Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Gädeke, JC

Intra- and cross-modal refractory period effects in healthy children and adults: An ERP study

Gallistl, S

Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports

Ganslandt, O

Closure of meningomyeloceles with the 4-flap compound technique according to Ramirez
Ultrasound-guided neuronavigation-the safest approach for Rickham capsule insertion in preterm infants

Garavaglia, B

Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation

Garkisch, S

Mutation analysis of KCNAB1 in rolandic epilepsy

Gärtner, J

Autosomal-recessive Kearns-Sayre syndrome is caused by mutations in the RRM2B gene with altered mitochondrial transcription
Alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism: Phenotypic spectrum of ATP1A3-associated disorders
Alternating hemiplegia of childhood is caused by heterozygous de novo mutations in the ATP1A3 gene: The expanding mutational spectrum of ATP1A3-related dystonic movement disorders
Evidence against the concept of chronic cerebrospinal venous insufficiency in multiple sclerosis
Disequilibrium syndrome caused by an unusual constellation of VLDLR mutations
Stepwise adaptation of treatment with calcium folinate in different modes of application leads to optimal therapeutic results for patients with cerebral folate transport deficiency
Apheresis in the treatment of an acute attack of a demyelinating central nervous system disorder
Mitochondrial encephalomyopathy presenting with deafness, mutism, ataxia and late onset external ophthalmoplegia caused by a mutation in the X-linked gene AIFM1

Gaser, C

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Gassner, S

Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions

Gattinger, N

A physiological characterization of biphasic transcranial magnetic stimulation
Induction of cortical plasticity by biphasic quadro-pulse stimulation

Gautsch, K

Epileptic seizures and chromosomal microdeletions/duplications

Gburek-Augustat, J

Specific pontine MRI-pattern is a helpful marker to recognize ataxia Charlevoix-Saguenay

Gedik, A

Visual disorders in children with cerebral palsy
Epilepsy in children with cerebral palsy

Geis, T

Genotype-phenotype correlation in congenital muscular dystrophies with defective O-glycosylation of #CHR:alpha_LOWER#-dystroglycan

Giagkou, E

Neurodegeneration with brain iron accumulation type 4 by mutation in the C19orf12 gene: first time found in adolescent of Russian origin

Giner, T

Status epilepticus caused by hypocalcaemia in a 6-month old child with hypoparathyroidism

Gleich, B

A physiological characterization of biphasic transcranial magnetic stimulation
Induction of cortical plasticity by biphasic quadro-pulse stimulation

Goebel, HH

Molecular mechanisms of juvenile dermatomyositis

Goelz, R

Increasing prematurity is associated with a more pronounced delay in brain maturation in older children and adolescents

Gold, R

A prospective study on 71 children to investigate normative pediatric values in optical coherence tomography
Visual impairment – differential diagnoses

Göpel, W

Do developmental problems perceived by parents of very-low-birth weight infants during the first year of life correlate with objective criteria at 2 years of age?

Gosk, M

Progressive myoclonus epilepsy: a differential diagnosis from juvenile chorea Huntington disease

Gospe, S

Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial

Gramsch, K

Current care practice in Duchenne muscular dystrophy in Europe – results of the CARE-NMD cross-sectional survey

Granel, M

Intraventricular baclofen therapy in refractory secondary dystonia-Indication, methodology, safety, and first results
Severe dystonia caused by hemolytic-uremic syndrome with characteristic MRI scans

Grasl, C

Guidelines and examples for orthotic treatment of children and youth in case of myelomeningocele

Gröschel, S

Loss of speech in late-infantile and juvenile metachromatic leukodystrophy

Grosse, R

Longitudinal Evaluation of Brain Iron Depositions in a Patient With Confirmed c19orf12 Mutation Using R2* Relaxometry and Quantitative Susceptibility Mapping

Gruber-Sedlmayr, U

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports
PANK2 disease with early onset: clinical and radiologic findings under short term treatment with deferiprone
Anti-NMDAR encephalitis in children: Delineation of the epileptic phenotypes and EEG findings
Rigorous investigation of opsoclonus-myoclonus-syndrome associated neuroblastoma: three case reports
Antibodies against Mycoplasma pneumoniae in three patients with meningoencephalitis-causal relationship or epiphenomenon?
Tuberous sclerosis complex-successful therapy with everolimus
Autologous stem cell transplantation – a therapeutic option in childhood onset chronic inflammatory demyelinating polyneuroradiculopathy?

Grulich-Henn, J

Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Grummel, V

Inward rectifying potassium channel KIR4.1-specific antibodies in children with acquired demyelinating CNS disease

Guerrini, R

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
Effectiveness of antiepileptic therapy in catastrophic infantile epilepsy: Comparison of patients with SCN1A and PCDH19 mutations

Gumpold, C

Analysis of myogenic and endothelial progenitor cells in muscle biopsies of juvenile dermatomyositis

Güngör, T

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation