek, F; Sachers, J; Blankenburg, U; Antonius-Kluger, E; Rist, B; Schaudek, M; Staudt, M; Kluger, G
NEUROPEDIATRICS. 2020; 51(4): 267-274.
Originalarbeiten (Zeitschrift)
Stability of 0.5% Glucose-Containing Balanced Electrolyte Solutions for Patients on Ketogenic Diets: A Laboratory Study.
Heiderich, S; Dennhardt, N; Hartmann, H; Kluger, GJ; Sümpelmann, R; Herberhold, T;
Neuropediatrics. 2020; 51(6):397-400
Originalarbeiten (Zeitschrift)
Whole-exome and HLA sequencing in Febrile infection-related epilepsy syndrome.
Helbig, I; Barcia, G; Pendziwiat, M; Ganesan, S; Mueller, SH; Helbig, KL; Vaidiswaran, P; Xian, JL; Galer, PD; Afawi, Z; Specchio, N; Kluger, G; Kuhlenbaumer, G; Appenzeller, S; Wittig, M; Kramer, U; van Baalen, A; Nabbout, R
Ann Clin Transl Neurol. 2020; 7(8):1429-1435
Originalarbeiten (Zeitschrift)
Mosaic trisomy of chromosome 1q in human brain tissue associates with unilateral polymicrogyria, very early-onset focal epilepsy, and severe developmental delay.
Kobow, K; Jabari, S; Pieper, T; Kudernatsch, M; Polster, T; Woermann, FG; Kalbhenn, T; Hamer, H; Rossler, K; Muhlebner, A; Spliet, WGM; Feucht, M; Hou, YH; Stichel, D; Korshunov, A; Sahm, F; Coras, R; Blumcke, I; von Deimling, A
Acta Neuropathol. 2020; 140(6):881-891
Originalarbeiten (Zeitschrift)
Antiepileptic therapy approaches in KCNQ2 related epilepsy: A systematic review.
Kuersten, M; Tacke, M; Gerstl, L; Hoelz, H; Stülpnagel, CV; Borggraefe, I;
Eur J Med Genet. 2020; 63(1): 103628
Übersichtsarbeiten
Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study.
Lamberink, HJ; Otte, WM; Blümcke, I; Braun, KPJ;
Lancet Neurol. 2020; 19(9): 748-757.
Originalarbeiten (Zeitschrift)
Presurgical Language fMRI in Children, Adolescents and Young Adults : A Validation Study.
Meinhold, T; Hofer, W; Pieper, T; Kudernatsch, M; Staudt, M;
Clin Neuroradiol. 2020; 30(4):691-704
Originalarbeiten (Zeitschrift)
Cognitive performance and behavior across idiopathic/genetic epilepsies in children and adolescents.
Moorhouse, FJ; Cornell, S; Gerstl, L; Tacke, M; Roser, T; Heinen, F; Bonfert, M; von Stülpnagel, C; Wagner, M; Borggraefe, I;
Sci Rep. 2020; 10(1): 21543
Originalarbeiten (Zeitschrift)
Sacrificing one visual hemifield during pediatric epilepsy surgery: Effects on visual search.
Neumayr, L; Gschaidmeier, A; Trauzettel-Klosinski, S; Pieper, T; Kudernatsch, M; Hofer, W; Bajer, C; Staudt, M
EUR J PAEDIATR NEURO. 2020; 29: 103-107.
Originalarbeiten (Zeitschrift)
Uncovering homonymous visual field defects in candidates for pediatric epilepsy surgery.
Neumayr, L; Pieper, T; Kudernatsch, M; Trauzettel-Klosinski, S; Staudt, M;
EUR J PAEDIATR NEURO. 2020; 25: 165-171.
Originalarbeiten (Zeitschrift)
Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects.
Niestroj, LM; Perez-Palma, E; Howrigan, DP; Zhou, Y; Cheng, F; Saarentaus, E; Nürnberg, P; Stevelink, R; Daly, MJ; Palotie, A; Lal, D;
Brain. 2020; 143(7): 2106-2118.
Originalarbeiten (Zeitschrift)
Expanding the clinical and genetic spectrum of CAD deficiency: an epileptic encephalopathy treatable with uridine supplementation.
Rymen, D; Lindhout, M; Spanou, M; Ashrafzadeh, F; Benkel, I; Betzler, C; Coubes, C; Hartmann, H; Kaplan, JD; Ballhausen, D; Koch, J; Lotte, J; Mohammadi, MH; Rohrbach, M; Dinopoulos, A; Wermuth, M; Willis, D; Brugger, K; Wevers, RA; Boltshauser, E; Bierau, J; Mayr, JA; Wortmann, SB;
Genet Med. 2020; 22(10):1589-1597
Originalarbeiten (Zeitschrift)
Response To: Overlapping Phenotype from Double Trouble SMARCA2 and POLG1 Variants c.2556A > C and c.3708G > T, Respectively.
von Stülpnagel, C; Hofmeister, B; Berweck, S; Kluger, G; Weber, P;
Neuropediatrics. 2020; 51(5):375-376
Letter
Network for Therapy in Rare Epilepsies (NETRE): Lessons From the Past 15 Years.
von Stülpnagel, C; van Baalen, A; Borggraefe, I; Eschermann, K; Hartlieb, T; Kiwull, L; Pringsheim, M; Wolff, M; Kudernatsch, M; Wiegand, G; Striano, P; Kluger, G;
Front Neurol. 2020; 11:622510
Übersichtsarbeiten
Reader response:
Wolf, P; von Stülpnagel, C; Hartlieb, T; Møller, RS; Kluger, GJ;
Neurology. 2020; 94(8): 368-369.
Kommentare
Monogenic variants in dystonia: an exome-wide sequencing study.
Zech, M; Jech, R; Boesch, S; Skorvanek, M; Weber, S; Wagner, M; Zhao, C; Jochim, A; Necpal, J; Dincer, Y; Vill, K; Disteimaier, F; Stoklosa, M; Krenn, M; Grunwald, S; Bock-Bierbaum, T; Fecikova, A; Havrankova, P; Roth, J; Prihodova, I; Adamovicova, M; Ulmanova, O; Bechyne, K; Danhofer, P; Vesely, B; Han, V; Pavelekova, P; Gdovinova, Z; Mantel, T; Meindl, T; Sitzberger, A; Schroder, S; Blaschek, A; Roser, T; Bonfert, M; Haberlandt, E; Plecko, B; Leineweber, B; Berweck, S; Herberhold, T; Langguth, B; Svantnerova, J; Minar, M; Ramos-Rivera, GA; Wojcik, MH; Pajusalu, S; Ounap, K; Schatz, UA; Polsler, L; Milenkovic, I; Laccone, F; Pilhofer, V; Colombo, R; Patzer, S; Iuso, A; Vera, J; Troncoso, M; Fang, F; Prokisch, H; Wilbert, F; Eckenweiler, M; Graf, E; Westphal, DS; Riedhammer, KM; Brunet, T; Alhaddad, B; Berutti, R; Strom, TM; Hecht, M; Baumann, M; Wolf, M; Telegrafi, A; Person, RE; Zamora, FM; Henderson, LB; Weise, D; Musacchio, T; Volkmann, J; Szuto, A; Becker, J; Cremer, K; Sycha, T; Zimprich, F; Kraus, V; Makowski, C; Gonzalez-Alegre, P; Bardakjian, TM; Ozelius, LJ; Vetro, A; Guerrini, R; Maier, E; Borggraefe, I; Kuster, A; Wortmann, SB; Hackenberg, A; Steinfeld, R; Assmann, B; Staufner, C; Opladen, T; Ruzicka, E; Cohn, RD; Dyment, D; Chung, WK; Engels, H; Ceballos-Baumann, A; Ploski, R; Daumke, O; Haslinger, B; Mall, V; Oexle, K; Winkehnann, J
LANCET NEUROL. 2020; 19(11): 908-918.
Originalarbeiten (Zeitschrift)

2019

Beiträge in Fachzeitschriften

Age-related MR characteristics in mild malformation of cortical development with oligodendroglial hyperplasia and epilepsy (MOGHE).
Hartlieb, T; Winkler, P; Coras, R; Pieper, T; Holthausen, H; Blümcke, I; Staudt, M; Kudernatsch, M;
Epilepsy Behav. 2019; 91:68-74
Originalarbeiten (Zeitschrift)
Clinical characteristics, resource utilization, quality of life and care situation for patients with Dravet syndrome in Germany
Kalski, M; Schubert-Bast, S; Kieslich, M; Leyer, AC; Polster, T; Herting, A; Mayer, T; Trollmann, R; Neubauer, BA; Bettendorf, U; Bast, T; Wiemer-Kruel, A; von Spiczak, S; Kurlemann, G; Wolff, M; Kluger, G; Carroll, J; Macdonald, D; Pritchard, C; Irwin, J; Klein, KM; Rosenow, F; Strzelczyk, A; Kay, L
Z EPILEPTOL. 2019;
Originalarbeiten (Zeitschrift)
Positive Short-Term Effect of Low-Dose Rosuvastatin in a Patient with SYNGAP1-Associated Epilepsy.
Kluger, G; von Stulpnagel-Steinbeis, C; Arnold, S; Eschermann, K; Hartlieb, T
NEUROPEDIATRICS. 2019; 50(4): 266-267.
Letter
Unresponsive Wakefulness Syndrome in Children after Near-Drowning: Long-Term Outcome and Impact on the Families.
Kluger, GJ; Kirsch, A; Hessenauer, M; Aust, H; Berweck, S; Sperl, W; Betzler, C; von Stülpnagel-Steinbeis, C; Staudt, M;
Neuropediatrics. 2019; 50(2):71-79
Originalarbeiten (Zeitschrift)
Genomic DNA methylation distinguishes subtypes of human focal cortical dysplasia.
Kobow, K; Ziemann, M; Kaipananickal, H; Khurana, I; Mühlebner, A; Feucht, M; Hainfellner, JA; Czech, T; Aronica, E; Pieper, T; Holthausen, H; Kudernatsch, M; Hamer, H; Kasper, BS; Rössler, K; Conti, V; Guerrini, R; Coras, R; Blümcke, I; El-Osta, A; Kaspi, A;
Epilepsia. 2019; 60(6):109-1103
Originalarbeiten (Zeitschrift)
Dravet-Syndrom und Impfung — epileptologische, genetische und gutachtliche Aspekte
Kusnik, B; Lorenz, M; Kleiser, B; Kluger, G;
Der medizinische Sachverständige. 2019;
Originalarbeiten (Zeitschrift)
The development of the expressive speech after surgery in Broca ’s area in two-year-old child: А case report Развитие экспрессивной речи после хирургической резекции лобной доли с включением зоны Брока у ребенка 2 лет: клинический случай
Moiseeva, SL; Hartlieb, T; Winkler, P; Kudernatsch, M; Staudt, M;
Russian journal of child neurology. 2019; 14(2): 49-52.
Fallberichte
Structural brain anomalies in patients with FOXG1 syndrome and in Foxg1+/- mice.
Pringsheim, M; Mitter, D; Schroder, S; Warthemann, R; Plumacher, K; Kluger, G; Baethmann, M; Bast, T; Braun, S; Buttel, HM; Conover, E; Courage, C; Datta, AN; Eger, A; Grebe, TA; Hasse-Wittmer, A; Heruth, M; Hoft, K; Kaindl, AM; Karch, S; Kautzky, T; Korenke, GC; Kruse, B; Lutz, RE; Omran, H; Patzer, S; Philippi, H; Ramsey, K; Rating, T; Riess, A; Schimmel, M; Westman, R; Zech, FM; Zirn, B; Ulmke, PA; Sokpor, G; Tuoc, T; Leha, A; Staudt, M; Brockmann, K
ANN CLIN TRANSL NEUR. 2019; 6(4): 655-668.
Originalarbeiten (Zeitschrift)
Seizure management and prescription patterns of anticonvulsants in Dravet syndrome: A multicenter cohort study from Germany and review of literature.
