DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 05 · Volume 32 · Oktober 2001 DOI: 10.1055/s-002-1321

Original Article

225
Raininko, R.; Thelin, L.; Eeg-Olofsson, O.: Non-Neoplastic Brain Abnormalities on MRI in Children and Adolescents with Neurofibromatosis Type 1
231
Saito, Y.; Oguni, H.; Awaya, Y.; Hayashi, K.; Osawa, M.: Phenytoin-Induced Choreoathetosis in Patients with Severe Myoclonic Epilepsy in Infancy
236
Kobayashi, K.; Ohtsuka, Y.; Ohno, S.; Ohmori, I.; Ogino, T.; Yoshinaga, H.; Tanaka, A.; Hiraki, Y.; Oka, E.: Clinical Spectrum of Epileptic Spasms Associated with Cortical Malformation
245
Okumura, A.; Watanabe, K.; Hayakawa, F.; Kato, T.: The Timing of Brain Insults in Preterm Infants Who Later Developed West Syndrome
250
Angelini, L.; Pietrogrande, M. C.; Delle Piane, M. R.; Zibordi, F.; Cinque, P.; Maccagnano, C.; Vago, L.: Progressive Multifocal Leukoencephalopathy in a Child with Hyperimmunoglobulin E Recurrent Infection Syndrome and Review of the Literature

Orginal Article

256
Ross, M. E.; Swanson, K.; Dobyns, W. B.: Lissencephaly with Cerebellar Hypoplasia (LCH): A Heterogeneous Group of Cortical Malformations

Short Communication

264
Holtmann, M.; Woermann, F. G.; Boenigk †, H. E.: Multiple Pterygium Syndrome, Bilateral Periventricular Nodular Heterotopia and Epileptic Seizures - a Syndrome?
267
Buxmann, H.; Schlösser, R.; Schlote, W.; Sewell, A.; Nowak, K. J.; Laing, N. G.; Loewenich, V. v: Congenital Nemaline Myopathy due to ACTA1-Gene Mutation and Carnitine Insufficiency: A Case Report
271
Wohlrab, Gabriele; Boltshauser, E.; Schmitt, B.: Neurological Outcome in Comatose Children with Bilateral Loss of Cortical Somatosensory Evoked Potentials

Letter to the Editor

275
Scherer, A.; Messing-Jünger, A. M.; Lackmann, G.-M.: Cleidocranial Dysostosis, Unilateral Sensorineural Hearing Loss and Gait Disturbances: A Clear-Cut Case of Diagnostic Mimicry?