DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 01 · Volume 42 · Februar 2011 DOI: 10.1055/s-002-21992

Rapid Communication

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Vermeulen, R. J.; Peeters-Scholte, C.; Van Vugt, J. J. M. G.; Barkhof, F.; Rizzu, P.; van der Schoor, S. R. D.; van der Knaap, M. S.: Fetal Origin of Brain Damage in 2 Infants with a COL4A1 Mutation: Fetal and Neonatal MRI

Original Article

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Gosk, J.; Koszewicz, M.; Urban, M.; Wnukiewicz, W.; Wiace, R.; Rutowski, R.: Assessment of the Prognostic Value of Horner Syndrome in Perinatal Brachial Plexus Palsy
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Kornek, B.; Bernert, G.; Rostasy, K.; Mlczoch, E.; Feucht, M.; Prayer, D.; Vass, K.; Seidl, R.: Long-Term Follow-Up of Pediatric Patients Treated with Mitoxantrone for Multiple Sclerosis
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van Maldegem, B. T.; Kloosterman, S. F.; Janssen, W. J.; Augustijn, P. B.; van der Lee, J. H.; IJlst, L.; Waterham, H. R.; Duran, R.; Wanders, R. J. A.; Wijburg, F. A.: High Prevalence of Short-Chain Acyl-CoA Dehydrogenase Deficiency in the Netherlands, but No Association with Epilepsy of Unknown Origin in Childhood
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Jung, N. H.; Heinen, F.; Westhoff, B.; Doederlein, L.; Reissig, A.; Berweck, S.; Linder-Lucht, M.; Schandelmaier, S.; Mall, V.: Hip Lateralisation in Children with Bilateral Spastic Cerebral Palsy Treated with Botulinum Toxin Type A: A 2-Year Follow-Up

Short Communications

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Pascual-Castroviejo, I.; Parrón Pajares, M.; Pascual-Pascual, S.-I.; Jara, P.; Velázquez-Fragua, R.: Cutaneous, Mediastinal and Hepatic Hemangiomas in a Girl Followed During 12 Years

Short Communication

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Häusler, M.; Kluger, G.; Nikanorova, M.: Epilepsy with Myoclonic Absences – Favourable Response to Add-on Rufinamide Treatment in 3 Cases
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Porfirio, M. C.; Giana, G.; Giovinazzo, S.; Curatolo, P.: Methylphenidate-Induced Visual Hallucinations
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Kulkarni, K. S.; Baranano, K. W.; Lin, D. D. M.; Raymond, G. V.: Contrast Enhancement of Brainstem Tracts in Zellweger Spectrum Disorder: Evidence of Inflammatory Demyelination?
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Saleem, S. N.; Zaki, M. S.; Soliman, N. A.; Momtaz, M.: Prenatal Magnetic Resonance Imaging Diagnosis of Molar Tooth Sign at 17 to 18 Weeks of Gestation in Two Fetuses at Risk for Joubert Syndrome and Related Cerebellar Disorders