DOI : 10.1055/s-00000041

Neuropediatrics

Issue S 01 · Volume 47 · April 2016 DOI: 10.1055/s-006-31610


Abstracts of the 42nd Annual Meeting of the Society for Neuropediatrics
Bochum, 21–24 April 2016

Chair: Prof. Dr. med. Ulrike Schara, Department of Neuropediatrics, Developmental Medicine and Social Pediatrics, University Children's Hospital Essen, University Duisburg-Essen, Essen, Germany; Co-Chair: Prof. Dr. med. Thomas Lüke, Department of Neuropediatrics, University Children's Hospital, Ruhr-University Bochum, Bochum, Germany
Abstracts (HTML) List of Authors
P01-01
Maier, O.; König, N.; Künzle, C.; Wirth-Barben, G.; Courage, C.; Hörtnagel, K.; Lemke, J.: West Syndrome, Severe Developmental Retardation, and Intermittent Horizontal Saccade Failure: An Expanded Spectrum of STXBP1-Epileptic Encephalopathy
P01-02
Tibussek, D.; Pfahl, S.; Höhn, T.; Sabir, H.: Neonatal Seizures and Response to Phenobarbitone: A Three-Year Single-Center Experience
P01-03
Berthold, O.; Nestler, M.; von Moers, A.; Panzer, A.: Hypocalcemic Partial Seizures in the Newborn
P01-04
Goldhahn, K.; Polster, T.; von Moers, A.; Panzer, A.: Hemispherectomy in Familial Focal Epilepsy? A Case Report of a Pharmacoresistant Epilepsy with Malformation of Cortical Development
P01-05
Lange, J.; Pieper, T.; Hartlieb, T.; Winkler, P.; Kudernatsch, M.; Staudt, M.: How Red Are Red Flags in Lesional Childhood Temporal Lobe Epilepsy? An Electro-Clinico-Anatomical Correlation Analysis of Intracranial Video-EEG Data
P01-06
Pechmann, A.; Wellmann, S.; Krüger, M.; Zieger, B.: Increased Levels of von Willebrand Factor Parameters in Children with Febrile Seizures
P01-07
von Stülpnagel-Steinbeis, C.; Betzler, C.; Kluger, G.: Study Group: Personalized Therapy in Rare Pediatric Epilepsies
P01-08
Thiels, Ch.; Hoffjan, S.; Köhler, C.; Lücke, T.: Duplication within the KCNQ2 Gene in a Child with Benign Early-Onset Epileptic Encephalopathy
P01-09
Neumann, H.; Helmke, F.; Thiels, Ch.; Köhler, C.; Selzer, L.; Daseking, M.; Petermann, F.; Lücke, T.: Cognitive Development in Children with Rolandic EEG Pattern: First Results of a Prospective Follow-Up Study
P01-11
Polster, T.; Kalbhenn, T.; Korenke, C.; Cloppenborg, T.; Herting, A.; Woermann, F. G.: Seizures after Hemispherectomy: The Role of the Insula
P01-12
Hofmeister, B.; Berweck, S.; Betzler, C.; Christen, H. J.; Grunt, S.; Haberlandt, E.; Haeckl, B.; Herberhold, T.; Jansen, K.; Kluger, G.; Moiseeva, S.; Schilling, S.; von Stülpnagel-Steinbeis, C.; Weber, P.: Epilepsy and Its Treatment in Nicolaides-Baraitser and Coffin-Siris Syndromes
P01-13
Leiz, S.; Petrova, S.; Ahting, U.; Alhaddad, B.; Baethmann, M.; Freisinger, P.; Haack, T. B.: Compound Heterozygous COQ4 Missense Mutations Cause Coenzyme Q10 Deficiency Associated with Severe Infantile Epileptic Encephalopathy and Cerebellar Cysts
P01-14
