DOI: 10.1055/s-00000041

Neuropediatrics

Issue 02 · Volume 37 · April 2006 DOI: 10.1055/s-002-4945

Original Article

59
Ölmez, A.; Uyanik, G.; Özgül, R. K.; Gross, C.; Cirak, S.; Elibol, B.; Anlar, B.; Winner, B.; Hehr, U.; Topaloglu, H.; Winkler, J.: Further Clinical and Genetic Characterization of SPG11: Hereditary Spastic Paraplegia with Thin Corpus Callosum
67
Havasi, V.; Komlósi, K.; Bene, J.; Melegh, B.: Increased Prevalence of Glycoprotein IIb/IIIa Leu33Pro Polymorphism in Term Infants with Grade I Intracranial Haemorrhage
72
Friebel, D.; von der Hagen, M.; Baumgartner, E. R.; Fowler, B.; Hahn, G.; Feyh, P.; Heubner, G.; Baumgartner, M. R.; Hoffmann, G. F.: The First Case of 3-Methylcrotonyl-CoA Carboxylase (MCC) Deficiency Responsive to Biotin
79
Nitschke, M. F.; Erdmann, C.; Trillenberg, P.; Sprenger, A.; Kock, N.; Sperner, J.; Klein, C.: Functional MRI Reveals Activation of a Subcortical Network in a 5-Year-Old Girl with Genetically Confirmed Myoclonus-Dystonia
83
Feenstra, I.; van Ravenswaaij, C. M. A.; van der Knaap, M. S.; Willemsen, M. A. A. P.: Neuroimaging in Nine Patients with Inversion Duplication of the Short Arm of Chromosome 8
88
van Riesen, A. K. J.; Antonicka, H.; Ohlenbusch, A.; Shoubridge, E. A.; Wilichowski, E. K. G.: Maternal Segmental Disomy in Leigh Syndrome with Cytochrome c Oxidase Deficiency Caused by Homozygous SURF1 Mutation

Short Communication

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Rosewich, H.; Waterham, H. R.; Wanders, R. J. A.; Ferdinandusse, S.; Henneke, M.; Hunneman, D.; Gärtner, J.: Pitfall in Metabolic Screening in a Patient with Fatal Peroxisomal β-Oxidation Defect
99
Hoving, M. A.; Smulders, N. M.; Abdul Fatah, B.; van Kroonenburgh, M. J. P. G.; van Raak, E. P. M.; Spincemaille, G. H. J. J.; Vles, J. S. H.: The Use of an Indium111 DTPA Flow Study in the Evaluation of a Lumbar Swelling in a Girl with a Baclofen Pump
102
Elzinga-Huttenga, J.; Hekster, Y.; Bijl, A.; Rotteveel, J.: Movement Disorders Induced by Gastrointestinal Drugs: Two Paediatric Cases
107
Parazzini, C.; Rossi, L.; Righini, A.; Bianchini, E.; Mastrangelo, M.; Spreafico, F.; Triulzi, F.: Spinal Cord and Vertebral Stroke: A Paediatric Case
110
Hourani, R. G.; Barada, W. M.; Al-Kutoubi, A. M.; Hourani, M. H.: Atypical MRI Findings in Kearns-Sayre Syndrome: T2 Radial Stripes