Abstracts of the 35th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Bajer-Kornek, B.

Epidemiology of pediatric multiple sclerosis in Austria

Baldeweg, T.

Language lateralisation in childhood-onset focal epilepsy: Evidence from fMRI

Balmer, C.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Bast, T.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient

Baudhuin, J. A.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®

Baumann, M.

Uncommon manifestations of childhood neuroborreliosis

Baumgartner, M.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development

Baumhackl, U.

Epidemiology of pediatric multiple sclerosis in Austria

Becher, T.

Sandifers syndrome – Unusual case report and review of the literature
Dystonic movements and developmental coordination disorder – Successful treatment with methylphenidate

Beck, M.

GM1 gangliosidosis and Morquio B disease: Expression analysis of missense mutations affecting the catalytic site of acid β-galactosidase

Becker, M.

Modified memory processes in children with febrile seizures: Analysis of event-related potentials

Beckhaus, M.

A series of 34 patients with Rasmussen's encephalitis: Clinical course, EEG- and MRI findings

Benninger, F.

Long-term use of the ketogenic diet in drug resistant epilepsy syndromes during childhood: Differences between responders and non-responders in seizure types, EEG, and outcome

Ben-Omran, T.

GLUT1 deficiency syndrome in a consanguineous Arab family carrying a novel homozygous missense mutation

Bernhard, M. K.

Seizures caused by accidental dimenhydriante intoxication
Toxic effects of lamotrigine ingestion in children
Miller Fisher syndrome and Guillain Barré syndrome with ophtamloplegia: Two cases with overlapping phenotype
Therapy of headaches in children and adolescents with TENS (Transcutaneous Electrical Nerve Stimulation) – An observational study of the Children's Hospital of the University of Leipzig
Chronic fatigue and pain syndrome caused by persistent intoxication with cactus spurge in a 12-year-old girl

Bertsche, A.

Hashimoto's encephalopathy with stroke-like episodes and optic neuritis in a 19-year-old patient
GLUT1 deficiency in a child with a movement disorder

Berweck, S.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Hip development in children with cerebral palsy and adductor spasticity treated with botulinum toxin type A: A two-year follow-up
Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia
Diffusion tensor imaging (DTI) of callosal motor fibers correlates with functional impairment in children with periventricular leukomalacia

Bevot, A.

Polyneuropathy and hepatopathy as an infantile manifestation of a POLG1 gene defect

Bien, C. G.

Anti-N-methyl-D-aspartate (NMDA) receptor encephalitis in a 12-year-old girl: Typical symptoms help to consider diagnosis of this new treatable disorder

Bigi, S.

Bannwarth's syndrome – A rare but important manifestation of neuroborreliosis in childhood
Therapy of sinus venous thrombosis in childhood – A standardised treatment protocol – Call for participation

Birnbacher, R.

Uncommon manifestations of childhood neuroborreliosis

Biste, M.

Improved molecular diagnostics for patients with respiratory chain complex deficiency

Bittner, R.

Severe central hypomyelination in an infant with mtDNA depletion caused by RRM2B gene mutations

Blankenburg, M.

Quantitative Sensory Testing (QST) in children and adolescents

Blaschek, A.

Clinical long term follow-up of children presenting with a severe acute disseminated encephalomyelitis (ADEM)

Boekens, H.

Quantitative Sensory Testing (QST) in children and adolescents

Böhmer, S.

Copper histidine therapy started in a boy at the age of three years – Treatment option for a mild form of Menkes's disease

Boltshauser, E.

Infantile Pompe's disease under enzyme replacement therapy: Marked cognitive and speech delay but practically normal motor development
Life with only one half of the cerebellum: Outcome in children with severe unilateral cerebellar hypoplasia
Pontine tegmental cap dysplasia: Two additional cases

Boor, R.

Rufinamide treatment in 18 patients with Lennox-Gastaut syndrome – Documentation with the electronic patient diary epivista®
Screening for 15q13.3 microdeletions in Benign Rolandic Epilepsy and related syndromes

Boppel, T.

Deep brain stimulation in children and adolescents with dystonia

Borggraefe, I.

Safety of botulinum toxin treatment in children with cerebral palsy in correlation to GMFCS level
Correlation of botulinum toxin dosage and GMFCS level in children with bilateral spastic cerebral palsy – An explorative cohortstudy
Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Borggräfe, I.

Interventional-neuropaediatric spectrum of treatments with botulinum neurotoxin type A, free of complexing proteins: Effective and safe application – Three exemplary cases
Robotic-assisted treadmill therapy enhances motor functions in children with bilateral spastic cerebral palsy

Bötzel, K.

Severity and DYT1 status predict outcome after chronic bilateral pallidal stimulation in children and adolescents with primary generalized dystonia

Braulke, T.

Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian sibship

Breuer, K.

Monosomy 9pter-p22 in a boy with neonatal hypoglycemia, epilepsy, facial dysmorphism and hypotonia

Brocke, K. S.

Microdeletion 4p16.3 that includes Wolf-Hirschhorn syndrome critical region – A case report

Brockmann, K.

Ophthalmoplegic migraine (OM) with early-onset recurrent oculomotor palsy of the left eye in a 6-year-old boy

Brück, W.

Natalizumab in 4 cases of pediatric multiple sclerosis

Brunner-Krainz, M.

20 years evaluation of pediatric patients with encephalitis in the PICU
Febrile seizures – First symptom of Rasmussenencephalitis
Homocystein as an important diagnostic marker of remethylation defects – A case report

Burdach, S.

Hennekam-syndrome with unusual MRI-changes and symptomatic epilepsy

Burfeind, P.

CDKL5 mutation in neonatal onset of epilepsy