Lampert, A.; Hoffmann, G. F.; Ries, M.: Ten Years after the International Committee of Medical Journal Editors’ Clinical Trial Registration Initiative, One Quarter of Phase 3 Pediatric Epilepsy Clinical Trials Still Remain Unpublished: A Cross-Sectional Analysis
P01-15
Panzer, A.; Thorpe, Bione S.: CDKL 5 Mutation: The Viewpoint of Self-Help Organization
P01-16
Neu, A.; Bast, T.; Dietel, T.; Leiz, S.; Wolff, M.; Ruf, S.; Schubert-Bast, S.; Denecke, J.; Hornig, S.; Fazeli, W.; Gellermann, J.; Bähring, R.: In Vitro Characterization of KCNT1 Mutations from Pediatric Patients
P01-17
Dietel, T.; Haack, T. B.; Schlüter, G.; Cordes, I.; Trollmann, R.; Bast, T.: Genotype and phenotype in GNAO1-Mutation – Case report of an unusual course of a childhood epilepsy
P01-18
Wildbolz, M.; Strozzi, S.; Kohler, B.; Pfammatter, J. P.; Pallivathukal, S.; Perret-Hoigné, E.; Schindler, K.; Noti, F.; Bigi, S.: Prolonged Postictal Asystole in a Child with Focal Epilepsy and Cerebellar Atrophy
P01-19
Zellner, H.; Baumann, M.; Zotter, S.; Albrecht, U.; Baumgartner, Sigl S.; Gedik, A.; Zeiner, F.; Egger, S.; Heinz-Erian, E.; Kössler, M.; Lechner, C.; Zschocke, A.; Haberlandt, E.: Landau-Kleffner Syndrome (Epileptic Aphasia)
P01-20
Finetti, C.; Gerling, Ch.; Schlump, J-U.; Utz, N.; Schweiger, T.: Reversible cMRI Changes After Status Epilepticus: Two Case Reports And a Review
P02-01
Losch, H.; Viemann, M.; Kowald, T.; Korenke, G. C.: Neonatal Moyamoya Disease of Unclear Origin
P02-02
Henzi, B.; Grunt, S.; Wagner, B.; Verma, R.; Vulcu, S.; Bigi, S.: Perinatal Infratentorial Hemorrhage: A Rare but Possibly Life-Threatening Condition
P02-04
Kößler, M.; Baumann, M.; Zellner, H.; Heinz-Erian, E.; Egger, S.; Lechner, C.; Baumgartner, S.; Albrecht, U.; Zeiner, F.; Rostasy, K.; Haberlandt, E.: Overview of Headache in Children and Adolescents in an Outpatient Neuropediatric Center from 2014 to 2015
P02-06
Wernicke, C. M.; Balling, G.; Makowski, C.; Beutel, K.; Pringsheim, M.; Staudt, M.; Mall, V.; Juenger, H.: Thrombolysis in Pediatric Arterial Ischemic Stroke: Report of Two Young Children
P02-07
Braun, S.; Marquard, K.; Schroth, M.; Wörle, H.; Eckenweiler, M.; Korinthenberg, R.; Blankenburg, M.: Cluster Headache in Childhood and Adolescence: Two Case Reports
P02-08
Kruker, A. T.; Bauder, F.; Kaiser, D.; Schmitt-Mechelke, T.: Two Cases of an Unusual Cause of Headache and Papilledema not to be Missed
P02-09
Burkhardt, L.; Lobitz, S.; Koustenis, E.; Rueckriegel, S. M.; Hernáiz, Driever P.: Cognitive and Fine Motor Deficits in a Pediatric Sickle Cell Disease Cohort of Mainly Middle Eastern Origin
P03-01
Spönemann, N.; Della, Marina A.; Dohna-Schwake, C.; Möller-Hartmann, C.; Keyvani, K.; Florian, M.; Lutz, S.; Hoyer, P. F.; Schara, U.: Acute Hemorrhagic Leukoencephalitis with Proof of Activation of the Complement System and Eculizumab Therapy
P03-02
Antenbrink, F.; Sandrieser, T.; Hoppen, T.; Lorey, M.; Nüßlein, T.: Rotavirus Encephalitis Resulting in Severe Impairment in a Toddler
P03-04
