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

Abstracts (HTML) Autorenliste

Wagner, A

Long-term outcome of Alice-in-Wonderland-Syndrome: Results from a case series of 12 patients

Walkenhorst, H

Lupus erythematosus and Aicardi-Goutières Syndrome: a continuum of immune mediated diseases

Walsh, S

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

Walter, M

Laboratory diagnostics of Canavan Disease using EBV-transformed lymphocytes

Weber, K

Asymmetrical localisation of the motor cortex after perinatally acquired intracerebral hemorrhage: Volume shift versus neuroplasticity

Wehrli, E

Differences in risk-factors, aetiology and outcome between children and young adults with acute ischaemic stroke

Weigt-Usinger, K

BARTH SYNDROME with a new mutation without cardial involvement
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)

Weise, S

MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case

Weiss, D

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

Weissert, M

Leigh Syndrome: typical phenotype but atypical mitochondrial mutation – a case report

Weitkämper, A

BARTH SYNDROME with a new mutation without cardial involvement

Wenzel, D

Reflex epilepsy in demyelinating encephalopathy – a case report
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?

Weschke, B

Clinical neurophysiology for differentiation between Pelizaeus-Merzbacher Disease and Pelizaeus-Merzbacher-like Disease

Wessel, V

Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity

Westhoff, B

„Fixed dystonia“ syndrome after peripheral trauma in two adolescent girls

Wevers, RA

Towards the genetic defect in MEGDEL syndrome: Four novel patients

Wiegand, C

Experiences with Laparoscopic Adjustable Gastric banding (LAGB) and Sleeve Gastrectomy (SG) in the treatment of patients with childhood craniopharyngioma and morbid obesity

Wiegand, G

Functional hemispherotomy for refractory epilepsy in pediatric patients: the right person at the right time

Wiesel, T

The use of Quantitative sensory testing for sensible diabetic neuropathy in children and adults

Wilichowski, E

Autosomal dominant congenital myopathy with fibre type disproportion due to mutation in the α slow-tropomyosin gene

Wilke, M

Somatosensory system in congenital hemiparesis: clinical assessment and resting state functional connectivity MRI analysis
Metachromatic Leukodystrophy: spatial and temporal pattern of MRI changes and their association with motor deterioration
Feasibility of functional MRI in children and adolescents with neurological disorders – the Vogtareuth experience

Willichowski, E

Phenotype and long-term follow-up of juvenile Selenoprotein N1-related myopathy (SEPN1-RM)

Wimmer, K

Neurofibromatosis type 1 and Arnold-Chiari-malformation. An unknown association?

Winkler, S

Language abilities after early left-hemispheric lesions – neural and cognitive compensation
Language abilities after early left-hemispheric lesions – Production and comprehension of complex linguistic structures

Wittke, A

Visual attention performance in term born and preterm infants with different perinatal risk

Wochner, K

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

Woermann, G

MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case

Wolf, A

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

Wolff, M

Eyelid myoclonia with absences (Jeavons syndrome): An unrecognized generalized epileptic syndrome?
Intensive immunmodulatory therapy in a 3 year old child with anti-NMDA-receptor encephalitis

Wolff, S

EEG-fMRI: Including sleep-induced potentials in the general linear model improves spatial accordance with epileptic focus

Wortmann, SB

Towards the genetic defect in MEGDEL syndrome: Four novel patients

Wraige, E

Dopamine transporter defect: Infantile parkinsonism-dystonia with elevated dopamine metabolites in cerebrospinal fluid is genetically resolved

Wyatt, J

Microstructural alterations of motor pathways in adolescents born preterm