Schubert-Bast, S; Wolff, M; Wiemer-Kruel, A; von Spiczak, S; Trollmann, R; Reif, PS; Pritchard, C; Polster, T; Neubauer, BA; Mayer, T; Macdonald, D; Kurlemann, G; Kluger, G; Klein, KM; Kieslich, M; Kay, L; Kalski, M; Irwin, J; Herting, A; Carroll, J; Bettendorf, U; Bast, T; Rosenow, F; Strzelczyk, A
EPILEPSY BEHAV. 2019; 98(Pt A): 88-95.
Übersichtsarbeiten
Clinical and genetic spectrum of SCN2A-associated episodic ataxia.
Schwarz, N; Bast, T; Gaily, E; Golla, G; Gorman, KM; Griffiths, LR; Hahn, A; Hukin, J; King, M; Korff, C; Miranda, MJ; Moller, RS; Neubauer, B; Smith, RA; Smol, T; Striano, P; Stroud, B; Vaccarezza, M; Kluger, G; Lerche, H; Fazeli, W
EUR J PAEDIATR NEURO. 2019; 23(3): 438-447.
Originalarbeiten (Zeitschrift)
Electrode placement accuracy in robot-assisted epilepsy surgery: A comparison of different referencing techniques including frame-based CT versus facial laser scan based on CT or MRI.
Spyrantis, A; Cattani, A; Woebbecke, T; Konczalla, J; Strzelczyk, A; Rosenow, F; Wagner, M; Seifert, V; Kudernatsch, M; Freiman, TM;
Epilepsy Behav. 2019; 91:38-47
Originalarbeiten (Zeitschrift)
A multicenter, matched case-control analysis comparing burden-of-illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany.
Strzelczyk, A; Schubert-Bast, S; Bast, T; Bettendorf, U; Fiedler, B; Hamer, HM; Herting, A; Kalski, M; Kay, L; Kieslich, M; Klein, KM; Kluger, G; Kurlemann, G; Mayer, T; Neubauer, BA; Polster, T; von Spiczak, S; Stephani, U; Trollmann, R; Wiemer-Kruel, A; Wolff, M; Irwin, J; Carroll, J; Pritchard, C; Rosenow, F
EPILEPSIA. 2019; 60(8): 1697-1710.
Originalarbeiten (Zeitschrift)
Mesial Temporal Sclerosis in SCN1A-Related Epilepsy: Two Long-Term EEG Case Studies.
Tiefes, AM; Hartlieb, T; Tacke, M; von Stülpnagel-Steinbeis, C; Larsen, LHG; Hao, Q; Dahl, HA; Neubauer, BA; Gerstl, L; Kudernatsch, M; Kluger, GJ; Borggraefe, I;
Clin EEG Neurosci. 2019; 50(4): 26-272.
Fallberichte
Chewing induced reflex seizures ("eating epilepsy") and eye closure sensitivity as a common feature in pediatric patients with SYNGAP1 mutations: Review of literature and report of 8 cases.
von Stülpnagel, C; Hartlieb, T; Borggräfe, I; Coppola, A; Gennaro, E; Eschermann, K; Kiwull, L; Kluger, F; Krois, I; Møller, RS; Rössler, F; Santulli, L; Schwermer, C; Wallacher-Scholz, B; Zara, F; Wolf, P; Kluger, G;
Seizure. 2019; 65:-137
Originalarbeiten (Zeitschrift)
Clinical spectrum of
Wolking, S; May, P; Mei, D; Moller, RS; Balestrini, S; Helbig, KL; Altuzarra, CD; Chatron, N; Kaiwar, C; Stohr, K; Widdess-Walsh, P; Mendelsohn, BA; Numis, A; Cilio, MR; Van Paesschen, W; Svendsen, LL; Oates, S; Hughes, E; Goyal, S; Brown, K; Saenz, MS; Dorn, T; Muhle, H; Pagnamenta, AT; Vavoulis, DV; Knight, SJL; Taylor, JC; Canevini, MP; Darra, F; Gavrilova, RH; Powis, Z; Tang, S; Marquetand, J; Armstrong, M; McHale, D; Klee, EW; Kluger, GJ; Lowenstein, DH; Weckhuysen, S; Pal, DK; Helbig, I; Guerrini, R; Thomas, RH; Rees, MI; Lesca, G; Sisodiya, SM; Weber, YG; Lal, D; Marini, C; Lerche, H; Schubert, J
NEUROLOGY. 2019; 92(11): e1238-e1249.
Originalarbeiten (Zeitschrift)

