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Forschungsdatenbank PMU-SQQUID

VON STÜLPNAGEL-STEINBEIS CELINA
Universitätsklinik für Kinder- und Jugendheilkunde
Universitätsinstitut für Rehabilitation, Transition und Palliation von neurologisch kranken Kindern

Publikationen

28 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)
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)

2018

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)

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)
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)

2016

Beiträge in Fachzeitschriften

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)
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)
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

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

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)
Epilepsy in Aicardi-Goutières syndrome.
Ramantani, G; Maillard, LG; Bast, T; Husain, RA; Niggemann, P; Kohlhase, J; Hertzberg, C; Ungerath, K; Innes, MA; Walkenhorst, H; Bevot, A; von Stülpnagel, C; Thomas, K; Niemann, F; Ergun, MA; Tacke, U; Häusler, M; Ikonomidou, C; Korinthenberg, R; Lee-Kirsch, MA;
Eur J Paediatr Neurol. 2014; 18(1): 30-37.
Originalarbeiten (Zeitschrift)

2013

Beiträge in Fachzeitschriften

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

2012

Beiträge in Fachzeitschriften

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

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)
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)
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

2010

Beiträge in Fachzeitschriften

Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.
Ramantani, G; Kohlhase, J; Hertzberg, C; Innes, AM; Engel, K; Hunger, S; Borozdin, W; Mah, JK; Ungerath, K; Walkenhorst, H; Richardt, HH; Buckard, J; Bevot, A; Siegel, C; von Stülpnagel, C; Ikonomidou, C; Thomas, K; Proud, V; Niemann, F; Wieczorek, D; Häusler, M; Niggemann, P; Baltaci, V; Conrad, K; Lebon, P; Lee-Kirsch, MA;
Arthritis Rheum. 2010; 62(5): 1469-1477.
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

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
Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option.
von Stülpnagel, C; Reilich, P; Straube, A; Schäfer, J; Blaschek, A; Lee, SH; Müller-Felber, W; Henschel, V; Mansmann, U; Heinen, F;
J Child Neurol. 2009; 24(4): 406-409.
Originalarbeiten (Zeitschrift)

2007

Beiträge in Fachzeitschriften

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)

2006

Beiträge in Fachzeitschriften

Migraine therapy in childhood. Update
Lee, SH; von Stulpnagel, C; Heinen, F
MONATSSCHR KINDERH. 2006; 154(8): 764-+.
Originalarbeiten (Zeitschrift)
[Primary headache in children].
Von Stülpnagel, C; Blaschek, A; Lee, SH; Heinen, F;
MMW Fortschr Med. 2006; 148(46): 39-41.
Originalarbeiten (Zeitschrift)

2001

Beiträge in Fachzeitschriften

Association of myocardial infarction with mononuclear cell expression of the cytomegalovirus chemokine receptor US28 in patients with NIDDM.
Weber, C; von Stülpnagel, C; Weber, KS; Hengel, H; Weber, PC;
Exp Clin Cardiol. 2001; 6(2): 105-108.
Originalarbeiten (Zeitschrift)