Abstracts of the 31st Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)

Abstracts (HTML) List of Authors

Paetau, R.

Comparison of interictal EEG and MEG I: MEG detects a higher ratio of focal interictal epileptic discharges in sleep

Pagenstecher, A.

Inhibition of ependymal flow during brain development: A novel mechanism for hydrocephalus formation

Pahs, G.

Behavior problems in patients with juvenile myoclonic epilepsy (JME)

Pantazis, G.

Parry-Romberg-Syndrom and Rasmussen-encephalitis: A case report

Panteliadis, C.

Effectiveness of intermittent diazepam in febrile convulsions: A long term prospective controlled study
Short-term, low-dose ACTH therapy in West syndrome

Parbel, S.

Low CSF branched chain amino acids: Evidence for increased brain glutamate synthesis due to impaired mitochondrial function?
Muscle eye brain disease – phenotype of glycosylation deficiency?
Subacute metabolic stroke in two patients with propionic acidemia with fatal and good outcome
Increased CSF ratio of glutamine to branched chain amino acids in DOPA non responsive but gabapentin responsive dystonia

Pascher, B.

A severe case of Aicardi syndrome with triple X
Subcutaneous microdialysis – a safe and minimal-invasive method for biochemical tissue monitoring in mitochondrial diseases
Biochemical therapy monitoring with subcutaneous microdialysis in mitochondrial encephalomyopathies
Changes in carnitine metabolism in children with intractable epilepsy under ketogenic diet, demonstrated by subcutaneous microdialysis
Efficacy of the ketogenic diet in children with pharmacoresistant epilepsies

Paschke, E.

Cooper concentration of liver tissue under cooper histidin therapy in a patient with Menkes disease

Pascual, J. M.

GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins

Patel, K.

Lack of myostatin in mice results in excessive muscle but impaired force generation, tubular aggregates and alterations in fibre type profile

Paul, A.

Psychiatric symptoms as leading symptoms in patients with cerebellar tumors

Pavlidou, E.

Effectiveness of intermittent diazepam in febrile convulsions: A long term prospective controlled study

Pavlovic, J.

Cognitive functioning after stroke in childhood – a clinical study

Peirera, R.

Confirmation of the JBTS3 locus and identification of a new ahi1 gene mutation in Joubert syndrome (JS) type 3 with renal involvement – evidence for other JS-causing genes in this region?

Petek, E.

Breakage of the ERBB4-gene in a girl with reciprocal translocation t(1;2) (p22.3;q34) – Is there a relation to severe infantile epilepsy?

Petersen, D.

Rapid onset of cortical hemiatrophy and hippocampal sclerosis after prolonged febrile seizure
Encephalomyelitis disseminata in a child with severe outcome and atypical clinical findings – Neuromyelitis optica Devic or multiple sclerosis?

Pfander, T.

TorsinA and B expression in the brain is detectable in human infants as young as four weeks old

Philippi, H.

Patterns of infantile postural asymmetry: A standardized video-based analysis

Pieper, T.

Neuropathological spectrum of focal cortical dysplasia in children with severe focal epilepsies

Pietz, J.

The development of low-risk preterm infants from infancy to early adulthood

Plattner, B.

Behavior problems in patients with juvenile myoclonic epilepsy (JME)

Plecko, B.

Breakage of the ERBB4-gene in a girl with reciprocal translocation t(1;2) (p22.3;q34) – Is there a relation to severe infantile epilepsy?
Neuropsychiatric manifestations in juvenile systemic lupus erythematodes
Severe autoimmune chorea with positive antibasalganglia antibodies (ABGA) following herpesencephalitis: Treatment with plasmapheresis and corticosteroids
MASA (mental retardation, aphasia, shuffling gait, adducted thumbs): Intronic mutation of L1CAM gene in male twins
Cooper concentration of liver tissue under cooper histidin therapy in a patient with Menkes disease

Poggenburg, I.

Tuberculous meningitis with thalamus infarction
Parry-Romberg syndrome with focal epilepsy, progressive cerebral MRI alterations and CSF findings of a chronic inflammatory CNS disorder

Pohl, D.

'Immigrant-Ricketts' – an important differential diagnosis in neonatal seizures
Association of Epstein-Barr virus (EBV) infection with multiple sclerosis in pediatric patients

Pohl, M.

Confirmation of the JBTS3 locus and identification of a new ahi1 gene mutation in Joubert syndrome (JS) type 3 with renal involvement – evidence for other JS-causing genes in this region?

Porto, L.

Congenital spinal epidermoid cyst presenting as abscess of the spinal cord

Pöschl, J.

Decompressive craniectomy and duraplasty in severe bacterial encephalitis

Potschka, H.

Molecular and biochemical mechanisms of pharmacoresistance