' '
Deutsch | English    

Forschungsdatenbank PMU-SQQUID

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

PUBLIKATIONEN | Mitarbeiter/innen

39 Publikationen

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)
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)
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)
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)

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

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)
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)
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)
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): 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

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)