DOI : 10.1055/s-00000041

Neuropediatrics

Issue 06 · Volume 37 · December 2006 DOI: 10.1055/s-002-5747


Abstracts of the 33rd Annual Meeting – of the Society of Neuropediatrics – (Gesellschaft für Neuropädiatrie)
Passau, 22 to 25 March 2007

F. Staudt, Passau
Abstracts (HTML) List of Authors
P81
Kornbrust, A.; Sassen, R.; Schramm, J.; Schorle, H.; Bartmann, P.; Heep, A.: Hemimegalencephaly – long-term follow up after functional hemispherectomy
P82
Brocke, K. S.; Kaindl, A. M.; Kress, W.; Stoltenburg-Dindinger, G.; Huebner, A.; Hahn, G.; Hagen, M. von der: Magnetic resonance imaging of skeletal muscles reveals a distinct pattern of muscle involvement in a family with congenital myopathy caused by a RYR1 mutation
P83
Müller, H. L.; Gebhardt, U.; Hunneman, D. H.; Stoffel-Wagner, B.; Reinehr, T.; Roth, C. L.: Reduced sympathetic metabolites in urine of obese patients with craniopharyngioma
P84
Gebhardt, U.; Handwerker, G.; Müller-Stöver, S.; Sörensen, N.; Müller, H. L.: Secondary narcolepsy may be a causative factor of increased daytime sleepiness in obese patients with childhood craniopharyngioma
P85
Vry, J.; Linder-Lucht, M.; Berweck, S.; Faist, M.; Mall, V.: Integrity of the corticospinal system in children with bilateral cerebral palsy and periventricular leukomalacia: A transcranial magnetic stimulation study
P86
Janzarik, W. G.; Kratz, C.; Pfister, S.; Loges, N. T.; Olbrich, H.; Klein, C.; Scheurlen, W.; Niemeyer, C.; Weiller, C.; Korinthenberg, R.; Omran, H.: Detection of a KRAS Mutation in a Pilocytic Astrocytoma
P87
Dreha-Kulaczewski, S.; Huppke, P.; Brockmann, K.; Dechent, P.; Helms, G.; Finsterbusch, J.; Frahm, J.; Gärtner, J.: Leukoencephalopathy with brain stem and spinal cord involvement and elevated white matter lactate (LBSL): Serial proton MRS and DTI of a child over a period of 6 years
P88
Johannsen, J.; Bentele, K. H. P.; Hasilik, M.; Hertzberg, C.; Mennicke, K.; Kruse, B.: Partial trisomy 5p and deletion of the 1p region causes severe psychomotor delay, refractory epilepsy and cleft lip and palate in a 10-year old girl – a long way to diagnosis
P89
Erhart, S.; Scholl-Bürgi, S.; Haberlandt, E.; Karall, D.; Albrecht, U.; Schmidt, A.; Amann, A.: 3-Heptanone in exhaled breath gas of patients with propionic acidemia and therapy with valproate
P90
Sanchez Albisua, I.; Lidzba, K.; Borell-Kost, S.; Mau-Holzmann, U.; Licht, P.; Krägeloh-Mann, I.: Developmental outcome of children conceived by ICSI at 5 years of age
P91
Geis, T.; Segerer, H.; Schilling, S.: Treatment failure in idiopathic intracranial hypertension in a male teenager
P92
Bernhard, M. K.; Seiffert, A.; Herbertz, S.; Merkenschlager, A.: Value and cost-benefit analysis of in-patient diagnosis of developmental retardation
P93
Bernhard, M. K.; Pomarino, D.; Mullik, A.; Herbertz, S.; Merkenschlager, A.: Does barefoot walking alter the manifestation of idiopathic toe walking? – Low prevalence among the children slum population of Dhaka (Bangladesh)
P94
Stülpnagel, C. von; Reilich, P.; Schäfer, J.; Blaschek, A.; Lee, S. H.; Henschel, V.; Mansmann, U.; Heinen, F.: Myofascial trigger points in children with tension-type headache: a new diagnostic and therapeutic option?
