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
  • 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