DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 36 · August 2005 DOI: 10.1055/s-002-4313

Editorial

  • 229

    Notice to the Authors and Readers of Neuropediatrics - Online Manuscript Submission in Preparation

    • Review Article

  • 230
    Rostásy, K. M.:

    Inflammation and Neuroaxonal Injury in Multiple Sclerosis and AIDS Dementia Complex: Implications for Neuroprotective Treatment

  • 240
    Oehmichen, M.; Meissner, C.; Saternus, K.-S.:

    Fall or Shaken: Traumatic Brain Injury in Children Caused by Falls or Abuse at Home - A Review on Biomechanics and Diagnosis

    • Original Article

  • 246
    Ketelsen, U.-P.; Brand-Saberi, B.; Uhlenberg, B.; Wagner, M.; Laberke, H.-G.; Omran, H.:

    Congenital Myopathy with Arrest of Myogenesis Prior to Formation of Myotubes

  • 252
    Tacke, U.; Olbrich, H.; Sass, J. O.; Fekete, A.; Horvath, J.; Ziyeh, S.; Kleijer, W. J.; Rolland, M.-O.; Fisher, S.; Payne, S.; Vargiami, E.; Zafeiriou, D. I.; Omran, H.:

    Possible Genotype-Phenotype Correlations in Children with Mild Clinical Course of Canavan Disease

  • 256
    Panetta, J.; Gibson, K.; Kirby, D. M.; Thorburn, D. R.; Boneh, A.:

    The Importance of Liver Biopsy in the Investigation of Possible Mitochondrial Respiratory Chain Disease

    • Short Communication

  • 260
    Rostásy, K. M.; Huppke, P.; Beckers, B.; Brockmann, K.; Degenhardt, V.; Wesche, B.; König, F.; Gärtner, J.:

    Acute Motor and Sensory Axonal Neuropathy (AMSAN) in a 15-Year-Old Boy Presenting with Severe Pain and Distal Muscle Weakness

  • 265
    Di Rocco, M.; Rossi, A.; Parenti, G.; Allegri, A. E. M.; Filocamo, M.; Pessagno, A.; Tortori-Donati, P.; Minetti, C.; Biancheri, R.:

    Different Molecular Mechanisms Leading to White Matter Hypomyelination in Infantile Onset Lysosomal Disorders

  • 270
    Barone, R.; Lempereur, L.; Anastasi, M.; Parano, E.; Pavone, P.:

    Congenital Insensitivity to Pain with Anhidrosis (NTRK1 Mutation) and Early Onset Renal Disease: Clinical Report on Three Sibs with a 25-Year Follow-Up in One of Them

  • 274
    Brockmann, K.; Simpson, M. A.; Faber, A.; Bönnemann, C.; Crosby, A. H.; Gärtner, J.:

    Complicated Hereditary Spastic Paraplegia with Thin Corpus Callosum (HSP‐TCC) and Childhood Onset

  • 279
    Pavone, P.; Incorpora, G.; Ruggieri, M.:

    A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies