DOI: 10.1055/s-00000041

Neuropediatrics

Issue 01 · Volume 41 · February 2010 DOI: 10.1055/s-002-21148

Erratum

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Herzer, M.; Koch, J.; Prokisch, H.; Rodenburg, R.; Rauscher, C.; Radauer, W.; Forstner, R.; Pilz, P.; Rolinski, B.; Freisinger, P.; Madignier, F.; Mayr, J. A.; Sperl, W.: Leigh Disease with Brainstem Involvement in Complex I Deficiency due to Assembly Factor NDUFAF2 Defect

Review Article

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Gieselmann, V.; Krägeloh-Mann, I.: Metachromatic Leukodystrophy – An Update

Original Article

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Pascual-Castroviejo, I.; Pascual-Pascual, S.I.; Velazquez-Fragua, R.; García-Guereta, L.; López-Gutiérrez, J.-C.; Olivares, P.; Tovar, J.: Association of Cutaneous Red-to-Purple Hemangiomas with Leptomeningeal Hemangiomas. A Clinical Study of Two Patients
12
Pinto, R. B.; Fröehlich, P. E.; Pitrez, E. H.; Bragatti, J. A.; Becker, J.; Cornely, A. F. H.; Schneider, A. C. R.; da Silveira, T. R.: MR Findings of the Brain in Children and Adolescents with Portal Hypertension and the Relationship with Blood Manganese Levels
18
Abdel-Salam, G. M. H.; El-Kamah, G. Y.; Rice, G. I.; EL-Darouti, M.; Gornall, H.; Szynkiewicz, M.; Aymard, F.; Zaki, M. S.; Abdel-Aleem, A. K.; Lebon, P.; Crow, Y. J.: Chilblains as a Diagnostic Sign of Aicardi-Goutières Syndrome
24
Schaaf, H.; Pons-Kuehnemann, J.; Malik, C. Y.; Streckbein, P.; Preuss, M.; Howaldt, H.-P.; Wilbrand, J.-F.: Accuracy of Three-Dimensional Photogrammetric Images in Non-Synostotic Cranial Deformities
30
Herzer, M.; Koch, J.; Prokisch, H.; Rodenburg, R.; Rauscher, C.; Radauer, W.; Forstner, R.; Pilz, P.; Rolinski, B.; Freisinger, P.; Madignier, F.; Mayr, J. A.; Sperl, W.: Leigh Disease with Brainstem Involvement in Complex I Deficiency due to Assembly Factor NDUFAF2 Defect

Short Communication

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Siri, L.; Battaglia, F. M.; Tessa, A.; Rossi, A.; Rocco, M. Di.; Facchinetti, S.; Mascaretti, M.; Santorelli, F. M.; Veneselli, E.; Biancheri, R.: Cognitive Profile in Spastic Paraplegia with Thin Corpus Callosum and Mutations in SPG11
39
Wakusawa, K.; Haginoya, K.; Ishitobi, M.; Hino-Fukuyo, N.; Togashi, N.; Sato, I.; Ohura, T.; Yokoyama, H.; Kikuchi, M.; Iinuma, K.; Tsuchiya, S.: The Cytokine and Chemokine Profiles in Rhabdomyolysis in a Patient with Gaucher Disease Type II
43
Schessl, J.; Columbus, A.; Hu, Y.; Zou, Y.; Voit, T.; Goebel, H. H.; Bönnemann, C. G.: Familial Reducing Body Myopathy with Cytoplasmic Bodies and Rigid Spine Revisited: Identification of a Second LIM Domain Mutation in FHL1