DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 36 · October 2005 DOI: 10.1055/s-002-4402

Review Article

285
Hoffmann, B.; Mayatepek, E.: Neurological Manifestations in Lysosomal Storage Disorders - From Pathology to First Therapeutic Possibilities

Original Article

290
Dinopoulos, A.; Cecil, K. M.; Schapiro, M. B.; Papadimitriou, A.; Hadjigeorgiou, G. M.; Wong, B.; deGrauw, T.; Egelhoff, J. C.: Brain MRI and Proton MRS Findings in Infants and Children with Respiratory Chain Defects
302
Klepper, J.; Scheffer, H.; Leiendecker, B.; Gertsen, E.; Binder, S.; Leferink, M.; Hertzberg, C.; Näke, A.; Voit, T.; Willemsen, M. A.: Seizure Control and Acceptance of the Ketogenic Diet in GLUT1 Deficiency Syndrome: A 2- to 5-Year Follow-Up of 15 Children Enrolled Prospectively
309
Bertini, E.; Donati, M. A.; Broda, P.; Cassandrini, D.; Petrini, S.; Dionisi-Vici, C.; Ballerini, L.; Boldrini, R.; D'Amico, A.; Pasquini, E.; Minetti, C.; Santorelli, F. M.; Bruno, C.: Phenotypic Heterogeneity in Two Unrelated Danon Patients Associated with the Same LAMP‐2 Gene Mutation
314
Moslemi, A.-R.; Darin, N.; Tulinius, M.; Oldfors, A.; Holme, E.: Two New Mutations in the MTATP6 Gene Associated with Leigh Syndrome
319
Kyllerman, M.; Rosengren, L.; Wiklund, L.-M.; Holmberg, E.: Increased Levels of GFAP in the Cerebrospinal Fluid in Three Subtypes of Genetically Confirmed Alexander Disease

Short Communication

324
Thijs, R. D.; Hazekamp, M. G.; Rijlaarsdam, M. E.; Willems, S. M.; Schutte, P. J.; Laan, L. A. E. M.: An Unexpected Cause of a Recurrent Cerebral Hemorrhage
328
Toelle, S. P.; Huisman, T. A. G. M.; Martin, E.; Boltshauser, E.: Marchiafava-Bignami-Like Injury of the Corpus Callosum in an Infant
332
Steiß, J. O.; Groß, S.; Neubauer, B. A.; Hahn, A.: Late-Onset Nephrotic Syndrome and Severe Cerebellar Atrophy in Galloway-Mowat Syndrome
336
Yalcinkaya, C.; Benbir, G.; Salomons, G. S.; Karaarslan, E.; Rolland, M. O.; Jakobs, C.; van der Knaap, M. S.: Atypical MRI Findings in Canavan Disease: A Patient with a Mild Course