DOI : 10.1055/s-00000041

Neuropediatrics

Ausgabe 02 · Volume 44 · März 2013 DOI: 10.1055/s-003-24657


Abstracts of the 39th Annual Meeting of the Society of Neuropediatrics
Innsbruck, 25th to 28th April 2013

Chair: PD Dr. Kevin Rostásy, Kinderklinik Innsbruck, Medizinische Universität Innsbruck
Abstracts (HTML) Autorenliste
PS21_1043
Poretti, A; Meoded, A; Huisman, TAGM: Maturation of the brainstem and cerebellar white matter tracts from the neonatal period to adolescence: a diffusion tensor imaging study
PS21_1030
Poretti, A; Rostásy, K; Wei, XC; Fauth, C; Koch, J; Hader, WJ; Valente, EM; Huisman, TAGM; Boltshauser, E: Tectocerebellar dysraphism with occipital encephalocele is part of the Joubert syndrome spectrum
PS21_1031
Bosemani, T; Boltshauser, E; Staudt, M; Flores-Sarnat, L; Bürki, S; Pieper, T; Sarnat, HB; Wei, XC; Hartman, AL; Huisman, TAGM; Poretti, A: Hemimegalencephaly: involvement of cranial nerves and intracranial vessels
PS21_1036
Messmer, C; Zirn, S; Schuster, M: Central or combined central and peripheral hearing loss at an early born child
PS21_1113
Albers, K; Jung, C; Asmussen, M; Prietsch, V: Jacobsen syndrome: a rare differential diagnosis of multifocal white matter lesions
PS21_1137
Walsh, S; Schallner, J; Freudenberg, L; Smitka, M; der Hagen, M von; Warmuth-Metz, M; Hahn, G: Hypertrophic olivary degeneration: a differential diagnosis to consider following surgical intervention in the posterior cranial fossa: review and two case reports
PS21_1162
Eisenkölbl, A; Rossegg, U; Biebl, A; Schwarz, R; Weissensteiner, M; Wiesinger-Eidenberger, G: Kernicterus: a case study
PS21_1181
Knotz, J; Porto, L; Kieslich, M: Atypical case of a neurocutaneous melanosis with typical magnetic resonance imaging findings
PS21_1243
Siegel, C; Haack, TB; Makowski, C; Tauer, U; Oexle, K; Walther, A; Wieland, T; Meitinger, T; Strom, TM; Prokisch, H; Hempel, M: Band-like calcification with simplified gyration and polymicrogyria: further delineation of phenotype and review of literature
PS21_1268
Elpers, C; Fiedler, B; Schwindt, W; Henkes, H; Omran, H; Stummer, W; Kurlemann, G: Rare cause of oculomotor palsy