DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 43 · June 2012 DOI: 10.1055/s-002-23334

Review Article

119
Hoche, Franziska; Seidel, Kay; Theis, Marius; Vlaho, Stefan; Schubert, Ralf; Zielen, Stefan; Kieslich, Matthias: Neurodegeneration in Ataxia Telangiectasia: What Is New? What Is Evident?

Original Article

130
Mayr, Johannes A.; Koch, Johannes; Fauth, Christine; Zimmermann, Franz A.; Rauscher, Christian; Zschocke, Johannes; Sperl, Wolfgang: A 1.1 Million Base Pair X-Chromosomal Deletion Covering the PDHA1 and CDKL5 Genes in a Female Patient with West Syndrome and Pyruvate Oxidation Deficiency
135
Kim, Se Hee; Chung, Hye Rim; Kim, Seung Hyo; Kim, Hunmin; Lim, Byung Chan; Chae, Jong Hee; Kim, Ki Joong; Hwang, Yong Seung; Hwang, Hee: Subclinical Hypothyroidism during Valproic Acid Therapy in Children and Adolescents with Epilepsy

Short Communication

140
Khalatbari, Mahmoud Reza; Hamidi, Mehrdokht; Moharamzad, Yashar: Chondromyxoid Fibroma of the Anterior Skull Base Invading the Orbit in a Pediatric Patient: Case Report and Review of the Literature
146
Alicandri-Ciufelli, M.; Soloperto, Davide; Palma, Silvia; Marrara, Antonino; Genovese, Elisabetta: A Clockwork Ear
149
Yimenicioglu, Sevgi; Yakut, Ayten; Erol, Nazmiye; Carman, Kursat; Ekici, Arzu: Chorioretinitis as a First Sign of SSPE
152
Leroy, Sandrine; Gout, Ariel; Husson, Beatrice; de Tournemire, Renault; Tardieu, Marc: Centropontine Myelinolysis Related to Refeeding Syndrome in an Adolescent Suffering from Anorexia Nervosa
155
Alexiou, George A.; Siozos, George; Stefanaki, Kalliopi; Vlachakis, Eustathios; Sfakianos, George; Prodromou, Neofytos; Moschovi, Maria: Medulloblastoma in a Child with Fragile X Syndrome
159
Yalcinkaya, Cengiz; Erturk, Ozdem; Tuysuz, Beyhan; Yesil, Gozde; Verbeke, Jonathan I.M.L.; Keyser, Britta; Stuhrmann, Manfred; Steinemann, Doris; Sistermans, Erik A.; van der Knaap, Marjo S.: A Novel GJC2 Mutation Associated with Hypomyelination and Müllerian Agenesis Syndrome: Coincidence or a New Entity?
162
Kato, Toru; Okumura, Akihisa; Tsuji, Takeshi; Emi, Misugi; Natsume, Jun: Isolated Cystic Lesion of the Callosal Genu after Traumatic Brain Injury
164
Beijer, P.; Lichtenbelt, K.D.; Hofstede, F.C.; Nikkels, P.G.J; Lemmers, P.; de Vries, L.S.: A Known and a Novel Mutation in the Glycine Decarboxylase Gene in a Newborn with Classic Nonketotic Hyperglycinemia
168
Gramer, Gwendolyn; Wolf, Nicole I.; Vater, Daniel; Bast, Thomas; Santer, René; Kamsteeg, Erik-Jan; Wevers, Ron A.; Ebinger, Friedrich: Glucose Transporter-1 (GLUT1) Deficiency Syndrome: Diagnosis and Treatment in Late Childhood

Book Review

172
Willemsen, Michèl A.: Cerebellar Disorders in Children. Clinics in Developmental Medicine No. 191–192