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Forschungsdatenbank PMU-SQQUID

KLUGER GERHARD
Universitätsklinik für Kinder- und Jugendheilkunde
Universitätsinstitut für Rehabilitation, Transition und Palliation von neurologisch kranken Kindern

Publikationen | Forscherprofil

98 Publikationen

2019

Beiträge in Fachzeitschriften

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)
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 Neurol. 2019; 6(4):655-668
Originalarbeiten (Zeitschrift)
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.
Stülpnagel, CV; 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; 65:131-137
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):267-272
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)

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
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)
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)
Benign epilepsy with centrotemporal spikes: Correlating spike frequency and neuropsychology.
Tacke, M; Rupp, N; Gerstl, L; Heinen, F; Vill, K; Bonfert, M; Neubauer, BA; Bast, T; Borggraefe, I;
Acta Neurol Scand. 2018; 138(6): 475-481.
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): e2078-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)

2017

Beiträge in Fachzeitschriften

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)
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)
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)
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)
Epilepsy caused by PCDH19 gene mutation: a review of literature and the authors’ observations
Mukhin, KY; Pylaeva, OA; Dolinina, AF; Moiseeva, S; Verbitskaya, YV; Petrukhin, AS; Kluger, G; Holthausen, H; Staudt, M;
Russian journal of child neurology. 2016; 11(2): 26-32.
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)
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region.
Nicita, F; Garone, G; Spalice, A; Savasta, S; Striano, P; Pantaleoni, C; Spartà, MV; Kluger, G; Capovilla, G; Pruna, D; Freri, E; D"Arrigo, S; Verrotti, A;
Am J Med Genet A. 2016; 170(1):148-155
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)
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)
The phenotypic spectrum of SCN8A encephalopathy.
Larsen, J; Carvill, GL; Gardella, E; Kluger, G; Schmiedel, G; Barisic, N; Depienne, C; Brilstra, E; Mang, Y; Nielsen, JE; Kirkpatrick, M; Goudie, D; Goldman, R; Jähn, JA; Jepsen, B; Gill, D; Döcker, M; Biskup, S; McMahon, JM; Koeleman, B; Harris, M; Braun, K; de Kovel, CG; Marini, C; Specchio, N; Djémié, T; Weckhuysen, S; Tommerup, N; Troncoso, M; Troncoso, L; Bevot, A; Wolff, M; Hjalgrim, H; Guerrini, R; Scheffer, IE; Mefford, HC; Møller, RS;
Neurology. 2015; 84(5): 480-489.
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): 368-378.
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; Kudematsch, 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

Co-occurring malformations of cortical development and SCN1A gene mutations.
Barba, C; Parrini, E; Coras, R; Galuppi, A; Craiu, D; Kluger, G; Parmeggiani, A; Pieper, T; Schmitt-Mechelke, T; Striano, P; Giordano, F; Blumcke, I; Guerrini, R;
Epilepsia. 2014; 55(7): 1009-1019.
Originalarbeiten (Zeitschrift)
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)
Current role of rufinamide in the treatment of childhood epilepsy: Literature review and treatment guidelines.
Coppola, G; Besag, F; Cusmai, R; Dulac, O; Kluger, G; Moavero, R; Nabbout, R; Nikanorova, M; Pisani, F; Verrotti, A; von Stülpnagel, C; Curatolo, P;
Eur J Paediatr Neurol. 2014; 18(6):685-690
Originalarbeiten (Zeitschrift)
German translation of the caregiver priorities and child health index of life with disabilities questionnaire: test-retest reliability and correlation with gross motor function in children with cerebral palsy.
Jung, NH; Brix, O; Bernius, P; Schroeder, AS; Kluger, GJ; Beyerlein, A; Weir, S; von Kries, R; Narayanan, UG; Mall, V; Berweck, S;
Neuropediatrics. 2014; 45(5):289-293
Originalarbeiten (Zeitschrift)
Does hip displacement influence health-related quality of life in children with cerebral palsy?
Jung, NH; Pereira, B; Nehring, I; Brix, O; Bernius, P; Schroeder, SA; Kluger, GJ; Koehler, T; Beyerlein, A; Weir, S; von Kries, R; Narayanan, UG; Berweck, S; Mall, V;
Dev Neurorehabil. 2014; 17(6):420-425
Originalarbeiten (Zeitschrift)
DEPDC5 mutations in genetic focal epilepsies of childhood.
Lal, D; Reinthaler, EM; Schubert, J; Muhle, H; Riesch, E; Kluger, G; Jabbari, K; Kawalia, A; Bäumel, C; Holthausen, H; Hahn, A; Feucht, M; Neophytou, B; Haberlandt, E; Becker, F; Altmüller, J; Thiele, H; Lemke, JR; Lerche, H; Nürnberg, P; Sander, T; Weber, Y; Zimprich, F; Neubauer, BA;
Ann Neurol. 2014; 75(5): 788-792.
Originalarbeiten (Zeitschrift)

