DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 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