Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Bächli, H

Minimal invasive fetoscopic closure of myelomeningocele – postoperative care and interdisciplinary disease-management

Baethmann, M

Gastroenteritis associated encephalopathy with reversible splenial lesion: three cases

Banwell, B

Hiccups, Vomiting and the Brain

Barkmann, C

Statistical properties of the jNCL scoring system according to Kohlschütter (1988)

Bartels, I

Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma
Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Barthelmie, A

Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)
Deletion 22q13 (Phelan-McDermid-Syndrom) in two children with delayed development of speech and muscular hypotonia

Bast, T

Clinical characterization of myoclonic-astatic epilepsy

Baumann, M

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Bäumel, C

3D-Television and the Risk of Seizures in Children

Baumgart, A

The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Baumgartner, M

Male Rett Syndrome – genetic diagnosis using oral mucosa swabs

Baumgartner, S

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis

Baz-Bartels, M

Ataxia Telangiectasia (AT) as a radiation sensitivity syndrom and limits of radiotherapeutic intervention

Becher, T

Neuroborreliosis without Neurology?!
Focal epilepsy caused by multiple cavernous hemangiomas and mental retardation – successful therapy and genetic cause (CCM3)

Beck, M

Respiration and its correlation with motoric function in non-classic Pompe disease
Treatment of Lysosomal Storage Disorders: Presence and Future

Berghoff, M

mRNA-expression patterns of Fas and its signalling cascade in Multiple Sclerosis (MS) and Experimental Autoimmune Encephalomyelitis (EAE)

Bernhard, M

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?
Shaking the head without end – bobble-head doll syndrome in no-no direction

Bertsche, A

Cerebellar Infarction and Coarctation of the Aorta – causal relation or coincidence?
Shaking the head without end – bobble-head doll syndrome in no-no direction

Berweck, S

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis
Long-term Outcome after Vegetative State due to Near-Drowning and Quality of Life of the Families
Ipsilateral Motor Control Without Mirror Movements?

Bettendorf, U

Influence of antiepileptic treatment on bone metabolism

Bevot, A

Relationship between growth and psychomotor development of preterm children

Beytia, M

Manifestation of muscular dystrophy by Anoctamin-5 mutation in infancy

Biebl, A

Prospective analysis on brain MRI in children with neurological disease

Bierbaum, A

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Biesecker, L

A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Bigi, S

Hiccups, Vomiting and the Brain

Binggeli, R

Neuroleptic Malignant Syndrome due to Tetrabenazine in a Boy with a Subacute Extrapyramidal Disorder

Biskup, S

A familial epilepsy with behavioural features associated with a PCDH19 mutation

Bittner, R

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Blankenburg, M

Peroneal nerve palsy pointing towards a cerebral disorder
Impaired Control of Respiration as Crucial Evidence for Pitt-Hopkins Syndrome

Blaschek, A

Familial mutation in ACTA1 gene – clinical variability
Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis
Multiple sclerosis and periodic fever syndromes: Characterization of clinical symptoms

Blassnig-Ezeh, A

Central nervous system Lyme disease – Presentation of two cases

Bode, H

Predictors of comorbid psychiatric disorders in children and adolescents with cerebral palsy. Impact on family burden and quality of life. Results of a multicenter study

Böhm, R

Symptomatic Treatment of Tomaculous Polyneuropathy with Methylprednisolone

Böhringer, E

Isolated neonatal bilateral palsy of the n. radialis; case report and review of the literature
Mosaic ring chromosome 3 in a child with epilepsy and developmental delay

Boltshauser, E

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia
Oral-Facial-Digital Syndrome Type VI: Delineation and Diagnostic Criteria
Macrocerebellum: not a clinical and neuroimaging entity
Behavioural changes and unilateral movement disorder in 2 adolescents with Chorea Sydenham
Bannayan-Riley-Ruvalcaba-Syndrom with progressive spinal epidural lipomatosis

Bonin, M

Large interstitial duplication in the LARGE-gene in a patient with Walker-Warburg-syndrome.

Bönnemann, C

A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Boor, R

Clinical characterization of myoclonic-astatic epilepsy
The role of vitamin B6 deficiency in infantile epilepsies of unknown etiology

Borggräfe, I

Immunoadsorption in refractory status epilepticus related to NMDAR-Encephalitis
Presurgical evaluation in refractory epilepsy in toddlers with depths electrodes

Borusiak, P

Influence of antiepileptic treatment on bone metabolism

Bozinov, O

Isolated spinal juvenile xanthogranuloma in an infant presenting as acute paraplegia

Brackmann, F

Age dependent regulation of the neuroprotective factor activin in the mouse brain

Brentrup, A

Rare course of an intraspinal dermoid

Brockmann, K

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?
A familial epilepsy with behavioural features associated with a PCDH19 mutation
A postzygotic activating AKT1 mutation in a discordant monozygotic twin with Proteus syndrome

Broser, P

Lateralization of language pathways in children as assessed using fMRI-guided probabilistic tractography

Brueckner, F

Pseudotumor cerebri in an 8 month old infant

Brüggemann, N

Do young adolescents with periodic ataxia due to GLUT-1 Deficiency profit from introduction of a modified Atkins Diet?

Brunner-Krainz, M

CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura
Chronic inflammatory bowel disease and cerebrovascular insults in a pediatric patient: a case report
Bannayan-Riley-Ruvalcaba-Syndrome – a rare differential diagnosis in children with macrocephaly

Budde, J

Pseudotumor cerebri under prednisolone treatment for infantile spasms

Bültmann, E

Fluctuating N IV paresis as presenting sign of a brain stem tumor: two pediatric cases

Burfeind, P

Array CGH in children and adolescents with developmental delay or intellectual disability: are there phenotypic clues to clinically relevant chromosomal microaberrations?

Burger, H

Integration of Armeo Spring Pediatrics in inpatient Rehabilitation of children and adolescents with Hemiparesis

Burghardt, R

Laterality, bimanual interference and short-term motor learning of fine motor movements in childhood and adolescence

Bürki, S

Video documentation of a case of Dopa responsive Dystonia in early infancy: a rare but important diagnosis

Bußmann, C

Leukoencephalopathy with metaphyseal chondrodysplasia

Buyse, G

DELOS Phase III Study with Idebenone (Catena®) in Duchenne Muscular Dystrophy