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Organisation >> Universitätsklinikum Schleswig-Holstein (UK-SH), Campus Kiel >>

Klinik für Neonatologie, Kinderpneumologie und Neuropädiatrie

	2007 Flexible and floating choroid plexus cyst of the third ventricle: an ultrasonographic video documentation Spreading photoparoxysmal EEG response is associated with an abnormal cortical excitability pattern
	2006 A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27. A single dose of sulthiame induces a selective increase in resting motor threshold in human motor cortex: A transcranial magnetic stimulation study Antibiotic therapy for preterm premature rupture of membranes - results of a multicenter study. Association of BRD2 polymorphisms with photoparoxysmal response Candidate gene analysis of the succinic semialdehyde dehydrogenase gene (ALDH5A1) in patients with idiopathic generalized epilepsy and photosensitivity. Confirmation Of Tuberous Sclerosis Complex By High-resolution Ultrasonography Exploration of the genetic architecture of idiopathic generalized epilepsies Genetic analysis of the LGI/Epitempin gene family in sporadic and familial lateral temporal lobe epilepsy. Infant with unusually large choroid plexus papilloma undergoing emergency surgery. Case report with special emphasis on the surgical strategy Infectious mononucleosis and unilateral tongue writhing Neurophysiological reactivity before a migraine attack. Nichthamorrhagische subependymale Pseudozysten: sonographische=[Non-haemorrhagic Subependymal Pseudocysts: Ultrasonographic, Histological] Nonparalytic polyomyelitis in Lyme borreliosis Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy Relationship between precipitating agents and neurophysiological abnormalities in migraine Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome. Satoyoshi syndrome: a rare multisystemic disorder requiring systemic and symptomatic treatment The Spectrum from BCECTS to LKS: The Rolandic EEG Trait-Impact on Cognition
	2005 Are migraineurs hypersensitive? A test of the stimulus processing disorder hypothesis Das Schulungsprogramm FAMOSES und erste Ergebnisse Detection and characterization of changes of the correlation structure in multivariate time series. Evaluation des Schulungsprogramms FAMOSES Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Kortikale Reorganisation bei Kindern mit konnataler spastischer Hemiparese - eine funktionelle Magnetresonanztomographie-(fMRT-)Studie Leukoencephalopathy with ataxia, hypodontia, and hypomyelination Living a normal life with the nondominant hemisphere: magnetic resonance imaging findings and clinical outcome for a patient with left-hemispheric hydranencephaly Muscle fibre type grouping in high resolution ultrasound. Optimierung der Epilepsietherapie von Kindern und Jugendlichen mit Lamotrigin = [Optimizing Epilepsy Therapy in Children and Adolescents with Lamotrigine] Photosensitivity: genetics and clinical significance Prenatal diagnosis of isolated foramen ovale obstruction. A report of two cases SCN1A Mutation Analysis in Myoclonic Astatic Epilepsy and Severe Idiopathic Generalized Epilepsy of Infancy with Generalized Tonic-Clonic Seizures Zerebrale Anfälle beim Neugeborenen
	2004 [Neonatal chylothorax with trisomy 21] Benign Familial Infantile Convulsions: Linkage to Chromosome 16p12-q12 in 14 Families. Benigne Partialepilepsie des Kleinkindalters (Watanabe) : Definitionskriterien und genetische Aspekte. Choroid plexus cyst: comparison of new ultrasound technique with old histological finding. Genetics of Photosensitivity (Photoparoxysmal Response): A Review Induction of epileptic negative myoclonus by oxcarbazepine in symptomatic epilepsy. Labor- und Blutspiegelkontrollen bei antiepileptischer Behandlung von Kindern – Notwendigkeit oder Unsinn Lassen sich hyperkinetische Auffälligkeiten am Nachmittag durch eine Morgengabe von Methylphenidat Retard vermindern? = [Does a morning dose of Methylphenidate Retard reduce hyperkinetic symptoms in the afternoon?] Schreiunruhe, Rumpfasymmetrie, familiäre Obstipation und Infektionsanfälligkeit
	2003 Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families. Cerebral proton magnetic resonance spectroscopy in infantile Alexander disease. Grip force parameters in precision grip of individuals with myelomeningocele. ILAE Commission of European Affairs Subcommission on European Guidelines 1998-2001: The provision of epilepsy care across Europe. Migraine and asthma in childhood: evidence for specific asymmetric parent-child interactions in migraine and asthma families. Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects. Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patients. What kind of habituation is impaired in migraine patients?
	2002 A novel recessive hyperekplexia allele GLRA1 (S231R): genotyping by MALDI-TOF mass spectrometry and functional characterisation as a determinant of cellular glycine receptor trafficking. Clinical spectrum and genetics of Rolandic epilepsy. Detection of acute cytotoxic changes in progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome) using diffusion-weighted MRI and MR spectroscopy. Guidelines for the use of EEG methodology in the diagnosis of epilepsy. International League Against Epilepsy: commission report. Commission on European Affairs: Subcommission on European Guidelines. Hybrid nonlinear filtering approach to removing anharmonic periodic components from EEG time series. Infantile Alexander disease: a GFAP mutation in monozygotic twins and novel mutations in two other patients. Occipital sharp waves in idiopathic partial epilepsies--clinical and genetic aspects. Slow cortical potentials in migraine families are associated with psychosocial factors. Sonographic imaging of foramen ovale electrodes.
	2001 Atypical "benign" partial epilepsy or pseudo-Lennox syndrome. Part I: symptomatology and long-term prognosis.
	2000 Atypical benign partial epilepsy/pseudo-Lennox syndrome. Inheritance of photosensitivity. Migraine in childhood--are periodically occurring migraine attacks related to dynamic changes of cortical information processing? Neuropsychological long-term outcome of rolandic EEG traits. Paraneoplastic cerebellar degeneration in pediatric Hodgkin disease. The concept of hereditary impairment of brain maturation. The genetics of rolandic epilepsy. Typical semiology of benign childhood epilepsy with centrotemporal spikes (BCECTS).
	1999 [Anticonvulsant drug therapy in children and adults. Practical guide for single and multiple dosage] Benign idiopathic partial epilepsy and brain lesion. Migraine--evidence for a disturbance of cerebral maturation in man?
	1998 Centrotemporal spikes in families with rolandic epilepsy: linkage to chromosome 15q14. Neuroborreliosis and isolated trochlear palsy.
	1997 Benign childhood epilepsy with centrotemporal spikes and electroencephalography trait are not linked to EBN1 and EBN2 of benign neonatal familial convulsions. Clinical implications of maximal respiratory pressure determinations for individuals with Duchenne muscular dystrophy. Genetic EEG Traits in the Pathogenesis of the Epilepsies.
	1992 Myoclonic-astatic epilepsy. The different patterns of the photoparoxysmal response--a genetic study.
	1991 A genetically determined basic mechanism in benign partial epilepsies and related non-convulsive conditions.
	1989 Benign partial epilepsy and related conditions: multifactorial pathogenesis with hereditary impairment of brain maturation. Symptomatology in children with focal sharp waves of genetic origin.



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