Neuropediatrics

Issue 05 · July 2004

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eFirst
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Publisher's Note
261
eFirst - Articles Published Ahead of Print

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Original Article
262
Messina, S.; Hartley, L.; Main, M.; Kinali, M.; Jungbluth, H.; Muntoni, F.; Mercuri, E.: Pilot Trial of Salbutamol in Central Core and Multi-Minicore Diseases

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267
Eiffert, H.; Karsten, A.; Schlott, T.; Ohlenbusch, A.; Laskawi, R.; Hoppert, M.; Christen, H.-J.: Acute Peripheral Facial Palsy in Lyme Disease - A Distal Neuritis at the Infection Site

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274
Ohto, T.; Iwasaki, N.; Fujiwara, J.; Ohkoshi, N.; Kimura, S.; Kawade, K.; Tanaka, R.; Matsui, A.: The Evaluation of Autonomic Nervous Function in a Patient with Hereditary Sensory and Autonomic Neuropathy Type IV with Novel Mutations of the TRKA Gene

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279
Oguz, K. K.; Anlar, B.; Senbil, N.; Cila, A.: Diffusion-Weighted Imaging Findings in Juvenile Metachromatic Leukodystrophy

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283
Leijser, L. M.; Klein, R. H.; Veen, S.; Liauw, L.; Van Wezel-Meijler, G.: Hyperechogenicity of the Thalamus and Basal Ganglia in Very Preterm Infants: Radiological Findings and Short-Term Neurological Outcome

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Short Communication
290
van der Heyden, J. J. C.; Verrips, A.; ter Laak, H. J.; Otten, B.; Fiselier, T.: Hypovitaminosis D-Related Myopathy in Immigrant Teenagers

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293
Kors, E. E.; Vanmolkot, K. R. J.; Haan, J.; Kheradmand Kia, S.; Stroink, H.; Laan, L. A. E. M.; Gill, D. S.; Pascual, J.; van den Maagdenberg, A. M. J. M.; Frants, R. R.; Ferrari, M. D.: Alternating Hemiplegia of Childhood: No Mutations in the Second Familial Hemiplegic Migraine Gene ATP1A2

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297
Del Bigio, M. R.; Chudley, A. E.; Booth, F. A.; Pacin, S.: Late Infantile Onset Krabbe Disease in Siblings with Cortical Degeneration and Absence of Cerebral Globoid Cells

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302
Lamont, P. J.; Thorburn, D. R.; Fabian, V.; Vajsar, J.; Hawkins, C.; Saada (Reisch), A.; Durling, H.; Laing, N. G.; Nevo, Y.: Nemaline Rods and Complex I Deficiency in Three Infants with Hypotonia, Motor Delay and Failure to Thrive

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307
Palmér, L.; Nordborg, C.; Steneryd, K.; Åman, P.; Kyllerman, M.: Large-Cell Medulloblastoma in Aicardi Syndrome. Case Report and Literature Review

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Kurian, M. A.; Hartley, L.; Zolkipli, Z.; Little, M. A.; Costigan, D.; Naughten, E. R.; Olpin, S.; Muntoni, F.; King, M. D.: Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with Early Onset Severe Axonal Neuropathy

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