DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 35 · June 2004 DOI: 10.1055/s-002-3472

Original Article

151
Korman, S. H.; Salomons, G. S.; Gutman, A.; Brooks, R.; Jakobs, C.: D-2-Hydroxyglutaric Aciduria and Glutaric Aciduria Type 1 in Siblings: Coincidence, or Linked Disorders?
157
Hartmann, H.; Uyanik, G.; Gross, C.; Hehr, U.; Lücke, T.; Arslan-Kirchner, M.; Antosch, B.; Das, A. M.; Winkler, J.: Agenesis of the Corpus Callosum, Abnormal Genitalia and Intractable Epilepsy due to a Novel Familial Mutation in the Aristaless-Related Homeobox Gene
161
Kato, T.; Okumura, A.; Hayakawa, F.; Kuno, K.; Watanabe, K.: Electroencephalographic Aspects of Periventricular Hemorrhagic Infarction in Preterm Infants
167
Huck, J. H. J.; Verhoeven, N. M.; van Hagen, J. M.; Jakobs, C.; van der Knaap, M. S.: Clinical Presentations of Patients with Polyol Abnormalities
174
Rudnik-Schöneborn, S.; Stolz, P.; Varon, R.; Grohmann, K.; Schächtele, M.; Ketelsen, U.-P.; Stavrou, D.; Kurz, H.; Hübner, C.; Zerres, K.: Long-Term Observations of Patients with Infantile Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1)
183
Müller, J. S.; Petrova, S.; Kiefer, R.; Stucka, R.; König, C.; Baumeister, S. K.; Huebner, A.; Lochmüller, H.; Abicht, A.: Synaptic Congenital Myasthenic Syndrome in Three Patients due to a Novel Missense Mutation (T441A) of the COLQ Gene

Short Communication

190
Saltik, S.; Saip, S.; Kocer, N.; Siva, A.; Yalçinkaya, C.: MRI Findings in Pediatric Neuro-Behçet's Disease
194
Mohammadi, M.; Mohebbi, M. R.; Holden, K. R.: Facial Hemangioma, and Associated Malformations: A Case Report
198
Milani, N.; Zibordi, F.; Erbetta, A.; Pollo, B.; Angelini, L.: Neuromyelitis Optica in a Child with Atypical Onset and Severe Outcome
202
Hahn, A.; Gross, C.; Uyanik, G.; Hehr, U.; Hügens-Penzel, M.; Alzen, G.; Neubauer, B. A.: X-Linked Lissencephaly with Abnormal Genitalia Associated with Renal Phosphate Wasting