Publizierte (zitierfähige) Beiträge für wissenschaftliche Veranstaltungen

Comparative Socioeconomic Study Of Patients In Germany With Dravet Syndrome, Refractory Epilepsy Or Epilepsy In Seizure Remission, And Their Caregivers
Strzelczyk, A; Schubert-Bast, S; Bast, T; Bettendorf, U; Hamer, HM; Herting, A; Kalski, M; Kay, L; Kieslich, M; Klein, KM; Kluger, G; Kurlemann, G; Mayer, T; Neubauer, BA; Polster, T; von Spiczak, S; Stephani, U; Trollmann, R; Wiemer-Kruel, A; Wolff, M; Irwin, J; Carroll, J; Pritchard, C; Rosenow, F
EPILEPSIA. 2019; 60: 195-196.
Abstracts (Zeitschrift)

2018

Beiträge in Fachzeitschriften

Pediatric Klüver-Bucy Syndrome: Report of Two Cases and Review of the Literature.
Kluger, G; Romein, E; Hessenauer, M; Pringsheim, M; Berweck, S
NEUROPEDIATRICS. 2018; 49(5): 353-354.
Letter
Die Tiefe Hirnstimulation bei medikamentös therapieschwieriger Epilepsie
Kudernatsch, M; Arnold, S;
Das Neurophysiologie-Labor. 2018; 189-198.
Originalarbeiten (Zeitschrift)
Seizure Freedom in Patients with Dravet Syndrome with Contraceptives: A Case Report with Two Patients
Lotte, J; Grothe, S; Kluger, GJ
NEUROPEDIATRICS. 2018; 49(4): 276-278.
Fallberichte
FOXG1 syndrome: genotype-phenotype association in 83 patients with FOXG1 variants.
Mitter, D; Pringsheim, M; Kaulisch, M; Plümacher, KS; Schröder, S; Warthemann, R; Abou Jamra, R; Baethmann, M; Bast, T; Büttel, HM; Cohen, JS; Conover, E; Courage, C; Eger, A; Fatemi, A; Grebe, TA; Hauser, NS; Heinritz, W; Helbig, KL; Heruth, M; Huhle, D; Höft, K; Karch, S; Kluger, G; Korenke, GC; Lemke, JR; Lutz, RE; Patzer, S; Prehl, I; Hoertnagel, K; Ramsey, K; Rating, T; Rieß, A; Rohena, L; Schimmel, M; Westman, R; Zech, FM; Zoll, B; Malzahn, D; Zirn, B; Brockmann, K;
Genet Med. 2018; 20(1): 98-108.
Originalarbeiten (Zeitschrift)
Identifying the educational needs of physicians in pediatric epilepsy in order to improve care: results from a needs assessment in Germany, Spain, and the United States.
Murray, S; Labbe, S; Kothare, S; Malaga, I; Kluger, G; Ogden, P; Lazure, P; Arzimanoglou, A
EPILEPTIC DISORD. 2018; 20(4): 239-256.
Originalarbeiten (Zeitschrift)
Virtual Reality for Neurorehabilitation: Insights From 3 European Clinics.
ONeil, O; Fernandez, MM; Herzog, J; Beorchia, M; Gower, V; Gramatica, F; Starrost, K; Kiwull, L;
PM R. 2018; 10(9 Suppl 2):S198-S206
Übersichtsarbeiten
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; 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; Kuhne, H; Kurlemann, G; Mandl, M; Mause, U; Navratil, P; Opp, J; Penzien, J; Prietsch, V; Quattlander, A; Rating, D; Schara, U; Shamdeen, MG; Sprinz, A; Wendker-Magrabi, H; Stephani, U; Muhle, H; Strassburg, HM; Topke, B; Trollmann, R; Tuschen-Hofstatter, E; Waltz, S; Weber, G; Wien, FU; Wolffxxx, M; Polster, T; Freitag, H; Sonmez, O; Reinhardt, K; Traus, M; Hoovey, Z
SEIZURE-EUR J EPILEP. 2018; 56: 115-120.
Originalarbeiten (Zeitschrift)
Absence Seizures as a Feature of Juvenile Myoclonic Epilepsy in Rhodesian Ridgeback Dogs.
Wielaender, F; James, FMK; Cortez, MA; Kluger, G; Neßler, JN; Tipold, A; Lohi, H; Fischer, A;
J Vet Intern Med. 2018; 32(1):428-432
Fallberichte
Neurologic phenotypes associated with
Zagaglia, S; Selch, C; Nisevic, JR; Mei, D; Michalak, Z; Hernandez-Hernandez, L; Krithika, S; Vezyroglou, K; Varadkar, SM; Pepler, A; Biskup, S; Leão, M; Gärtner, J; Merkenschlager, A; Jaksch, M; Møller, RS; Gardella, E; Kristiansen, BS; Hansen, LK; Vari, MS; Helbig, KL; Desai, S; Smith-Hicks, CL; Hino-Fukuyo, N; Talvik, T; Laugesaar, R; Ilves, P; Õunap, K; Körber, I; Hartlieb, T; Kudernatsch, M; Winkler, P; Schimmel, M; Hasse, A; Knuf, M; Heinemeyer, J; Makowski, C; Ghedia, S; Subramanian, GM; Striano, P; Thomas, RH; Micallef, C; Thom, M; Werring, DJ; Kluger, GJ; Cross, JH; Guerrini, R; Balestrini, S; Sisodiya, SM;
Neurology. 2018; 91(22):e207-e2088
Originalarbeiten (Zeitschrift)

Publizierte (zitierfähige) Beiträge für wissenschaftliche Veranstaltungen

Chewing Induced Reflex Seizures ("Eating Epilepsy") as A New Additional Clinical Feature in Pediatric Patients with SYNGAP1 Mutations? Review of Literature and Case Report
Eschermann, K; Kiwull, L; Stulpnagel, CV; Hartlieb, T; Kluger, F; Kluger, G
EPILEPSIA. 2018; 59: S293-S293.
Abstracts (Zeitschrift)
Histopathology And Mri Findings In Two Children With COL4A1/-2 Mutation Related Epilepsy
Koerber, I; Kudernatsch, M; Hartlieb, T; Selch, C; Sisodiya, S; Coras, R; Blumcke, I; Winkler, P; Berweck, S; Kluger, G
EPILEPSIA. 2018; 59: S188-S188.
Abstracts (Zeitschrift)

Originalbeiträge in Sammelwerk (Buchbeitrag)

Kapitel zu Epilepsie nach kindlichem Schlaganfall
von Stülpnagel-Steinbeis, C;
In: Gerstl und Ingo Borggräfe (Hrsg) editors(s). Pediatric Stroke Manual (Pädiatrische Neurologie) Lucia.