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

Rufinamide for refractory focal seizures: an open-label, multicenter European study.
Coppola, G; Zamponi, N; Kluger, G; Mueller, A; Anna Rita, M; Parisi, P; Isone, C; Santoro, E; Curatolo, P; Verrotti, A;
Seizure. 2013; 22(1): 33-36.
Originalarbeiten (Zeitschrift)
Advancing the management of childhood epilepsies
Cross, JH; Kluger, G; Lagae, L
EUR J PAEDIATR NEURO. 2013; 17(4): 334-347.
Übersichtsarbeiten
Generalized Epilepsy in Two Patients with 5p Duplication
Kluger, G; Koehler, U; Neuhann, TM; Pieper, T; Staudt, M; von Stulpnagel, C
NEUROPEDIATRICS. 2013; 44(4): 225-229.
Fallberichte
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; 45(9): 106-172.
Originalarbeiten (Zeitschrift)
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome.
Suls, A; Jaehn, JA; Kecskés, A; Weber, Y; Weckhuysen, S; Craiu, DC; Siekierska, A; Djémié, T; Afrikanova, T; Gormley, P; von Spiczak, S; Kluger, G; Iliescu, CM; Talvik, T; Talvik, I; Meral, C; Caglayan, HS; Giraldez, BG; Serratosa, J; Lemke, JR; Hoffman-Zacharska, D; Szczepanik, E; Barisic, N; Komarek, V; Hjalgrim, H; Møller, RS; Linnankivi, T; Dimova, P; Striano, P; Zara, F; Marini, C; Guerrini, R; Depienne, C; Baulac, S; Kuhlenbäumer, G; Crawford, AD; Lehesjoki, AE; de Witte, PA; Palotie, A; Lerche, H; Esguerra, CV; De Jonghe, P; Helbig, I;
Am J Hum Genet. 2013; 93(5): 96-75.
Originalarbeiten (Zeitschrift)
Lacosamide in pediatric and adult patients: comparison of efficacy and safety.
Verrotti, A; Loiacono, G; Pizzolorusso, A; Parisi, P; Bruni, O; Luchetti, A; Zamponi, N; Cappanera, S; Grosso, S; Kluger, G; Janello, C; Franzoni, E; Elia, M; Spalice, A; Coppola, G; Striano, P; Pavone, P; Savasta, S; Viri, M; Romeo, A; Aloisi, P; Gobbi, G; Ferretti, A; Cusmai, R; Curatolo, P;
Seizure. 2013; 22(3): 210-216.
Originalarbeiten (Zeitschrift)