Scheffner, T.; Schell, C.; Dütting, T.; Jaggy, L.; Grimm, J.; Freisinger, P.: Simultaneous Occurrence of Myelitis and Guillain-Barré Syndrome (GBS) Caused by Mycoplasma Pneumoniae with Positive Outcome
P03-06
Lischetzki, G.; Ungerath, K.; Heinemeyer, J.: Meningitis Caused by Listeria Monocytogenes during Methylprednisolone Pulse Therapy
P03-07
Schneider, R.; Deutz, U.; Schoberer, A.; Trepels-Kottek, S.; Schoberer, M.; Orlikowsky, Th.; Neuloh, G.; Häusler, M.: Case Reports: Intracranial Abscesses
P03-08
Vogl, M.; Della, Marina A.; Möller-Hartmann, C.; Stehling, F.: Tuberculosis Meningitis with Brainstem Mass Lesion—Adjunctive Treatment with Thalidomide: A Case Report
P03-11
Salamano, E.; Freisinger, P.; Mayr, J.; Hack, T.; Weissbrich, B.; Klepper, J.; Moser, K.; Heußinger, N.: Acute Necrotizing Encephalopathy of Childhood Associated with Primary Infection of HHV 6: An Important Differential Diagnosis of Mitochondrial Diseases
P03-12
Greulich, N.; Klepper, J.; Heußinger, N.: Enterovirus Induced Opsoclonus-Myoclonus Syndrome in a 16-Month-Old Girl
P03-15
Kraus, V.; Makowski, C.; Jünger, H.; Wawer, A.; Strotmann, P.; Mall, V.; Strotmann, P.; Burdach, S.: Longitudinal Extensive Transverse Myelitis following T-ALL
P03-16
Stöhr, K.; Herberhold, T. M.; Niedermeyer, H. P.; Staudt, M.: Cochlear Edema and Sclerosis following Meningitis by S. Pneumoniae: Only Early Audiometry Allows Optimal Cochlear Implantation (CI)
P03-18
Schuler, E.; Ziegler, A.; Kaiser, A.-S.; Doering, J.-H.; Hoffmann, G. F.; Brösse, I.: Enterovirus-Associated Brain Stem Encephalitis Mistaken for Epilepsia Partialis Continua
P04-01
Brand, L.; Preuße, C.; van Moers, A.; Kölbel, H.; Stenzel, W.; Schara, U.: Analysis of the Specific Immune Response in Skeletal Muscle in LGMD2I Patients
P04-02
Schara, U.; McDonald, C. M.; Bushby, K.; Tulinius, M.; Finkel, R.; Topaloglu, H.; Day, J. W.; Flanigan, K.; Lowes, L.; Eagle, M.; Luo, X.; Elfring, G.; Kroger, H.; Riebling, P.; Ong, T.; Spiegel, R.; Peltz, S. W.; Park, S.-M.: Ataluren: Clinical Trial Results in Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD)
P04-03
Park, S.-M.; McDonald, C. M.; Sweeney, H. L.; Luo, X.; Elfring, G.; Kroger, H.; Riebling, P.; Ong, T.; Spiegel, R.; Peltz, S. W.; Mercuri, E.; Schara, U.: The Six-Minute Walk Test (6MWT) as Endpoint in Duchenne Muscular Dystrophy (DMD) Clinical Studies
P04-04
Gossler, A.; Klinge, L.; Kreß, W.; Wilichowski, E.: In-Frame Deletion in ISPD Gene Causes Limb Girdle Muscular Dystrophy: A Case Report
P04-06
Anastasopoulos, C.; Hooijmans, M.; Burakiewicz, J.; Webb, A.; Kirschner, J.; Verschuuren, J.; Niks, E.; Kan, H.: Increased Heterogeneity in T2-Relaxation Times in the Dystrophic Soleus Muscle
P04-07
Pross, I.; Braun, S.; Schroth, M.; Wörle, H.; Marquard, K.; von Kalle, T.; Blankenburg, M.: Idiopathic Carpal Tunnel Syndrome in Childhood: Two Case Reports
P04-08
Janisch, M.; Nolte-Buchholtz, S.; von der Hagen, M.: What Kind of General and Special Palliative Care Do Children, Adolescents, and Young Adults with Duchenne Muscular Dystrophy Need?