2017

Beiträge in Fachzeitschriften

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery.
Blumcke, I; Spreafico, R; Haaker, G; Coras, R; Kobow, K; Bien, CG; Pfäfflin, M; Elger, C; Widman, G; Schramm, J; Becker, A; Braun, KP; Leijten, F; Baayen, JC; Aronica, E; Chassoux, F; Hamer, H; Stefan, H; Rössler, K; Thom, M; Walker, MC; Sisodiya, SM; Duncan, JS; McEvoy, AW; Pieper, T; Holthausen, H; Kudernatsch, M; Meencke, HJ; Kahane, P; Schulze-Bonhage, A; Zentner, J; Heiland, DH; Urbach, H; Steinhoff, BJ; Bast, T; Tassi, L; Lo Russo, G; Özkara, C; Oz, B; Krsek, P; Vogelgesang, S; Runge, U; Lerche, H; Weber, Y; Honavar, M; Pimentel, J; Arzimanoglou, A; Ulate-Campos, A; Noachtar, S; Hartl, E; Schijns, O; Guerrini, R; Barba, C; Jacques, TS; Cross, JH; Feucht, M; Mühlebner, A; Grunwald, T; Trinka, E; Winkler, PA; Gil-Nagel, A; Toledano Delgado, R; Mayer, T; Lutz, M; Zountsas, B; Garganis, K; Rosenow, F; Hermsen, A; von Oertzen, TJ; Diepgen, TL; Avanzini, G;
N Engl J Med. 2017; 377(17):1648-1656
Originalarbeiten (Zeitschrift)
Early seizures predict the development of epilepsy in children and adolescents with stroke.
Breitweg, I; Stülpnagel, CV; Pieper, T; Lidzba, K; Holthausen, H; Staudt, M; Kluger, G;
Eur J Paediatr Neurol. 2017; 21(3): 465-467.
Originalarbeiten (Zeitschrift)
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
Depienne, C; Nava, C; Keren, B; Heide, S; Rastetter, A; Passemard, S; Chantot-Bastaraud, S; Moutard, ML; Agrawal, PB; VanNoy, G; Stoler, JM; Amor, DJ; Billette de Villemeur, T; Doummar, D; Alby, C; Cormier-Daire, V; Garel, C; Marzin, P; Scheidecker, S; de Saint-Martin, A; Hirsch, E; Korff, C; Bottani, A; Faivre, L; Verloes, A; Orzechowski, C; Burglen, L; Leheup, B; Roume, J; Andrieux, J; Sheth, F; Datar, C; Parker, MJ; Pasquier, L; Odent, S; Naudion, S; Delrue, MA; Le Caignec, C; Vincent, M; Isidor, B; Renaldo, F; Stewart, F; Toutain, A; Koehler, U; Häckl, B; von Stülpnagel, C; Kluger, G; Møller, RS; Pal, D; Jonson, T; Soller, M; Verbeek, NE; van Haelst, MM; de Kovel, C; Koeleman, B; Monroe, G; van Haaften, G; Attié-Bitach, T; Boutaud, L; Héron, D; Mignot, C;
Hum Genet. 2017; 136(4): 463-479.
Originalarbeiten (Zeitschrift)
CAD mutations and uridine-responsive epileptic encephalopathy.
Koch, J; Mayr, JA; Alhaddad, B; Rauscher, C; Bierau, J; Kovacs-Nagy, R; Coene, KL; Bader, I; Holzhacker, M; Prokisch, H; Venselaar, H; Wevers, RA; Distelmaier, F; Polster, T; Leiz, S; Betzler, C; Strom, TM; Sperl, W; Meitinger, T; Wortmann, SB; Haack, TB;
Brain. 2017; 140(Pt 2): 279-286.
Originalarbeiten (Zeitschrift)
Dosing considerations for rufinamide in patients with Lennox-Gastaut syndrome: Phase III trial results and real-world clinical data.
Kothare, S; Kluger, G; Sachdeo, R; Williams, B; Olhaye, O; Perdomo, C; Bibbiani, F
SEIZURE-EUR J EPILEP. 2017; 47: 25-33.
Originalarbeiten (Zeitschrift)
The time window for successful right-hemispheric language reorganization in children
Lidzba, K; Kupper, H; Kluger, G; Staudt, B
EUR J PAEDIATR NEURO. 2017; 21(5): 715-721.
Originalarbeiten (Zeitschrift)
Mutations in GABRB3: From febrile seizures to epileptic encephalopathies.
