DOI: 10.1055/s-00000041


Issue 05 · Volume 34 · October 2003 DOI: 10.1055/s-002-2901

Review Article

Wilke, M.; Holland, S. K.; Myseros, J. S.; Schmithorst, V. J.; Ball, W. S.: Functional Magnetic Resonance Imaging in Pediatrics

Original Article

Nakayama, J.; Hamano, K.; Iwasaki, N.; Ohta, M.; Nakahara, S.; Matsui, A.; Arinami, T.: Mutation Analysis of the Leucine-Rich, Glioma Inactivated 1 Gene (LGI1) in Japanese Febrile Seizure Patients
Wilken, B.; Dechent, P.; Brockmann, K.; Finsterbusch, J.; Baumann, M.; Ebell, W.; Korenke, G. C.; Pouwels, P. J. W.; Hanefeld, F. A.; Frahm, J.: Quantitative Proton Magnetic Resonance Spectroscopy of Children with Adrenoleukodystrophy Before and After Hematopoietic Stem Cell Transplantation
Kölker, S.; Hoffmann, G. F.; Schor, D. S. M.; Feyh, P.; Wagner, L.; Jeffrey, I.; Pourfarzam, M.; Okun, J. G.; Zschocke, J.; Baric, I.; Bain, M. D.; Jakobs, C.; Chalmers, R. A.: Glutaryl-CoA Dehydrogenase Deficiency: Region-Specific Analysis of Organic Acids and Acylcarnitines in post mortem Brain Predicts Vulnerability of the Putamen

Short Communication

Horstmann, M.; Neumaier-Probst, E.; Lukacs, Z.; Steinfeld, R.; Ullrich, K.; Kohlschütter, A.: Infantile Cobalamin Deficiency with Cerebral Lactate Accumulation and Sustained Choline Depletion
Desguerre, I.; Pinton, F.; Nabbout, R.; Moutard, M. L.; N'Guyen, S.; Marsac, C.; Ponsot, G.; Dulac, O.: Infantile Spasms with Basal Ganglia MRI Hypersignal May Reveal Mitochondrial Disorder Due to T8993G MT DNA Mutation
Horváth, J.; Ketelsen, U.-P.; Geibel-Zehender, A.; Boehm, N.; Olbrich, H.; Korinthenberg, R.; Omran, H.: Identification of a Novel LAMP2 Mutation Responsible for X-Chromosomal Dominant Danon Disease

Letter to the Editor

Auvin, S.; Cuvellier, J. C.; Vallée, L.: Isolated Recurrent Palatal Palsy in a Child