P04-09
Straßer, K.; Haack, T.; Ahting, U.; Dörr, H. G.; Trollmann, R.: Hypoparathyroidism, Cardiomyopathy, and Encephalomyopathy Caused by mt Depletion Syndrome due to a Novel Mutation in VARS2: A Case Report
P04-10
Giagkou, E.; Zuzak, T.; Schara, U.: Use of Complementary and Alternative Medicine (CAM) in Patients with X-Linked Recessive Duchenne Muscular Dystrophy (DMD)
P04-11
Dehmel, M.; Hu, H.; Hahn, G.; Wienker, T. F.; Musante, L.; Ropers, H. H.; Huebner, A.; Kaindl, A. M.; von der Hagen, M.: Congenital Muscular Dystrophy-Dystroglycanopathy (MDDGA1) in a Consanguineous Family with Compound Heterozygous Mutations of the POMT1 Gene and Variable Clinical Severity
P04-12
Borell, S.; Klemann, C.; Has, C.; Zieger, B.; Ehl, R. S.; Kirschner, J.: Tubular Aggregate Myopathy Caused by an Autosomal Dominant Mutation in ORAI 1 Gene
P04-13
Pfeifer, N.; Della, Marina A.; Kathemann, S.; Hegen, B.; Lutz, S.; Hoyer, P. F.; Schara, U.: Elevated Creatinine Kinase in Connection with Wilson Disease: Atypical Presentation with Musculoskeletal Symptoms or Associated Neuromuscular Disease
P04-14
Hobbiebrunken, E.; Stettner, G. M.; Hehr, U.; Hübner, A.; Wilichowski, E.: Homozygote Deletion of Fukutin Gene (FKTN) Exon 3 Causes Dilated Cardiomyopathy and Mild Limb-Girdle Muscular Dystrophy without Brain Involvement
P04-15
Mayer, V.; Bulst, S.; Nissen, A.; Kleinle, S.; Becker, K.; Walter, M. C.; Benet-Pagès, A.; Abicht, A.: Multi-Gene Panel Analysis in the Primary Diagnosis of Limb-Girdle Muscular Dystrophy
P04-16
Dieckmann, A.; Majer, F.; Hulkova, H.; Farr, M.; Kalina, T.; Romeike, B.; Vlaskova, H.; Brandl, U.; Sikora, J.; Husain, R. A.: Danon Disease: Clinical Presentation and Diagnostic Workup in a Case of a Male Patient with a Novel Mutation in the LAMP2 Gene
P04-17
Belke, F.; Augst, D.; Konrad, K.; Finetti, C.: Rhabdomyolysis as a Rare Complication of Diabetic Ketoacidosis in a Twelve-Year-Old Boy
P04-18
Wimmer, C.; Jansen, C.; Schroeder, A. S.; Berweck, S.: Muscle-Adaptation in Children with Acquired Brain Injuries
P04-20
Breu, M.; Höftberger, R.; Schuhfried, O.; Seidl, R.; Freilinger, M.: A Pediatric Case of Coincident Antibodies against the Acetylcholine Receptor and GM1 Ganglioside
P04-21
Lüsebrink, N.; Porto, L.; Kieslich, M.: Inherited Mitochondrial Neuropathy: Differential Diagnosis of Pediatric Axonal Neuropathy
P04-22
Opitz, D.; Blahak, C.; Wolf, C.; Lindmayer, F.; Kutschke, G.: Charcot-Marie-Tooth Phenotype with a 13-Year-Old Migrant: DD of Immune Neuropathy
P05-01
Husain, R. A.; Alhaddad, B.; Prokisch, H.; Mentzel, H. J.; Brandl, U.; Haack, T. B.: Leukodystrophy with Calcifications and Central Nervous System Atrophy: Expansion of the Phenotypic Spectrum Regarding Autosomal Recessive AARS Mutations?
