Neuropediatrics
Issue 05 · October 2001
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Original Article
225
Raininko, R.; Thelin, L.; Eeg-Olofsson, O.:
Non-Neoplastic Brain Abnormalities on MRI in Children and Adolescents with Neurofibromatosis Type 1
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231
Saito, Y.; Oguni, H.; Awaya, Y.; Hayashi, K.; Osawa, M.:
Phenytoin-Induced Choreoathetosis in Patients with Severe Myoclonic Epilepsy in Infancy
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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
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245
Okumura, A.; Watanabe, K.; Hayakawa, F.; Kato, T.:
The Timing of Brain Insults in Preterm Infants Who Later Developed West Syndrome
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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
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Orginal Article
256
Ross, M. E.; Swanson, K.; Dobyns, W. B.:
Lissencephaly with Cerebellar Hypoplasia (LCH): A Heterogeneous Group of Cortical Malformations
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Short Communication
264
Holtmann, M.; Woermann, F. G.; Boenigk †, H. E.:
Multiple Pterygium Syndrome, Bilateral Periventricular Nodular Heterotopia and Epileptic Seizures - a Syndrome?
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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
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271
Wohlrab, Gabriele; Boltshauser, E.; Schmitt, B.:
Neurological Outcome in Comatose Children with Bilateral Loss of Cortical Somatosensory Evoked Potentials
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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?
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