P95
Utzig, N.; Wagner, K.; Jagdhuhn, M.; Schröder, C.; Hirschfeld, H.; Hamm, A.; Lauffer, H.: Neurophysiological correlatives of eating behavior in obese children and adolescents
P96
Weber, P.; Hetzel, P.; Fahnenstich, H.; Lütschg, J.: Mismatch detection: an auditory event-related study to detect differences in pre-attentive and learning capability of fullterm and preterm newborns
P97
Bauer, A.; Püst, B.; Willig, B.: Monosymptomatic rheumatic fever – Chorea Sydenham
P98
Nüsken, E.; Plank, C.; Wenzel, D.; Trollmann, R.: Acute encephalopathy as the presenting symptom in Henoch-Schoenlein purpura: A case report
P99
Thimm, A.; Nies, H.; Köster, B.; Kaskel-Paul, S.; Rosenbaum, T.: Progressive hearing loss as presenting symptom of benign intracranial hypertension
P100
Neinert, J.; Fastnacht, E.; Larisch, R.; Legius, E.; Engelskirchen, R.; Messing-Juenger, M.; Reifenberger, G.; Rosenbaum, T.: Can 18FDG-PET detect malignant transformation of neurofibromas in patients with neurofibromatosis type I?
P101
Dittrich, S.; Hermann, E.; Boda, V.; Vlaho, S.; Qirshi, M.; Baz Bartels, M.; Gerlach, R.; Kieslich, M.: Bilateral decompressive craniectomy in a predominantly hypoxic brain damage
P102
Poretti, A.; Boltshauser, E.; Valente, E. M.; Huisman, T. A.: Failure of decussation of important pathways demonstrated by MR tractography in Joubert syndrome
P103
Nögel, S. C.; Andres, O.; Gempel, K.; Wenzel, D.; Trollmann, R.: 3-methylglutaconic aciduria in mitochondrial encepahlopathy: 2 case reports
P104
Hußmann, O.; Neubauer, B. A.; Hahn, A.: MRI- and neurophysiological findings in a case of Horizontal Gaze Palsy with Progressive Scoliosis (HGPPS)
P105
Poggenburg, I.; Marquardt, I.; Motz, R.; Hunneman, D. H.; Kutsche, K.; Korenke, G. C.: Elevated urine catecholamine metabolites: Indicating parameters for identification of Costello syndrome
P106
Pothmann, R.; Kremer, P.; Veelken, N.: Trigeminal neuralgia in children – differential therapy and neurosurgical indication
P107
Cirak, S.; Deimling, F. von; Wesley, E.; Herrmann, R.; Hoffmann, K.; Lindner, T.; Bönnemann, C.; Hinderlich, S.; Gil, P.; Peter, N.; Voit, T.: Ubiquitin-Proteasome pathway alteration in distal myopathy due to a mutation in a novel kelch protein
P108
Hahn, A.; Kafadar, I.; Stephani, U.; Neubauer, B. A.: Inspiratory muscle load during stenotic breathing in children with neuromuscular diseases
P109
Schäuble, B.; Wang, S.; Wiegand, F.; Hulihan, J.: Randomized dose-controlled multicenter study of topiramate as first line therapy in adolescents with epilepsy
P110
Weiss, C.; Weschke, B.; Uhlenberg, B.: Clinical manifestations and neuroimaging in neuroborreliosis – an unexpectedly high portion of patients with cerebral arteriopathy
P111
Thurner, B.; Spangenberg, P.; Kleines, M.; Blaum, M.; Häusler, M.: Successful continuous lumbar intrathecal interferon alpha treatment in SSPE
P112
Qirshi, M.; Dittrich, S.; Boda, V.; Baz Bartels, M.; Vlaho, S.; Kieslich, M.: Retrobulbar pain, diplopia and exophthalmus as manifestations of an isolated ocular myositis in a 15 year old boy
P113
Gerstl, J.; Hauch, H.; Tacke, J.; Friedrich, M.; Staudt, F.: Thickening of the dura mater T3-T9– incidental finding or manifestation of neuroborreliosis?