P05-03
Aktas, O.; Gold, R.; Heyer, C.; Karenfort, M.; Kleiter, I.; Lukas, C.; Lücke, T.; Lutz, S.; Meier, U.; Mreyen, S.; Pöhlau, D.; Rostasy, K.; Schara, U.; Schipper, S.; Thiels, Ch.; von der Heiden, K.: Development of a MS-Network for Children and Adolescents in the Rhine-Ruhr Region
P05-04
Elpers, C.; Groß, C. C.; Althaus, J.; Fiedler, B.; Meuth, S. G.; Kurlemann, G.: Predictive Value of CSF Flow Cytometry in Pediatric Multiple Sclerosis
P05-05
Breuer, K.; Olze, A.; Borggräfe, I.; Gärtner, J.; Leiz, S.; Baethmann, M.: Leukoencephalopathy with Vanishing White Matter (VWM) Presenting with Early Myoclonic Encephalopathy (EME) and Rapid Progressive Internal Hydrocephalus
P05-06
Heinrich, B.; Steindl, K.; Gogoll, L.; Dünner, C.; Plecko, B.; Hackenberg, A.: In Delayed Myelination Count on T(o)3
P05-07
Matzker, E.; Gärtner, J.; Huppke, P.: Acute Severe Combined Demyelination: Case Report
P05-08
Hummel, H.-M.; Huppke, P.; Würfel, J.; Stark, W.; Ellenberger, D.; Friede, T.; Gärtner, J.: Sex-Related Differences in T2 Lesion Load in Pediatric Multiple Sclerosis Patients
P05-09
Rating, T.; Abeln, H.; Lasch, P.; Claßen, M.; Möller, K.; Kauffmann, B.: Posterior Reversible Encephalopathy Syndrome in a 6-Year-Old Female Patient with Steroid-Dependent Nephrotic Syndrome with Cyclosporine A Therapy
P05-10
Kölbel, H.; Kaiser, O.; Andres, B.; Taylor, A. F. M.; Kieslich, M.; Hoche, F.; Schara, U.: Gait Disturbances and Unspecific White Matter Hyperintensity in T2-Weighted Imaging as the First Manifestation of an Ataxia Telangiectasia
P06-04
Wegner, S.; Stephani, U.; Carlsson, G.; Hedderich, J.; Kopp, U. A.: Neuropsychological Aspects of Electroencephalographical Photosensitivity in Children and Adolescents
P06-06
Storch, K.; Smitka, M.; di Donato, N.; Hahn, G.; von der Hagen, M.; Schallner, J.: Rhombencephalosynapsis Leading to an Easily Missed, Underdiagnosed Neurocutaneous Syndrome
P06-08
Moein, G.; Porto, L.; Kieslich, M.: X-Linked Periventricular Heterotopia: Differential Diagnosis of Female Patients
P06-10
Sollmann, N.; Trepte-Freisleder, F.; Heinen, F.; Krieg, S. M.; Landgraf, M. N.: Repetitive Magnetic Stimulation of Neck Muscles in Patients with Migraine
P06-11
Becher, Th.; Hägele, A.; Weise, S.: Successful Therapy of Holmes Tremor with a Silicone Hand-Wrist Orthesis and Botulinum Toxin A
P07-01
Lühl, S.; Horvath, R.; Abicht, A.; Bode, H.; Kirschner, J.; Grünert, S. C.: Novel Homozygous Mitochondrial Arginyl-tRNA Synthetase 2 (RARS2) Gene Mutation without Pontocerebellar Hypoplasia Type 6
P07-02
Stange, M.; Prüfe, J.; Hartmann, H.; Meyer, U.; Das, A. M.: Neurocognitive Outcome in Hepatorenal Tyrosinemia
P07-03
Schuler, E.; Assmann, B.; Ziegler, A.; Opladen, T.; Hoffmann, G. F.: New Variant of Purine Nucleoside Phosphorylase Deficiency with Predominant Neurological Phenotype
P07-05
Kienle, N.; Marquard, K.; Blankenburg, M.; Spaich, C.; Fiedler, E.: Neurofibromatosis-Noonan Syndrome Due to a Newly Occurred Microdeletion 17q11.2
P07-07
Brösse, I.; Vogelsang, C.; Ziegler, A.; Hoffmann, G.: Everolimus as Targeted mTOR Inhibition in Neonates and Infants with Tuberous Sclerosis
P07-08
Gruber-Sedlmayr, U.; Hubmann, H.; Haidl, H.; Brunner-Krainz, M.; Schwerin-Nagel, A.; Schwerin-Nagel, A.; Kortschak, A.; Haber, E.; Sorantin, E.: Cerebral and Spinal Anomalies in One Monochorionic Twin with Schimmelpenning-Feuerstein-Mims Syndrome
P07-09
Schänzer, A.; Faas, D.; Shin, Y.; van Kuilenburg, A. BP.; Scarpa, M.; Kunze, A.; Zimmer, K. P.; Marquardt, T.; Hahn, A.: Markedly Elevated Chitotriosidase Activity and Enhanced Autophagy in Neonatal Andersen Disease (Glycogen Storage Disease Type IV)