Møller, RS; Wuttke, TV; Helbig, I; Marini, C; Johannesen, KM; Brilstra, EH; Vaher, U; Borggraefe, I; Talvik, I; Talvik, T; Kluger, G; Francois, LL; Lesca, G; de Bellescize, J; Blichfeldt, S; Chatron, N; Holert, N; Jacobs, J; Swinkels, M; Betzler, C; Syrbe, S; Nikanorova, M; Myers, CT; Larsen, LH; Vejzovic, S; Pendziwiat, M; von Spiczak, S; Hopkins, S; Dubbs, H; Mang, Y; Mukhin, K; Holthausen, H; van Gassen, KL; Dahl, HA; Tommerup, N; Mefford, HC; Rubboli, G; Guerrini, R; Lemke, JR; Lerche, H; Muhle, H; Maljevic, S;
Neurology. 2017; 88(5): 483-492.
Originalarbeiten (Zeitschrift)
Mild Malformation of Cortical Development with Oligodendroglial Hyperplasia in Frontal Lobe Epilepsy: A New Clinico-Pathological Entity.
Schurr, J; Coras, R; Rössler, K; Pieper, T; Kudernatsch, M; Holthausen, H; Winkler, P; Woermann, F; Bien, CG; Polster, T; Schulz, R; Kalbhenn, T; Urbach, H; Becker, A; Grunwald, T; Huppertz, HJ; Gil-Nagel, A; Toledano, R; Feucht, M; Mühlebner, A; Czech, T; Blümcke, I;
Brain Pathol. 2017; 27(1):26-35
Originalarbeiten (Zeitschrift)
Febrile Infection-Related Epilepsy Syndrome: Clinical Review and Hypotheses of Epileptogenesis.
van Baalen, A; Vezzani, A; Häusler, M; Kluger, G;
Neuropediatrics. 2017; 48(1):5-18
Originalarbeiten (Zeitschrift)
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs.
von Stülpnagel, C; Ensslen, M; Møller, RS; Pal, DK; Masnada, S; Veggiotti, P; Piazza, E; Dreesmann, M; Hartlieb, T; Herberhold, T; Hughes, E; Koch, M; Kutzer, C; Hoertnagel, K; Nitanda, J; Pohl, M; Rostásy, K; Haack, TB; Stöhr, K; Kluger, G; Borggraefe, I;
Eur J Paediatr Neurol. 2017; 21(3): 530-541.
Originalarbeiten (Zeitschrift)
Generalized myoclonic epilepsy with photosensitivity in juvenile dogs caused by a defective DIRAS family GTPase 1.
Wielaender, F; Sarviaho, R; James, F; Hytonen, MK; Cortez, MA; Kluger, G; Koskinen, LLE; Arumilli, M; Kornberg, M; Bathen-Noethen, A; Tipold, A; Rentmeister, K; Bhatti, SFM; Hulsmeyer, V; Boettcher, IC; Tastensen, C; Flegel, T; Dietschi, E; Leeb, T; Matiasek, K; Fischer, A; Lohi, H
P NATL ACAD SCI USA. 2017; 114(10): 2669-2674.
Originalarbeiten (Zeitschrift)
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders
Wolff, M; Johannesen, KM; Hedrich, UBS; Masnada, S; Rubboli, G; Gardella, E; Lesca, G; Ville, D; Milh, M; Villard, L; Afenjar, A; Chantot-Bastaraud, S; Mignot, C; Lardennois, C; Nava, C; Schwarz, N; Gerard, M; Perrin, L; Doummar, D; Auvin, S; Miranda, MJ; Hempel, M; Brilstra, E; Knoers, N; Verbeek, N; van Kempen, M; Braun, KP; Mancini, G; Biskup, S; Hortnagel, K; Docker, M; Bast, T; Loddenkemper, T; Wong-Kisiel, L; Baumeister, FM; Fazeli, W; Striano, P; Dilena, R; Fontana, E; Zara, F; Kurlemann, G; Klepper, J; Thoene, JG; Arndt, DH; Deconinck, N; Schmitt-Mechelke, T; Maier, O; Muhle, H; Wical, B; Finetti, C; Bruckner, R; Pietz, J; Golla, G; Jillella, D; Linnet, KM; Charles, P; Moog, U; Oiglane-Shlik, E; Mantovani, JF; Park, K; Deprez, M; Lederer, D; Mary, S; Scalais, E; Selim, L; Van Coster, R; Lagae, L; Nikanorova, M; Hjalgrim, H; Korenke, GC; Trivisano, M; Specchio, N; Ceulemans, B; Dorn, T; Helbig, KL; Hardies, K; Stamberger, H; de Jonghe, P; Weckhuysen, S; Lemke, JR; Krageloh-Mann, I; Helbig, I; Kluger, G; Lerche, H; Moller, RS
BRAIN. 2017; 140: 1316-1336.
Originalarbeiten (Zeitschrift)