2012

Beiträge in Fachzeitschriften

Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations
Appenzeller, S; Helbig, I; Stephani, U; Hausler, M; Kluger, G; Bungeroth, M; Muller, S; Kuhlenbaumer, G; Van Baalen, A
DEV MED CHILD NEUROL. 2012; 54(12): 1144-1148.
Originalarbeiten (Zeitschrift)
Bromide in patients with SCN1A-mutations manifesting as Dravet syndrome.
Lotte, J; Haberlandt, E; Neubauer, B; Staudt, M; Kluger, GJ;
NEUROPEDIATRICS. 2012; 43(1): 17-21.
Originalarbeiten (Zeitschrift)
Delineation and Diagnostic Criteria of Oral-Facial-Digital Syndrome Type VI
Poretti, A; Vitiello, G; Hennekam, RCM; Arrigoni, F; Bertini, E; Borgatti, R; Brancati, F; DxxxArrigo, S; Faravelli, F; Giordano, L; Huisman, TAGM; Iannicelli, M; Kluger, G; Kyllerman, M; Landgren, M; Lees, MM; Pinelli, L; Romaniello, R; Scheer, I; Schwarz, CE; Spiegel, R; Tibussek, D; Valente, EM; Boltshauser, E
ORPHANET J RARE DIS. 2012; 7: 4
Originalarbeiten (Zeitschrift)
Febrile Infection-Related Epilepsy Syndrome without Detectable Autoantibodies and Response to Immunotherapy: A Case Series and Discussion of Epileptogenesis in FIRES
van Baalen, A; Hausler, M; Plecko-Startinig, B; Strautmanis, J; Vlaho, S; Gebhardt, B; Rohr, A; Abicht, A; Kluger, G; Stephani, U; Probst, C; Vincent, A; Bien, CG
NEUROPEDIATRICS. 2012; 43(4): 209-216.
Originalarbeiten (Zeitschrift)
First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome).
von Stülpnagel, C; Coppola, G; Striano, P; Müller, A; Staudt, M; Kluger, G;
EUR J PAEDIATR NEURO. 2012; 16(5): 459-463.
Originalarbeiten (Zeitschrift)

