DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 38 · August 2007 DOI: 10.1055/s-002-8113

Original Article

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    Perretti, A.; Crispino, G.; Marcantonio, L.; Lenta, S.; Caropreso, M.; Manganelli, F.; Scianguetta, S.; Iorio, R.; Iolascon, A.; Vajro, P.:

    Clinical Utility of Electrophysiological Evaluation in Crigler-Najjar Syndrome

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    Ramaekers, V. T.; Sequeira, J. M.; Artuch, R.; Blau, N.; Temudo, T.; Ormazabal, A.; Pineda, M.; Aracil, A.; Roelens, F.; Laccone, F.; Quadros, E. V.:

    Folate Receptor Autoantibodies and Spinal Fluid 5-Methyltetrahydrofolate Deficiency in Rett Syndrome

  • 184
    Ramaekers, V. T.; Weis, J.; Sequeira, J. M.; Quadros, E. V.; Blau, N.:

    Mitochondrial Complex I Encephalomyopathy and Cerebral 5-Methyltetrahydrofolate Deficiency

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    Palmér, L.; Zetterlund, B.; Hård, A.-L.; Steneryd, K.; Kyllerman, M.:

    Aicardi Syndrome: Follow-Up Investigation of Swedish Children Born in 1975-2002

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    Bergqvist, A. G. C.; Schall, J. I.; Richard, E. L.; Gallagher, P. R.; Stallings, V. A.:

    Predictive Power of First Morning Glucose and the Ketogenic Diet

  • Short Communication

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    Hoffmann, F.; Reiter, K.; Kluger, G.; Holthausen, H.; Schwarz, H. P.; Borggraefe, I.; Bonfig, W.:

    Seizures, Psychosis and Coma: Severe Course of Hashimoto Encephalopathy in a Six-Year-Old Girl

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    Garavelli, L.; Guareschi, E.; Errico, S.; Simoni, A.; Bergonzini, P.; Zollino, M.; Gurrieri, F.; Mancini, G. M.; Schot, R.; Van Der Spek, P. J.; Frigieri, G.; Zonari, P.; Albertini, E.; Giustina, E. Della; Amarri, S.; Banchini, G.; Dobyns, W. B.; Neri, G.:

    Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus (MPPH): Report of a New Case

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    Beretta, L.; Hauschild, M.; Jeannet, P.-Y.; Addor, M.-C.; Maeder, P.; Truttmann, A. C.:

    Atypical Presentation of Prader-Willi Syndrome with Cerebral Venous Thrombosis: Association or Fortuity?

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    Giovanniello, T.; Leuzzi, V.; Carducci, C.; Sabato, M. L. Di; Artiola, C.; Santagata, S.; Pozzessere, S.; Antonozzi, I.:

    Tyrosine Hydroxylase Deficiency Presenting with a Biphasic Clinical Course