DOI : 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 43 · April 2012 DOI: 10.1055/s-002-23054


Abstracts of the 38th Annual Meeting of the Society of Neuropediatrics
Münster, 19th to 22nd April 2012

Chair: Prof. Dr. med. Gerhard Kurlemann, Münster
Abstracts (HTML) List of Authors
PS16_01
Laufs, M; Porto, L; Kieslich, M: Leucencephalopathy with intracranial calcifications and cysts as well as conjuctival and pharyngeal teleangiectasias: Labrune syndrome variant
PS16_02
Gruber-Sedlmayr, U; Brunner-Krainz, M; Müller, M; Zebedin, D; Sorantin, E: CT Perfusion and CT Angiography in children and juvenile patients during an attack of migraine with aura
PS16_03
Müller, M; Gruber-Sedlmayr, U; Zenz, W: Tick-borne encephalitis: four cases in young vaccinated children
PS16_04
Schleede, L; Weigt-Usinger, K; Smitka, M; Stephan, S; Baumgartner, S; Opladen, T; Kaiser, O; Lücke, T; Rostásy, K; van Baalen, A; Jorch, G; Schara, U; Skopnik, H; Häusler, M: Pediatric herpes simplex virus encephalitis: a critical multicentric analysis
PS16_05
Hennes, E; Rostásy, K; Zotter, S; Dorninger, L; Hartmann, H; Häusler, M; Huppke, P; Jacobs, J; Kraus, V; Schlachter, K; Ulmer, H; van Baalen, A; Koch, J: Long-term outcome and MRI findings in children with acute cerebellitis
PS16_06
Geis, T; Schilling, S; Hehr, U: Perinatal cerebral infarction due to incontinentia pigmenti
PS16_07
Rodemann, S; Bevot, A; Goelz, R; Krägeloh-Mann, I; Ranke, M: Relationship between growth and psychomotor development of preterm children
PS16_08
Neumann, H; Weitkämper, A; Weigt-Usinger, K; Schauer, U; Teig, N; Lücke, T: Neurocognitive testing of very low birth weight infants at an age of 4 years
PS16_09
Bigi, S; Makhani, N; Banwell, B: Hiccups, Vomiting and the Brain
PS16_10
Zirn, B; Arning, L; Bartels, I; Shoukier, M; Hoffjan, S; Neubauer, B; Hahn, A: Ring chromosome 22 and neurofibromatosis type II: proof of two hit model for the loss of the NF2 gene in the development of meningioma
PS16_12
Vietzke, D; Goecke, T; Distelmaier, F; Lohnstein, P; Kohlhase, J; Lohmeier, K; Karenfort, M; Mayatepek, E: Sudden bilateral sensorineural deafness in a 5 years old girl with blue sclerae, keratoconus, hypermobility of the joints and hyperelasticity of the skin with a mutation in the ZNF469 gene encoding for Brittle-Cornea-Syndrome