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

Abstracts (HTML) List of Authors

Ranke, M

Relationship between growth and psychomotor development of preterm children

Reiser, M

Secondary cerebrovenous outflow in relation to duration of disease in patients with multiple sclerosis

Renneberg, A

Multifocal Balo's concentric sclerosis in a 10-year-old German boy

Rettinger, N

Short vertigo attacks in childhood: vestibular paroxysmia

Reuss, R

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

Reutlinger, C

Clinical characterization of myoclonic-astatic epilepsy

Richter, M

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

Rieger-Fackeldey, E

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Riess, A

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

Rieß, J

3D-Television and the Risk of Seizures in Children

Rittinger, O

Intranasal insulin may influence motor activities and behaviour in Phelan McDermid Syndrom

Rocamora Zuñiga, R

Mutations in PCDH19 and Epilepsy: Presentation of a Spanish family with phenotypic heterogeneity

Rodemann, S

Relationship between growth and psychomotor development of preterm children

Rohrbach, M

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

Rohrschneider, K

Encephalocraniocutaneous lipomatosis (ECCL) – a case report

Rompel, O

Risk factors for progression to Multiple Sclerosis after Optic Neuritis

Rosenbaum, T

Sleepless flies – Clinical and molecular genetic characterization of sleep disturbances in neurofibromatosis

Rosner, V

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

Rost, I

A new de novo deletion 4q13.2q13.3 in a patient with mental retardation, growth retardation and various facial and skeletal dysmorphic features

Rostásy, K

Pediatric herpes simplex virus encephalitis: a critical multicentric analysis
Long-term outcome and MRI findings in children with acute cerebellitis
A novel variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy and hearing loss – a differential diagnosis in floppy infant syndrome

Rübel, A

An opel-label, multi-center, expanded access study of RAD001 (Everolimus) in patients with TSC SEGA

Rückauer, K

Mowat-Wilson Syndrome, a rare genetic condition with intestinal and cerebral symptoms

Rückriegel, S

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

Rudnik-Schöneborn, S

FIRES (febrile infection-related epilepsy syndrome) partially responsive to magnesium and dextromethorphan treatment

Rupprich, K

A 16 year-old patient presenting with Lambert-Eaton myasthenic syndrome