Neuropediatrics
Issue 05 · October 2005
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Review Article
285
Hoffmann, B.; Mayatepek, E.:
Neurological Manifestations in Lysosomal Storage Disorders - From Pathology to First Therapeutic Possibilities
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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
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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
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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
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314
Moslemi, A.-R.; Darin, N.; Tulinius, M.; Oldfors, A.; Holme, E.:
Two New Mutations in the
MTATP6
Gene Associated with Leigh Syndrome
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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
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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
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328
Toelle, S. P.; Huisman, T. A. G. M.; Martin, E.; Boltshauser, E.:
Marchiafava-Bignami-Like Injury of the Corpus Callosum in an Infant
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332
Steiß, J. O.; Groß, S.; Neubauer, B. A.; Hahn, A.:
Late-Onset Nephrotic Syndrome and Severe Cerebellar Atrophy in Galloway-Mowat Syndrome
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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
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