2016

Beiträge in Fachzeitschriften

A longitudinal, randomized, and prospective study of nocturnal monitoring in children and adolescents with epilepsy: Effects on quality of life and sleep
Borusiak, P; Bast, T; Kluger, G; Weidenfeld, A; Langer, T; Jenke, ACW; Wiegand, G
EPILEPSY BEHAV. 2016; 61: 192-198.
Originalarbeiten (Zeitschrift)
Autoantibodies to neuronal antigens in children with focal epilepsy and no prima facie signs of encephalitis.
Borusiak, P; Bettendorf, U; Wiegand, G; Bast, T; Kluger, G; Philippi, H; Munstermann, D; Bien, CG
EUR J PAEDIATR NEURO. 2016; 20(4): 573-579.
Originalarbeiten (Zeitschrift)
Predicting hand function after hemidisconnection.
Küpper, H; Kudernatsch, M; Pieper, T; Groeschel, S; Tournier, JD; Raffelt, D; Winkler, P; Holthausen, H; Staudt, M;
Brain. 2016; 139(Pt 9):245-268
Originalarbeiten (Zeitschrift)
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Li, D; Yuan, HJ; Ortiz-Gonzalez, XR; Marsh, ED; Tian, LF; McCormick, EM; Kosobucki, GJ; Chen, WJ; Schulien, AJ; Chiavacci, R; Tankovic, A; Naase, C; Brueckner, F; von Stulpnagel-Steinbeis, C; Hu, C; Kusumoto, H; Hedrich, UBS; Elsen, G; Hortnagel, K; Aizenman, E; Lemke, JR; Hakonarson, H; Traynelis, SF; Falk, MJ
AM J HUM GENET. 2016; 99(4): 802-816.
Originalarbeiten (Zeitschrift)
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations.
Lotte, J; Bast, T; Borusiak, P; Coppola, A; Cross, JH; Dimova, P; Fogarasi, A; Graness, I; Guerrini, R; Hjalgrim, H; Keimer, R; Korff, CM; Kurlemann, G; Leiz, S; Linder-Lucht, M; Loddenkemper, T; Makowski, C; Muhe, C; Nicolai, J; Nikanorova, M; Pellacani, S; Philip, S; Ruf, S; Fernandez, IS; Schlachter, K; Striano, P; Sukhudyan, B; Valcheva, D; Vermeulen, RJ; Weisbrod, T; Wilken, B; Wolf, P; Kluger, G
Seizure. 2016; 35:106-110
Originalarbeiten (Zeitschrift)
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
Mignot, C; von Stulpnagel, C; Nava, C; Ville, D; Sanlaville, D; Lesca, G; Rastetter, A; Gachet, B; Marie, Y; Korenke, GC; Borggraefe, I; Hoffmann-Zacharska, D; Szczepanik, E; Rudzka-Dybala, M; Yis, U; Caglayan, H; Isapof, A; Marey, I; Panagiotakaki, E; Korff, C; Rossier, E; Riess, A; Beck-Woedl, S; Rauch, A; Zweier, C; Hoyer, J; Reis, A; Mironov, M; Bobylova, M; Mukhin, K; Hernandez-Hernandez, L; Maher, B; Sisodiya, S; Kuhn, M; Glaeser, D; Wechuysen, S; Myers, CT; Mefford, HC; Hortnagel, K; Biskup, S; Lemke, JR; Heron, D; Kluger, G; Depienne, C
J MED GENET. 2016; 53(8): 511-522.
Originalarbeiten (Zeitschrift)
Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5-related epilepsy.
Müller, A; Helbig, I; Jansen, C; Bast, T; Guerrini, R; Jähn, J; Muhle, H; Auvin, S; Korenke, GC; Philip, S; Keimer, R; Striano, P; Wolf, NI; Püst, B; Thiels, C; Fogarasi, A; Waltz, S; Kurlemann, G; Kovacevic-Preradovic, T; Ceulemans, B; Schmitt, B; Philippi, H; Tarquinio, D; Buerki, S; von Stülpnagel, C; Kluger, G;
Eur J Paediatr Neurol. 2016; 20(1):147-151
Originalarbeiten (Zeitschrift)
STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy.
Stamberger, H; Nikanorova, M; Willemsen, MH; Accorsi, P; Angriman, M; Baier, H; Benkel-Herrenbrueck, I; Benoit, V; Budetta, M; Caliebe, A; Cantalupo, G; Capovilla, G; Casara, G; Courage, C; Deprez, M; Destree, A; Dilena, R; Erasmus, CE; Fannemel, M; Fjaer, R; Giordano, L; Helbig, KL; Heyne, HO; Klepper, J; Kluger, GJ; Lederer, D; Lodi, M; Maier, O; Merkenschlager, A; Michelberger, N; Minetti, C; Muhle, H; Phalin, J; Ramsey, K; Romeo, A; Schallner, J; Schanze, I; Shinawi, M; Sleegers, K; Sterbova, K; Syrbe, S; Traverso, M; Tzschach, A; Uldall, P; Van Coster, R; Verhelst, H; Viri, M; Winter, S; Wolff, M; Zenker, M; Zoccante, L; De Jonghe, P; Helbig, I; Striano, P; Lemke, JR; Moller, RS; Weckhuysen, S
Neurology. 2016; 86(10):954-962
Übersichtsarbeiten
MRI-imaging and clinical findings of eleven children with tick-borne encephalitis and review of the literature.
von Stülpnagel, C; Winkler, P; Koch, J; Zeches-Kansy, C; Schöttler-Glas, A; Wolf, G; Niller, HH; Staudt, M; Kluger, G; Rostasy, K;
Eur J Paediatr Neurol. 2016; 20(1):45-52
Originalarbeiten (Zeitschrift)

