DOI: 10.1055/s-00000041


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


Review Article

Original Article

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
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

Short Communication

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
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
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