2011

Beiträge in Fachzeitschriften

Limbic encephalitis in children and adolescents
Haberlandt, E; Bast, T; Ebner, A; Holthausen, H; Kluger, G; Kravljanac, R; Kroll-Seger, J; Kurlemann, G; Makowski, C; Rostasy, K; Tuschen-Hofstatter, E; Weber, G; Vincent, A; Bien, CG
ARCH DIS CHILD. 2011; 96(2): 186-191.
Originalarbeiten (Zeitschrift)
Epilepsy with myoclonic absences - favourable response to add-on rufinamide treatment in 3 cases.
Häusler, M; Kluger, G; Nikanorova, M;
Neuropediatrics. 2011; 42(1): 28-29.
Fallberichte
Evolution and management of Lennox-Gastaut syndrome through adolescence and into adulthood: are seizures always the primary issue?
Kerr, M; Kluger, G; Philip, S
EPILEPTIC DISORD. 2011; 13: S15-S26.
Übersichtsarbeiten
The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis
Kortum, F; Das, S; Flindt, M; Morris-Rosendahl, DJ; Stefanova, I; Goldstein, A; Horn, D; Klopocki, E; Kluger, G; Martin, P; Rauch, A; Roumer, A; Saitta, S; Walsh, LE; Wieczorek, D; Uyanik, G; Kutsche, K; Dobyns, WB
J MED GENET. 2011; 48(6): 396-406.
Originalarbeiten (Zeitschrift)
Febrile infection-related epilepsy syndrome (FIRES): Does duration of anesthesia affect outcome?
Kramer, U; Chi, CS; Lin, KL; Specchio, N; Sahin, M; Olson, H; Kluger, G; van Baalen, A
EPILEPSIA. 2011; 52: 28-30.
Originalarbeiten (Zeitschrift)
Febrile infection-related epilepsy syndrome (FIRES): Pathogenesis, treatment, and outcome A multicenter study on 77 children
Kramer, U; Chi, CS; Lin, KL; Specchio, N; Sahin, M; Olson, H; Nabbout, R; Kluger, G; Lin, JJ; van Baalen, A
EPILEPSIA. 2011; 52(11): 1956-1965.
Originalarbeiten (Zeitschrift)
Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome
Mueller, A; Boor, R; Coppola, G; Striano, P; Dahlin, M; von Stuelpnagel, C; Lotte, J; Staudt, M; Kluger, G
EPILEPSY BEHAV. 2011; 21(3): 282-284.
Originalarbeiten (Zeitschrift)
Rufinamide from clinical trials to clinical practice in the United States and Europe
Resnick, T; Arzimanoglou, A; Brown, LW; Flamini, R; Kerr, M; Kluger, G; Kothare, S; Philip, S; Harrison, M; Narurkar, M
EPILEPTIC DISORD. 2011; 13: S27-S43.
Übersichtsarbeiten
A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome
Tro-Baumann, B; von Spiczak, S; Lotte, J; Bast, T; Haberlandt, E; Sassen, R; Freund, A; Leiz, S; Stephani, U; Boor, R; Holthausen, H; Helbig, I; Kluger, G
EPILEPSIA. 2011; 52(1): 175-178.
Originalarbeiten (Zeitschrift)
Impact of ABCC2 genotype on antiepileptic drug response in Caucasian patients with childhood epilepsy
Ufer, M; von Stulpnagel, C; Muhle, H; Haenisch, S; Remmler, C; Majed, A; Plischke, H; Stephani, U; Kluger, G; Cascorbi, I
PHARMACOGENET GENOM. 2011; 21(10): 624-630.
Originalarbeiten (Zeitschrift)
Treatment of malignant migrating partial epilepsy of infancy with rufinamide: report of five cases
Vendrame, M; Poduri, A; Loddenkemper, T; Kluger, G; Coppola, G; Kothare, SV
EPILEPTIC DISORD. 2011; 13(1): 18-21.
Fallberichte
Refractory Focal Epilepsy in a Patient with Methylmalonic Aciduria: Case Report on Positive and Long-lasting Effect of Rufinamide
von Stulpnagel, C; Leichsenring, M; Muller, A; Staudt, M; Kluger, G
NEUROPEDIATRICS. 2011; 42(2): 71-73.
Fallberichte
Neurological early rehabilitation in children and adolescents
Zsoter, A; Berweck, S; Kluger, G; Staudt, M
MONATSSCHR KINDERH. 2011; 159(7): 634-641.
Originalarbeiten (Zeitschrift)

2010

Beiträge in Fachzeitschriften

News from the pharmacotherapy: lacosamide, eslicarbazepinacetate, rufinamide, stiripentol
Arnold, S; Kluger, G
NERVENHEILKUNDE. 2010; 29(4): 191-198.
Originalarbeiten (Zeitschrift)
Adjunctive rufinamide in Lennox-Gastaut syndrome: a long-term, open-label extension study
Kluger, G; Glauser, T; Krauss, G; Seeruthun, R; Perdomo, C; Arroyo, S
ACTA NEUROL SCAND. 2010; 122(3): 202-208.
Originalarbeiten (Zeitschrift)
First European long-term experience with the orphan drug rufinamide in childhood-onset refractory epilepsy
Kluger, G; Haberlandt, E; Kurlemann, G; Ernst, JP; Runge, U; Schneider, F; Makowski, C; Boor, R; Bast, T
EPILEPSY BEHAV. 2010; 17(4): 546-548.
Originalarbeiten (Zeitschrift)
Febrile infection-related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood
van Baalen, A; Hausler, M; Boor, R; Rohr, A; Sperner, J; Kurlemann, G; Panzer, A; Stephani, U; Kluger, G
EPILEPSIA. 2010; 51(7): 1323-1328.
Originalarbeiten (Zeitschrift)
Levetiracetam as add-on therapy in different subgroups of "benign" idiopathic focal epilepsies in childhood
von Stulpnagel, C; Kluger, G; Leiz, S; Holthausen, H
EPILEPSY BEHAV. 2010; 17(2): 193-198.
Originalarbeiten (Zeitschrift)