2015

Beiträge in Fachzeitschriften

Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies: first experiences.
Biro, A; Stephani, U; Tarallo, T; Bast, T; Schlachter, K; Fleger, M; Kurlemann, G; Fiedler, B; Leiz, S; Nikanorova, M; Wolff, M; Muller, A; Selch, C; Staudt, M; Kluger, G
NEUROPEDIATRICS. 2015; 46(2): 110-115.
Originalarbeiten (Zeitschrift)
EPILEPSY SURGERY IN PATIENTS WITH TUBEROUS SCLEROSIS Хирургическое лечение эпилепсии у пациентов с туберозным склерозом
Holthausen, H; Pieper, T; Eitel, H; , Kudernatsch, M;
Russian journal of child neurology. 2015; 10 (1)(40):
Originalarbeiten (Zeitschrift)
47 patients with FLNA associated periventricular nodular heterotopia.
Lange, M; Kasper, B; Bohring, A; Rutsch, F; Kluger, G; Hoffjan, S; Spranger, S; Behnecke, A; Ferbert, A; Hahn, A; Oehl-Jaschkowitz, B; Graul-Neumann, L; Diepold, K; Schreyer, I; Bernhard, MK; Mueller, F; Siebers-Renelt, U; Beleza-Meireles, A; Uyanik, G; Janssens, S; Boltshauser, E; Winkler, J; Schuierer, G; Hehr, U
ORPHANET J RARE DIS. 2015; 10: 134
Originalarbeiten (Zeitschrift)
Glutamate-mediated upregulation of the multidrug resistance protein 2 in porcine and human brain capillaries.
Luna-Munguia, H; Salvamoser, JD; Pascher, B; Pieper, T; Getzinger, T; Kudernatsch, M; Kluger, G; Potschka, H;
J Pharmacol Exp Ther. 2015; 352(2):36-78
Originalarbeiten (Zeitschrift)
Glutamate-Mediated Down-Regulation of the Multidrug-Resistance Protein BCRP/ABCG2 in Porcine and Human Brain Capillaries.
Salvamoser, JD; Avemary, J; Luna-Munguia, H; Pascher, B; Getzinger, T; Pieper, T; Kudernatsch, M; Kluger, G; Potschka, H;
Mol Pharm. 2015; 12(6):2049-2060
Originalarbeiten (Zeitschrift)
SYNGAP1 Mutation in Focal and Generalized Epilepsy: A Literature Overview and A Case Report with Special Aspects of the EEG.
von Stulpnagel, C; Funke, C; Haberl, C; Hortnagel, K; Jungling, J; Weber, YG; Staudt, M; Kluger, G
NEUROPEDIATRICS. 2015; 46(4): 287-291.
Fallberichte

2014

Beiträge in Fachzeitschriften

Use of intrathecal baclofen in children and adolescents: interdisciplinary consensus table 2013.
Berweck, S; Lütjen, S; Voss, W; Diebold, U; Mücke, KH; Aisch, A; Ostertag, B; Friedrich, M; Wagner, C; Kudernatsch, M; Granel, M; Kluger, G; Ludwikowski, B; Peraud, A; Rauchenzauner, M; Schroeder, AS; Sprinz, A; Wienand, R; Wilken, B; Kästner, S; Zeches, C; Mall, V;
Neuropediatrics. 2014; 45(5):294-308
Originalarbeiten (Zeitschrift)
Electro-clinical-pathological correlations in focal cortical dysplasia (FCD) at young ages.
Holthausen, H; Pieper, T; Winkler, P; Bluemcke, I; Kudernatsch, M;
Childs Nerv Syst. 2014; 30(12):2015-2026
Übersichtsarbeiten

Publizierte (zitierfähige) Beiträge für wissenschaftliche Veranstaltungen

RETROSPECTIVE EVALUATION OF ANTIEPILEPTIC DRUGS AND KETOGENIC DIET IN 40 PATIENTS WITH CDKL5 MUTATIONS: LOW LONG-TERM EFFICACY
Muller, A; Jansen, C; Selch, C; Bast, T; Lotte, J; Guerrini, R; Albers, J; Muhle, H; Auvin, S; Korenke, GC; Philip, S; Keimer, R; Striano, P; Wolf, NI; Puest, B; Thiels, C; Fogarasi, A; Waltz, S; Kurlemann, G; Kovacevic-Preradovic, T; Ceulemans, B; Berweck, S; Staudt, M; Kluger, G
EPILEPSIA. 2014; 55: 178-179.
Abstracts (Zeitschrift)

2013

Beiträge in Fachzeitschriften

Towards early diagnosis and treatment to save children from catastrophic epilepsy -- focus on epilepsy surgery.
Holthausen, H; Pieper, T; Kudernatsch, M;
Brain Dev. 2013; 35(8):730-741
Übersichtsarbeiten

2012

Beiträge in Fachzeitschriften

Neuropathologic measurements in focal cortical dysplasias: validation of the ILAE 2011 classification system and diagnostic implications for MRI.
Mühlebner, A; Coras, R; Kobow, K; Feucht, M; Czech, T; Stefan, H; Weigel, D; Buchfelder, M; Holthausen, H; Pieper, T; Kudernatsch, M; Blümcke, I;
Acta Neuropathol. 2012; 123(2):259-272
Originalarbeiten (Zeitschrift)
Predicting hand function after hemispherotomy: TMS versus fMRI in hemispheric polymicrogyria.
Zsoter, A; Pieper, T; Kudernatsch, M; Staudt, M;
Epilepsia. 2012; 53(6):e98-101
Originalarbeiten (Zeitschrift)

2010

Beiträge in Fachzeitschriften

A distinct variant of focal cortical dysplasia type I characterised by magnetic resonance imaging and neuropathological examination in children with severe epilepsies.
Blümcke, I; Pieper, T; Pauli, E; Hildebrandt, M; Kudernatsch, M; Winkler, P; Karlmeier, A; Holthausen, H;
Epileptic Disord. 2010; 12(3):172-180
Originalarbeiten (Zeitschrift)
Sustainability of motor performance after robotic-assisted treadmill therapy in children: an open, non-randomized baseline-treatment study.
Borggraefe, I; Kiwull, L; Schaefer, JS; Koerte, I; Blaschek, A; Meyer-Heim, A; Heinen, F;
Eur J Phys Rehabil Med. 2010; 46(2):125-131
Originalarbeiten (Zeitschrift)

2009

Beiträge in Fachzeitschriften

St. Valentine-patron saint of epilepsy: Illustrating the semiology of seizures over the course of six centuries
Kluger, G; Kudernatsch, V
EPILEPSY BEHAV. 2009; 14(1): 219-225.
Originalarbeiten (Zeitschrift)