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Abstracts of the 31st Annual Meeting of the Society for Neuropediatrics (Gesellschaft für Neuropädiatrie)
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Das, A. M.
Schimke immuno osseous dysplasia: pathophysiological investigations
Cerebral imaging of CNS involvement in haemolytic uraemic syndrome
Debus, J.
Paraneoplastic stiff-person syndrome in a girl with a petrous bone chondrosarcoma
Debus, O.
West syndrome in identical twins with white spots
Congenital disorders of glycosylation – a second patient of CDG type Id deficiency: different clinical phenotype, molecular analysis and prenatal diagnosis
Odontoid fracture after fall and following manipulation of the cervical spine – a case report -
Age of menarche in girls with epilepsy and antiepileptic therapy
Oral melatonin is a good medication for sleep induction for sleep eeg in children
Pyridoxal phosphat (vitamine B6) responsive West syndrome – follow up over 12 years
Sulthiame in childhood epilepsy
Paraneoplastic stiff-person syndrome in a girl with a petrous bone chondrosarcoma
De Jonghe, P.
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?
Denecke, J.
Congenital disorders of glycosylation – a second patient of CDG type Id deficiency: different clinical phenotype, molecular analysis and prenatal diagnosis
Denk, H.
Cooper concentration of liver tissue under cooper histidin therapy in a patient with Menkes disease
Deußen, L.
Protein S-100B as a serum marker of brain damage in paediatric brain injury
Deutsch, J.
Cooper concentration of liver tissue under cooper histidin therapy in a patient with Menkes disease
De Vivo, D. C.
GLUT-1 deficiency syndrome with ataxia, acquired microcephaly and leukoencephalopathy in monozygotic twins
Diers, A.
Spastic paraparesis caused by cerebrovascular neuroborreliosis in a 13-year-old boy
Distelmaier, F.
Isoniazid intoxication clinically mimicking encephalitis with status epilepticus
Dittrich, 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
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
Döhlemann, C.
Neurological and psychiatric symptoms due to mercury intoxication in a family from Iraq
Donnerstag, F.
Cerebral imaging of CNS involvement in haemolytic uraemic syndrome
Dötsch, J.
Hypoxia-inducible factor 1 (HIF-1)-regulated vasoactive factors in rat brain: gene expression in relation to the degree of global hypoxia in vivo
Drasch, G.
Neurological and psychiatric symptoms due to mercury intoxication in a family from Iraq
Drechsler, M.
Clinical and molecular features of a boy with incomplete WAGR syndrome and succinic semialdehyde dehydrogenase deficiency
Dumitrescu, A.
X-linked paroxysmal dyskinesia and severe global retardation caused by defective thyroid hormone transporter MCT8
Dumontier, J.
Cardiac and motor improvement with enzyme replacement therapy in a patient with infantile-onset Pompe disease