Abstracts of the 37th Annual Meeting of the Society of Neuropediatrics

Abstracts (HTML) List of Authors

Faber, J

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Feldkamp, A

Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Feucht, M

Use of the ketogenic diet in drug resistant epilepsy syndromes during early infancy: Differences between 3: 1 and 4: 1 formula, a pilot study

Fiedler, B

Differenzial diagnosis of acute encephalopathy: Acute decompensation in ornithine transcarbamylase (OTC) deficiency in a seven year old girl
Hereditary sensory and autonomic neuropathy Type IV – a case report with detection of two previously unknown sequence variants in NTKR1 gene

Fiedler, BJ

Potocki-Shaffer Syndrome: A case study

Finetti, C

Spine fracture following generalized tonic-clonic seizures in a 16 years old girl. An unusual case
Complete occlusion of the left internal carotid artery in neurofibromatosis type 1. Congenital dysplasia or progressive occlusion?

Fingerhut, M

Status epilepticus in a newborn – pyridoxine toxicity?

Fleischer, J

Constraint-induced movement therapy versus bimanual therapy for children with central hemiparesis – relative effectiveness and factors of influence

Flössel, U

A case of sudden cardiac death in a patient with LPIN1 gene mutation

Forne, I

Anti-MOG autoantibodies in children with acute demyelination: Comparison of assays and longitudinal analysis

Fowler, B

Infantile epileptic encephalopathy due to cobalamin deficiency?
Comparing two children with different inborn errors of remethylation: Classic and unusual clinical presentation, diagnosis, MRI changes and outcome under treatment with betaine, cobalamin, folate and carnitine

Franke, C

Treatment of severe childhood Multiple Sclerosis with plasmapheresis

Frauenknecht, K

Isolated, monocular vertical nystagmus: single symptom of an extensive intracerebral tumor

Freilinger, M

Early plasmapheresis in 3 consecutive cases of choreo-athetotic movement disorder after HSV-1 encephalitis

Freisinger, P

Long-term outcome of children with cytochrome-C-oxidase-deficiency and SURF-1-mutation
Deficiency of the mitochondrial phosphate carrier as a cause of combined mitochondrial (cardio-)myopathy
Biochemical and genetic testing in a large cohort of patients with suspicion of mitochondriopathy
Progressive dyskinetic spastic paresis in siblings: a new disorder of pyruvate oxidation
Mitochondrial complex I deficiency: exome sequencing aids efficient diagnosis and identification of a novel disease gene
Mitochondrial complex I deficiency – new diagnostic approaches allow better genetic characterisation of 150 patients

Freudenberg, L

A four day course of Lovastatin improves synaptic plasticity in patients with NF-1