2009

Beiträge in Fachzeitschriften

Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology
Arzimanoglou, A; French, J; Blume, WT; Cross, JH; Ernst, JP; Feucht, M; Genton, P; Guerrini, R; Kluger, G; Pellock, JM; Perucca, E; Wheless, JW
LANCET NEUROL. 2009; 8(1): 82-93.
Übersichtsarbeiten
Changes in elementary finger-hand functions over time in preschool children with spastic cerebral palsy
Blank, R; Kluger, G
NEUROSCI LETT. 2009; 455(1): 30-35.
Originalarbeiten (Zeitschrift)
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)
Effectiveness and tolerability of rufinamide in children and adults with refractory epilepsy: First European experience
Kluger, G; Kurlemann, G; Haberlandt, E; Ernst, JP; Runge, U; Schneider, F; Makowski, C; Boor, R; Bast, T
EPILEPSY BEHAV. 2009; 14(3): 491-495.
Originalarbeiten (Zeitschrift)
Effectiveness of Low Dose of Topiramate Following Rapid Titration in Multiply Handicapped Children and Difficult-to-Treat Epilepsy
Kluger, G; Schauble, B; Rettig, K; Schreiner, A; Holthausen, H
NEUROPEDIATRICS. 2009; 40(2): 61-65.
Originalarbeiten (Zeitschrift)
FIRES: febrile infection responsive epileptic (FIRE) encephalopathies of school age.
van Baalen, A; Stephani, U; Kluger, G; Häusler, M; Dulac, O;
Brain Dev. 2009; 31(1): 91; author reply 92-3
Letter
Letter: Lack of association between MDR1 polymorphisms and pharmacoresistance to anticonvulsive drugs in patients with childhood-onset epilepsy
von Stulpnagel, C; Plischke, H; Zill, P; Baumel, C; Spiegel, R; Gruber, R; Kluger, G
EPILEPSIA. 2009; 50(7): 1835-1837.
Letter

2008

Beiträge in Fachzeitschriften

Rufinamide for generalized seizures associated with Lennox-Gastaut syndrome.
Glauser, T; Kluger, G; Sachdeo, R; Krauss, G; Perdomo, C; Arroyo, S;
Neurology. 2008; 70(21): 1950-1958.
Originalarbeiten (Zeitschrift)
Pyridoxine-dependent Epilepsy: Normal Outcome in a Patient with Late Diagnosis after Prolonged Status Epilepticus Causing Cortical Blindness
Kluger, G; Blank, R; Paul, K; Paschke, E; Jansen, E; Jakobs, C; Worle, H; Plecko, B
NEUROPEDIATRICS. 2008; 39(5): 276-279.
Fallberichte
Long-term use of zonisamide in refractory childhood-onset epilepsy.
Kluger, G; Zsoter, A; Holthausen, H;
Eur J Paediatr Neurol. 2008; 12(1): 19-23.
Originalarbeiten (Zeitschrift)
Electroencephalographic evolution of hypsarrhythmia: Toward an early treatment option
Philippi, H; Wohlrab, G; Bettendorf, U; Borusiak, P; Kluger, G; Strobl, K; Bast, T
EPILEPSIA. 2008; 49(11): 1859-1864.
Originalarbeiten (Zeitschrift)

