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

Abstracts (HTML) List of Authors

Lackner, H

Infantile Alexander Disease mimicking multilocular astrocytoma

Latal, B

Cerebral MRI findings in adolescents with congenital heart disease

Laufs, M

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
De novo deletion 17p13.1 and duplication 17p11.2 in a seven months-old male infant with the clinical features of Potocki-Lupski syndrome
DWI and Proton weighted MRI seems to be a highly sensitive marker of pathological activity in pediatric multiple sclerosis

Lebrun, AH

Identification of potential biomarkers and modifiers of CLN3-disease progression

Lee-Kirsch, AE

ADAMTS13 dysfunction and a novel frameshift mutation in the TREX1 gene in a patient with Aicardi-Goutières syndrome

Leis, T

Preterm and small-for-gestational age: no risk for an adverse cognitive development?

Leiz, S

Intracranial hypertension in a boy with infantile hypophosphatasia requiring shunt installation

Lengnick, K

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

Letzgus, A

Psychiatric symptoms and CK-Elevation as initial manifestations of late-onset Tay-Sachs disease

LeVan, P

HFOs (80–450Hz) recorded with standard intracranial electrodes reflect epileptogenicity in children with focal cortical dysplasia
Dynamic analysis of absence seizures in humans: all the same but all different

Lewis, T

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

Lidzba, K

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

Lindbichler, F

Presentation of 16 paediatric patients manifesting with stroke during 2006–2010

Linder-Lucht, M

Application of Array-based Comparative Genome Hybridization in patients with mental retardation

Lorenz, I

Reflex epilepsy in demyelinating encephalopathy – a case report

Lücke, T

L-2-hydroxyglutaric aciduria: Infantile versus adult late-onset manifestation
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)
MRI abnormalities associated with Vigabatrin treatment – a longitudinal case study and an atypical case
Use of guidelines improves the neurological outcome in glutaric aciduria type I
Neurological complications following renal transplantation in infants and children: A retrospective single centre study

Lütjen, S

Remi-Pro: a standardized method to document the course of remission and finding of therapeutic goals in children and adolescents after severe acquired brain-lesions

Lütschg, J

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