Abstracts of the 36th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Danz, B

Current practice in the management of newborns with spina bifida in Germany

Das, A

L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation

Das, AM

Neurological complications following renal transplantation in infants and children: A retrospective single centre study

de Brouwer, APM

Towards the genetic defect in MEGDEL syndrome: Four novel patients

Deiters, L

Neurodevelopmental long-term outcome in VLBW preterm infants born in 2000–2004
Preterm and small-for-gestational age: no risk for an adverse cognitive development?

Dekomien, G

Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease
Muscular hypotonia, joint contractures and elevated creatin kinase level as main symptoms for Congenital muscular dystrophy 1A (MDC 1A/congenital muscular dystrophy with laminin α 2 (merosin) deficiency)

Della Marina, A

ARX-mutation – phenotype and clinical course in two brothers with West Syndrome and developmental delay

Delvendahl, I

Low-Frequency rTMS selectively modulates inhibitory intracortical networks
Impaired motor cortex plasticity in patients with Noonan syndrome
Influence of current direction in transcranial magnetic stimulation (TMS) on MEP amplitude and latency – opportunity of I wave specific evaluation and stimulation

Demir, Z

Temporary neonatal respiratory disorder – Early-onset-variation of Ondine's curse

Denecke, J

Pontine tegmental cap dysplasia: case report of a „new“ disorder with associated cortical malformation

Deppe, M

Diffusion tensor imaging demonstrates effectiveness of immunotherapy for Rasmussen's encephalitis

Deppe, W

Constraint-induced movement therapy (CIMT) for hemiparetic children in comparison to bimanual treatment – what is (more) effective?

Dercks, M

Specific motion patterns of the sagittal, frontal and transversal plane in children with bilateral spastic cerebral palsy: Preliminary results of a cross-sectional study
Robotic-assisted gait training improves gait parameters and functional mobility in patients wit cerebral palsy – preliminary results of a longitudinal study

der Hagen, M von

Case report of a 1-year old girl with β-ureidopropionase deficiency and development of cystic encephalomalacia
Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)

De Sonneville, L

Impairment of executive functions in pediatric posterior fossa tumor survivors

Dickhaus, H

Evaluation of general movements in infants with an electromagnetic tracking system – first steps towards the discrimination of variability of spontaneous movements

Diekmann, S

RNASET2-deficient cystic leukoencephalopathy: a new lysosomal disorder

Ding, XQ

L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation

Dinomais, M

Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis

Dittrich, S

Calpainopathy as differential diagnosis of idiopathic hyperCKemia
Autosomal dominant CMT-Type IB (Charcot-Marie-Tooth Neuropathy) as a differential diagnosis of clinically diagnosed autosomal recessive demyelinating CMT-Type 4E
Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis

Döbler-Neumann, M

Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?

Dossal, S

Long-term follow up of preterms below 33 weeks of gestation at school age

Drabsch, C

From pediatric to adult-orientated care: the „Berliner Transitionsprogramm“

Dreha-Kulaczewski, S

Clinical signs and treatment of cerebral folate transport deficiency, a novel inherited disorder of folate metabolism

Dresel, R

Dysembryoplastic neuroepithelial tumor (DNET) in a patient with Noonan syndrome

Driess, J

Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes

Dubeau, F

Dynamic analysis of absence seizures in humans: all the same but all different

Dümpelmann, M

HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia