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Springerplus|November 7, 2015
Opsoclonus-myoclonus syndrome after adenovirus infectionSteffen Syrbe, Andreas Merkenschlager, Matthias K Bernhard, et al.
Brain & Development|June 12, 2013
Wide spectrum of clinical manifestations in children with tuberous sclerosis complex--follow-up of 20 childrenRoland R Mettin, Andreas Merkenschlager, Matthias K Bernhard, et al.
Klinische Padiatrie|September 11, 2019
[The Cognitive, Language and Motor Development of Prenatal Methamphetamine- and Opioid-exposed Children]Juliane Schreiter, Mandy Vogel, Henriette Kiep, et al.
Journal of Neurosurgery. Pediatrics|September 5, 2015
Adult long-term health-related quality of life of congenital hydrocephalus patientsAnja Kutscher, Ulf Nestler, Matthias K Bernhard, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 8, 2015
Signs and symptoms of pediatric brain tumors and diagnostic value of preoperative EEGMatthias Preuß, Sophia Preiss, Steffen Syrbe, et al.
Epilepsy & Behavior : E&B|April 27, 2016
Epilepsy in children and adolescents: Disease concepts, practical knowledge, and copingJosefine Pauschek, Matthias K Bernhard, Steffen Syrbe, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|November 29, 2015
Use of complementary and alternative medicine (CAM) by parents in their children and adolescents with epilepsy - Prevelance, predictors and parents' assessmentNicole Hartmann, Martina P Neininger, Matthias K Bernhard, et al.
Archives of Disease in Childhood|June 27, 2015
Knowledge and attitudes of school teachers, preschool teachers and students in teacher training about epilepsy and emergency management of seizuresHenriette K Dumeier, Martina P Neininger, Matthias K Bernhard, et al.
European Journal of Pediatrics|August 13, 2013
Initial anticonvulsant monotherapy in routine care of children and adolescents: levetiracetam fails more frequently than valproate and oxcarbazepine due to a lack of effectivenessAstrid Bertsche, Martina P Neininger, Anna J Dahse, et al.
Molecular Syndromology|October 27, 2016
Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal SeizuresSnezana Maljevic, Sabina Vejzovic, Matthias K Bernhard, et al.
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