P07-10
Cagnoli, S.; Herbold, T.; Prott, E.; Borusiak, P.: Variety of Phenotypes in Chromosome 16p11.2 Deletion Syndrome
P07-12
Bechtel, N.; Buiting, K.; Koch, M.; Speitel, K.; Noßwitz, U.; Horsthemke, B.; Wieczorek, D.; Rostásy, K.: Angelman Syndrome Caused by a Paternal Uniparental Disomy (UPD) 15 in a 2-Year-Old Boy of a Mother with a Robertsonian Translocation 14;15
P07-14
Decker, C.; Teig, N.; Abicht, A.; Holinski-Feder, E.; Köhler, C.; Dettmers, S.; Rossler, L.; Thiels, Ch.; Lücke, T.: Central Vocal Cord Paresis as Complication of a FBXL4-Associated Mitochondrial Depletions Syndrome
P07-15
Kutzbach, T.; Reich, L.; Wilken, B.; von der Hagen, M.; Mückschel, M.; Beste, C.: Assessing Cognition, Executive Functions, and Functional Brain Asymmetry in Children with Rett Syndrome
P07-17
Landgraf, M. N.; Heinen, F.: Neurological and Psychological Impairments of Children with Fetal Alcohol Spectrum Disorders: Two Case Reports
P07-18
Reutermann, J. E.; Traupe, O.; Hedderich, J.; Kaernbach, C.; Stephani, U.: Sympathetic Activity of PPR-Positive Adolescents: Clinical Study
P07-19
Maier, O.; Peterli, J.: Performing Evoked Potentials in Pediatrics: Methodology, Clinical Indications, and Limits
P07-20
Coci, E. G; Koehler, U.; Liehr, T.; Stelzner, A.; Fink, C.; Langen, H.; Riedel, J.: CANPMR Syndrome and Chromosome 1p32-p31 Deletion Syndrome Coexist in Two Related Individuals Affected by Simultaneous Haplo-insufficiency of CAMTA1 and NIFA Genes
P07-21
Nicolai, H.; Schröter, A.; Lücke, T.; Köhler, C.: Unclear Encephalopathy: Accurate Environmental History Conclusive!
P08-01
Becher, Th.; Weise, S.: Trichotillomania under a Therapy with Lisdexamfetamine
P08-03
Schuler, Elisabeth; Braun, Simon; Valente, André; Engert, Florian: Development and Evaluation of a Computer-Controlled System to Assess Associative Visual Learning and Memory in Zebrafish Larvae
P08-05
Weitkämper, A.; Teig, N.; Schauer, U.; Lücke, T.: Influence of Maternal Graduation on the Cognitive Development of Very Low-Birth-Weight Infants
P08-06
Spiegler, J.; Herting, E.; Göpel, W.: Very Low-Birth-Weight Infants in Germany: What about Early Intervention?
P08-07
Darekar, A. A.; Schreglmann, M.; Joy, H. M.; Gawne-Cain, M.; Kirkham, F. J.; Vollmer, B.: Susceptibility-Weighted Magnetic Resonance Imaging (SWI) in Newborns with Hypoxic-Ischemic Encephalopathy
P08-08
Reutlinger, C.; Isermann, J.; Niebuhr, U.: Use of an Electronic Version of the ICF-CY in a Rehabilitation Clinic
P08-09
Michel, J.; Jansen, C.; Wruk, M.; Dorsch, V.; Hessenauer, M.; Nastulla, T.; Kluger, G.; Berweck, S.: Botulinum Toxin in Paediatric Neuro-Rehabilitation
P08-11
Antenbrink, F.; Sandrieser, T.; Hoppen, T.; Lorey, M.; Nüßlein, T.: Severe Birth-Related Spinal Trauma – A Case Report with Video Presentation
P08-12
Hüning, B.; Assing, B.; Weishaupt, E.; Felderhoff-Müser, U.; Zmyj, N.: Delay of Gratification in Preterm Infants Born under 32 Weeks of Gestation at the Age of 4 Years and Correlation with Time Comprehension
P08-13
Schreglmann, M.; Helps, S.; Hart, D.; Vollmer, B.: How Useful Is General Movement Assessment and Alberta Infant Motor Scale at the Age of Three Months for Prediction of Neuromotor Outcome in an Unselected Group of High-Risk Infants?
P08-14
Jung, S.; Ballheimer, Y.; Brackmann, F.; Trollmann, R.: Age-Specific Changes of the AMPA Receptor and ADAR Enzyme Expression Profile in the Neonatal Mouse Brain due to Pilocarpine-Induced Seizures