P114
Schallner, J.; Smitka, M.; Hahn, G.; Rohayem, J.; Hagen, M. von der; Ikonomidou, H.; Friebel, D.: Fulminant course of subacute sclerosing panencephalitis in an infant: electroencephalography as a guiding diagnostic instrument
P115
Janauschek, M.; Müller, S.; Villain, M.; Luthe, L.; Korenke, G. C.: Rare causes of hemicrania in childhood and youth
P116
Lütschg, J.; Haller, S.: Horizontal gaze palsy with progressive scoliosis
P117
Karenfort, M.; Heckel, M.; Assmann, B.; Tibussek, D.; Mayatepek, E.: Successfull therapy with Rituximab in an adolescent patient with severe multiple sclerosis
P118
Schulz, A.; Lukacs, Z.; Orth, U.; Gal, A.; Lebrun, A. H.; Kohlschütter, A.: Economical diagnosis of neuronal ceroid lipofuscinoses
P119
Schulz, A.; Kohlschütter, A.: The NCL-Net: How a network can improve care for patients with rare neurological diseases
P120
Scholl-Bürgi, S.; Haberlandt, E.; Heinz-Erian, P.; Albrecht, U.; Baumgartner Sigl, S.; Rauchenzauner, M.; Karall, D.: Urea cycle defects: Changes of amino acid CSF/plasma-ratios
P121
Stienen, A.; Kleines, M.; Dieckhöfer, A.; Scheithauer, S.; Häusler, M.: Neurological manifestations of EBV infection: a heterogeneous disease entity
P122
Lischetzki, G.; Lorenz, I.; Wenzel, D.: A cerebral sinus thrombosis in a 4 year old child
P123
Häusler, M.; Seiffert, P.; Cordes, J.; Kentrup, H.; Skopnik, H.; Merz, U.; Pascal, N.; Kleines, M.: Atypical presentations of herpes simplex virus encephalitis
P124
Vlaho, S.; Boda, V.; Baz Bartels, M.; Parbel, S.; Dittrich, S.; Lehrnbecher, T.; Porto, L.; Kieslich, M.: Posterior Reversible Encephalopathy Syndrome (PRES) in children – a single-institution retrosprective study
P125
Weiss, S.; Bittner, R. E.; Bernert, G.: Double Trouble: A clinical, molecular genetic mixed type of FSHD and Selenoprotein N rigid spine syndrome as a „new“ neuromuscular disease
P126
Hasilik, M.; Johannsen, J.; Fuchs, S.; Gal, A.; Bentele, K. H. P.; Kruse, B.: Ptosis, microcephaly and delayed motor development as main clinical manifestations in a female patient with chromosome 18p deletion-syndrome
P127
Cirak, S.; Herrmann, R.; Uyanik, G.; Lommel, M.; Albrecht, B.; Gross, C.; Strahl, S.; Voit, T.; Hehr, U.: Expanding the spectrum of POMT1 mutations: limb-girdle muscular dystrophy with mental retardation and microcephaly (LGMD2K)
P128
Debus, O.; Fiedler, B.; Schlegel, P.; Kurlemann, G.: Herpes Simplex Encephalitis: Progressive MRI-deterioration despite clinical stabilization with Acyclovir
P129
Kutschke, G.; Lampe, C.; Oberman, B.; Reitter, B.: Sensory motor neuropathy, myopathy, white matter abnormalities and lethal intestinal motility disturbance in a 15 years old boy – mitochondrial dysfunction due to thymidine phosphoryase deficiency
P130
Kleber, M.; Blankenburg, M.; Dietz, B.; Aksu, F.: Gait disturbance as a first sign of SSPE in early infancy
P131
Spiczak, S. von; Petersen, B.; Muhle, H.; Klein, C.; Stephani, U.: DYT11– Myoclonic Dystonia as a rare form of childhood dystonia