2007

Beiträge in Fachzeitschriften

Seizures, psychosis and coma: severe course of hashimoto encephalopathy in a six-year-old girl.
Hoffmann, F; Reiter, K; Kluger, G; Holthausen, H; Schwarz, HP; Borggraefe, I; Bonfig, W;
Neuropediatrics. 2007; 38(4): 197-199.
Fallberichte
Role of rufinamide in the management of Lennox-Gastaut syndrome (childhood epileptic encephalopathy).
Kluger, G; Bauer, B;
Neuropsychiatr Dis Treat. 2007; 3(1): 3-11.
Originalarbeiten (Zeitschrift)
Long-term use of Levetiracetam in patients with severe childhood-onset epilepsy.
von Stuelpnagel, C; Holthausen, H; Kluger, G;
Eur J Paediatr Neurol. 2007; 11(6): 341-345.
Originalarbeiten (Zeitschrift)
famoses: A modular educational program for children with epilepsy and their parents
Wohlrab, GC; Rinnert, S; Bettendorf, U; Fischbach, H; Heinen, G; Klein, P; Kluger, G; Jacob, K; Rahn, D; Winter, R; Pfafflin, M
EPILEPSY BEHAV. 2007; 10(1): 44-48.
Originalarbeiten (Zeitschrift)

2006

Beiträge in Fachzeitschriften

Valproic acid-induced hepatopathy: nine new fatalities in Germany from 1994 to 2003.
Koenig, SA; Buesing, D; Longin, E; Oehring, R; Häussermann, P; Kluger, G; Lindmayer, F; Hanusch, R; Degen, I; Kuhn, H; Samii, K; Jungck, A; Brückner, R; Seitz, R; Boxtermann, W; Weber, Y; Knapp, R; Richard, HH; Weidner, B; Kasper, JM; Haensch, CA; Fitzek, S; Hartmann, M; Borusiak, P; Müller-Deile, A; Degenhardt, V; Korenke, GC; Hoppen, T; Specht, U; Gerstner, T;
Epilepsia. 2006; 47(12): 2027-2031.
Originalarbeiten (Zeitschrift)

2005

Beiträge in Fachzeitschriften

Levetiracetam in children with refractory epilepsy: A multicenter open label study in Germany
Opp, J; Tuxhorn, I; May, T; Kluger, G; Wiemer-Kruel, A; Kurlemann, G; Gross-Selbeck, G; Rating, D; Brandl, U; Bettendorf, U; Hartel, C; Korn-Merker, E
SEIZURE-EUR J EPILEP. 2005; 14(7): 476-484.
Originalarbeiten (Zeitschrift)

2001

Beiträge in Fachzeitschriften

The long-term use of vigabatrin and lamotrigine in patients with severe childhood onset epilepsy.
Kluger, G; Berz, K; Holthausen, H;
Eur J Paediatr Neurol. 2001; 5(1): 37-40.
Originalarbeiten (Zeitschrift)
Lack of association between childhood stroke after varicella and human leukocyte antigen (HLA)-B51.
Kluger, G; Hubmann, M; Vogler, L; Berz, K;
Eur J Paediatr Neurol. 2001; 5(6): 259-260.
Originalarbeiten (Zeitschrift)

2000

Beiträge in Fachzeitschriften

Heterotopic ossification in childhood and adolescence
Kluger, G; Kochs, A; Holthausen, H
J CHILD NEUROL. 2000; 15(6): 406-413.
Originalarbeiten (Zeitschrift)

1996

Beiträge in Fachzeitschriften

Epilepsy and fragile X gene mutations
Kluger, G; Bohm, I; Laub, MC; Waldenmaier, C
PEDIATR NEUROL. 1996; 15(4): 358-360.
Fallberichte

1995

Beiträge in Fachzeitschriften

TICKBORNE ENCEPHALITIS DESPITE SPECIFIC IMMUNOGLOBULIN PROPHYLAXIS
KLUGER, G; SCHOTTLER, A; WALDVOGEL, K; NADAL, D; HINRICHS, W; WUNDISCH, GF; LAUB, MC
LANCET. 1995; 346(8988): 1502-1502.
Letter

1984

Beiträge in Fachzeitschriften

Uremic pneumonitis. Evidence for participation of proteolytic enzymes.
Heidland, A; Heine, H; Heidbreder, E; Haunschild, J; Weipert, J; Gilge, U; Kluger, G; Hörl, WH;
Contrib Nephrol. 1984; 41: 352-366.
Originalarbeiten (Zeitschrift)