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

Abstracts (HTML) List of Authors

Pagel, B

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

Paglioli, E

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Palmini, A

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Panzer, A

Could a mutation in the TGIF-1 gene result in phenotypical expressions like pachygyria, intracerebral calcification, and neonatal epilepsy?

Pape, L

Neurological outcome in pediatric patients with hemolytic uremic syndrome caused by Escherichia coli O104:H4

Parkin, N

Congenital myopathy or neurofibromatosis type 1?

Paschke, E

Pyridoxine-dependent epilepsy: case report
PNPO mutations in patients with pyridoxine dependent epilepsy

Pascoal, T

Immediate improvement of paretic hand function after epilepsy surgery in congenital hemiparesis

Paul, K

PNPO mutations in patients with pyridoxine dependent epilepsy

Pauls, A

Young adults with dyskinetic cerebral palsy improve subjectively on pallidal stimulation but not in formal dystonia, gait, speech, and swallowing testing

Paulus, W

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Pein, H von

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Pellacani, S

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

Peterli, J

Evoked potentials in pediatrics: options and limits

Peters, J

Fatal outcome in a case of recurrent acute necrotizing encephalopathy with RANBP2 gene mutation: importance and difficulty of an early MRI pattern recognition

Philip, S

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

Pieper, T

Coincidence of duplication in the PCDH 19 gene and focal cortical dysplasia
Hemimegalencephaly: involvement of cranial nerves and intracranial vessels
Stereo-EEG in children with therapy-refractory epilepsies: Robot-assistance plus stereotaxy combines speed with maximal precision for the implantation of multiple depth electrodes

Piepkorn, M

Herpes simplex virus encephalitis – an unexpected relapse with choreoathetosis

Pietz, J

Implementation of a (neuro-)psychological screening of infants with newly diagnosed epilepsy. Practicability and first results concerning potential premorbid problems
Atypical Infantile neuroaxonal dystrophy: a case report
Behçet disease – a rare differential diagnosis of inflammatory CNS disease in children

Pietzsch, S

Dramatic neurological signs in children with intussusception

Plecko, B

Differential diagnosis of central nervous system vasculopathies: two 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
Infantile choreatic movements, early onset severe epileptic encephalopathy, and primary developmental impairment as a result of a de novo missense mutation in the SCN2A gene
Management algorithm in newly diagnosed European moyamoya angiopathy: One year experience at the Moyamoya Center, University Children's Hospital Zurich
Pyridoxine-dependent epilepsy: case report
Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype
Lysine restricted diet for pyridoxine-dependent epilepsy: First reports and future trial
Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation
PNPO mutations in patients with pyridoxine dependent epilepsy

Pless, M

Unusual prodromal manifestation of neuromyelitis optica with prolonged seizures, fever, CSF pleocytosis and encephalopathic EEG-pattern

Poggenburg, I

Anti-N-methyl-d-aspartate-receptor-encephalitis

Pohlig, K

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

Polster, T

Microcephaly-capillary malformation syndrome: Delineation of a new syndrome

Pons-Kühnemann, J

Mutation analysis of KCNAB1 in rolandic epilepsy

Poretti, A

Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum
Hemimegalencephaly: involvement of cranial nerves and intracranial vessels
Maturation of the brainstem and cerebellar white matter tracts from the neonatal period to adolescence: a diffusion tensor imaging study
Ataxia, cognitive impairment, and ocular motor apraxia with cerebellar cysts and dysplasia: A new form of dystroglycanopathy?

Porto, L

Atypical case of a neurocutaneous melanosis with typical magnetic resonance imaging findings
Absent biochemical evidence at an early age delayed diagnosis in a patient with a clinically severe form of peroxisomal biogenesis disorder

Poschmann, S

Pseudomigraine with temporary neurological symptoms and lymphocytic pleocytosis in a 14-year-old girl probably associated with celiac disease

Prager-Puntigam, S

Vagal nerve stimulator in childhood absence epilepsy: 2 case reports
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?

Preisinger, A

Facial nerve palsy in children – is it as benign as supposed?

Preusse, C

Molecular mechanisms of juvenile dermatomyositis

Prietsch, V

Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions

Pritsch, M

Acute hemiataxia in childhood

Prokisch, H

Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
Treat Iron-Related Childhood-Onset Neurodegeneration (TIRCON) – an integrated strategy under FP7 to improve research, treatment, and care in neurodegeneration with brain iron accumulation
Clinical symptoms of six children with thiamin pyrophosphokinase deficiency
Exome sequencing in 30 neurodegeneration with brain iron accumulation patients
Mitochondriopathy due to mutations in MTFMT: a predominant neurologic phenotype
Molecular diagnosis in mitochondrial respiratory chain deficiency using exome sequencing
The German network for mitochondrial disorders (mitoNET)

Prölß, AK

Quantification of muscular morphological alterations in patients with infantile and early-juvenile Pompe disease

Prott, EC

Nicolaides-Baraitser Syndrome

Prüfer, M

Rituximab and Cyclophosphamide as an alternative in immunomodulatory therapy in Rasmussen encephalitis

Pupp-Peglow, U

Predictors of academic difficulties in preterm children compared with term-born children at the age of 5 years

Püst, B

Retrospective evaluation of antiepileptic drugs in patients with CDKL5 mutations
Paroxysmal dyskinesia due to PRRT2 mutation in 15-year-old female patient with benign familial infantile convulsions
Isolated trochlear palsy in Lyme disease may persist
13-year-old girl with antiphospholipid antibody-related chorea