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Abstracts of the 31st Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)
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Gallistl, G.
Development of transcallosal inhibition after focal magnetic stimulation in children: a longitudinal study
Gärtner, J.
TorsinA and B expression in the brain is detectable in human infants as young as four weeks old
Highly skewed X-inactivation leading to an extremely mild variant of Rett syndrome with predominantly psychiatric problems
Functional consequence and clinical importance of distinct mutations in CLN2, the gene associated with classical late infantile ceroid lipofuscinosis
GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins
A pathognomonic MRI pattern can be the major clue to a peroxisomal disorder in case of pitfalls in metabolic screening
Psychiatric symptoms as leading symptoms in patients with cerebellar tumors
Hereditary spastic paraplegia with thin corpus callosum – childhood onset in two patients
Gassmann, M.
Excessive erythrocytosis and non-erythropoietic functions of erythropoietin
Gebhardt, B.
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
Protein S-100B as a serum marker of brain damage in paediatric brain injury
Recurrent isolated cranial nerve palsy associated with Mycoplasma pneumoniae infection
Congenital spinal epidermoid cyst presenting as abscess of the spinal cord
Increased CSF ratio of glutamine to branched chain amino acids in DOPA non responsive but gabapentin responsive dystonia
Gempel, K.
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
Gerlach, R.
Protein S-100B as a serum marker of brain damage in paediatric brain injury
Congenital spinal epidermoid cyst presenting as abscess of the spinal cord
Gerloff, C.
Hemispheric dissociation between motor and sensory hand representations in congenital hemiparesis: TMS, fMRI, MEG
Gilitzer, C.
Cardiac and motor improvement with enzyme replacement therapy in a patient with infantile-onset Pompe disease
Gillessen-Kaesbach, G.
Two unrelated patients with Nicolaides-Baraitser syndrome
Giovannoni, G.
Severe autoimmune chorea with positive antibasalganglia antibodies (ABGA) following herpesencephalitis: Treatment with plasmapheresis and corticosteroids
Gombakis, N.
Abnormal eye movements and photophobia in 2 siblings: achromatopsia type 2 due to mutation of the CNGA3 gene
Göpel, W.
The impact of genetic polymorphisms on the development of intraventricular haemorrhage, periventricular leucomalacia and hydrocephalus in very-low-birth-weight-infants
Granel, M.
Refractory status epilepticus after non-specific infection in 3 previously healthy children
Gratzki, N.
Aneurysm of the axillary artery in a child with tuberous sclerosis
Greess, H.
Peptic stricture of the esophagus in a patient with Cornelia de Lange syndrome, a typical complication
Greeß, H.
Aneurysm of the axillary artery in a child with tuberous sclerosis
Gresch, M.
Genomewide linkage scan of the photoparoxysmal response (PPR) and exploration of its relationship to Idiopathic Generalised Epilepsies (IGE)
Grodd, W.
Hemispheric dissociation between motor and sensory hand representations in congenital hemiparesis: TMS, fMRI, MEG
Presurgical motor fMRI in a 3-year-old child
Groeschel, S.
Age-related changes of cerebral white and grey matter structures from childhood to adulthood using voxel-based morphometry
Groninger, A.
Neurofibroma-derived Schwann cells hyperproliferate in response to progesterone
Gross, C.
Neonatal seizures, lissencephaly and abnormal genitalia – a case of XLAG-syndrome
Groß, D.
Patterns of infantile postural asymmetry: A standardized video-based analysis
Grubbauer, H. M.
Severe autoimmune chorea with positive antibasalganglia antibodies (ABGA) following herpesencephalitis: Treatment with plasmapheresis and corticosteroids
Gruber-Sedlmayr, U.
Neuropsychiatric manifestations in juvenile systemic lupus erythematodes
Severe autoimmune chorea with positive antibasalganglia antibodies (ABGA) following herpesencephalitis: Treatment with plasmapheresis and corticosteroids
Gutsche, S.
Possible central nervous graft-versus-host reaction after stem cell transplantation by chronic myeloid leukemia