DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 42 · August 2011 DOI: 10.1055/s-002-22311

Review Article

129
Jahn, K.; Langhagen, T.; Schroeder, A.S.; Heinen, F.: Vertigo and Dizziness in Childhood − Update on Diagnosis and Treatment

Original Article

135
Yamashita, S.; Okumura, A.; Yamamoto, T.; Shimojima, K.; Tanabe, T.; Shimizu, T.: SCN1B is Not Related to Benign Partial Epilepsy in Infancy or Convulsions with Gastroenteritis
138
Ortibus, E.; Laenen, A.; Verhoeven, J.; De Cock, P.; Casteels, I.; Schoolmeesters, B.; Buyck, A.; Lagae, L.: Screening for Cerebral Visual Impairment: Value of a CVI Questionnaire

Short Communication

148
Hahn, A.; Schänzer, A.; Neubauer, B.A.; Gizewski, E.; Ahting, U.; Rolinski, B.: MERRF-Like Phenotype Associated with a Rare Mitochondrial tRNAIle Mutation (m.4284 G>A)
152
Cuppen, I.; Vinck, A.; Geerdink, N.; Rotteveel, J. J.; Roeleveld, N.; Pasman, J. W.: Early Infantile Electroencephalography in Patients with Spina Bifida
156
Hirata, O.; Ishikawa, N.; Mizoguchi, Y.; Nakamura, K.; Kobayashi, M.: A Case of Neonatal Coxsackie B2 Meningo-Encephalitis in which Serial Magnetic Resonance Imaging Findings Reveal the Development of Lesions
159
Chiapparini, L.; Savoiardo, M.; D’Arrigo, S.; Reale, C.; Zorzi, G.; Zibordi, F.; Cordelli, D. M.; Franzoni, E.; Garavaglia, B.; Nardocci, N.: The “Eye-of-the-Tiger” Sign may be Absent in the Early Stages of Classic Pantothenate Kinase Associated Neurodegeneration
163
Hirose, M.; Haginoya, K.; Yokoyama, H.; Kikuchi, A.; Hino-Fukuyo, N.; Munakata, M.; Uematsu, M.; Iinuma, K.; Kato, M.; Yamamoto, T.; Tsuchiya, S.: Progressive Atrophy of the Cerebrum in 2 Japanese Sisters with Microcephaly with Simplified Gyri and Enlarged Extraaxial Space
167
Bartolini, L.; Mardari, R.; Toldo, I.; Calderone, M.; Battistella, P. A.; Laverda, A. M.; Sartori, S.: Norovirus Gastroenteritis and Seizures: An Atypical Case with Neuroradiological Abnormalities
170
Poretti, A.; Singhi, S.; Huisman, T.A.G M.; Meoded, A.; Jallo, G.; Ozturk, A.; Boltshauser, E.; Tekes, A.: Tecto-cerebellar Dysraphism with Occipital Encephalocele: Not a Distinct Disorder, but Part of the Joubert Syndrome Spectrum?