DOI: 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 41 · February 2010 DOI: 10.1055/s-002-21148

Erratum

  • e2
    Herzer, M.; Koch, J.; Prokisch, H.; Rodenburg, R.; Rauscher, C.; Radauer, W.; Forstner, R.; Pilz, P.; Rolinski, B.; Freisinger, P.; Madignier, F.; Mayr, J. A.; Sperl, W.:

    Leigh Disease with Brainstem Involvement in Complex I Deficiency due to Assembly Factor NDUFAF2 Defect

  • Review Article

  • 1
    Gieselmann, V.; Krägeloh-Mann, I.:

    Metachromatic Leukodystrophy – An Update

  • Original Article

  • 7
    Pascual-Castroviejo, I.; Pascual-Pascual, S.I.; Velazquez-Fragua, R.; García-Guereta, L.; López-Gutiérrez, J.-C.; Olivares, P.; Tovar, J.:

    Association of Cutaneous Red-to-Purple Hemangiomas with Leptomeningeal Hemangiomas. A Clinical Study of Two Patients

  • 12
    Pinto, R. B.; Fröehlich, P. E.; Pitrez, E. H.; Bragatti, J. A.; Becker, J.; Cornely, A. F. H.; Schneider, A. C. R.; da Silveira, T. R.:

    MR Findings of the Brain in Children and Adolescents with Portal Hypertension and the Relationship with Blood Manganese Levels

  • 18
    Abdel-Salam, G. M. H.; El-Kamah, G. Y.; Rice, G. I.; EL-Darouti, M.; Gornall, H.; Szynkiewicz, M.; Aymard, F.; Zaki, M. S.; Abdel-Aleem, A. K.; Lebon, P.; Crow, Y. J.:

    Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome

  • 24
    Schaaf, H.; Pons-Kuehnemann, J.; Malik, C. Y.; Streckbein, P.; Preuss, M.; Howaldt, H.-P.; Wilbrand, J.-F.:

    Accuracy of Three-Dimensional Photogrammetric Images in Non-Synostotic Cranial Deformities

  • 30
    Herzer, M.; Koch, J.; Prokisch, H.; Rodenburg, R.; Rauscher, C.; Radauer, W.; Forstner, R.; Pilz, P.; Rolinski, B.; Freisinger, P.; Madignier, F.; Mayr, J. A.; Sperl, W.:

    Leigh Disease with Brainstem Involvement in Complex I Deficiency due to Assembly Factor NDUFAF2 Defect

  • Short Communication

  • 35
    Siri, L.; Battaglia, F. M.; Tessa, A.; Rossi, A.; Rocco, M. Di.; Facchinetti, S.; Mascaretti, M.; Santorelli, F. M.; Veneselli, E.; Biancheri, R.:

    Cognitive Profile in Spastic Paraplegia with Thin Corpus Callosum and Mutations in SPG11

  • 39
    Wakusawa, K.; Haginoya, K.; Ishitobi, M.; Hino-Fukuyo, N.; Togashi, N.; Sato, I.; Ohura, T.; Yokoyama, H.; Kikuchi, M.; Iinuma, K.; Tsuchiya, S.:

    The Cytokine and Chemokine Profiles in Rhabdomyolysis in a Patient with Gaucher Disease Type II

  • 43