DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 44 · August 2013 DOI: 10.1055/s-003-25345

Editorial

  • 179

    Mitteilungen aus der Gesellschaft für Neuropädiatrie

    • Laudatio

  • 180
    Rating, Dietz:

    Laudatio für Prof. Dr. Dieter Karch anlässlich der Ernennung als Ehrenmitglied der GNP auf der 39. Jahrestagung der Gesellschaft für Neuropädiatrie in Innsbruck

  • 182
    Kurlemann, Gerhard:

    Laudatio für Prof. Dr. Horst Todt anlässlich der Ernennung als Ehrenmitglied der GNP auf der 39. Jahrestagung der Gesellschaft für Neuropädiatrie in Innsbruck

    • Original Article

  • 183
    Visser, Annemarie M.; Jaddoe, Vincent W. V.; Hofman, Albert; Moll, Henriette A.; Arts, Willem Frans M.:

    Validity of Parentally Reported Febrile Seizures: The Generation R Study

  • 187
    Piskin, Ibrahim Etem; Calık, Mustafa; Abuhandan, Mahmut; Kolsal, Ebru; Celik, Sevim Karakas; İscan, Akın:

    PD-1 Gene Polymorphism in Children with Subacute Sclerosing Panencephalitis

  • 191
    Leiba, Hana; Jaggi, Gregor P.; Boltshauser, Eugen; Landau, Klara:

    Prediction of the Clinical Outcome of Cavernous Sinus Lesions in Children

    • Short Communication

  • 199
    Kouga, Takeshi; Iai, Mizue; Yamashita, Sumimasa; Aida, Noriko; Takanashi, Jun-ichi; Osaka, Hitoshi:

    A Child with Three Episodes of Reversible Splenial Lesion

  • 203
    Besch, Dorothea; Makowski, Christine; Steinborn, Marc-Matthias; Bonfig, Walter; Sadowski, Bettina:

    Visual Loss without Headache in Children with Pseudotumor Cerebri and Growth Hormone Treatment

  • 208
    Terek, Demet; Koroglu, Ozge; Yalaz, Mehmet; Gokben, Sarenur; Calli, Cem; Coker, Mahmut; Kultursay, Nilgun:

    Diagnostic Tools of Early Brain Disturbances in an Asymptomatic Neonate with Maple Syrup Urine Disease

  • 213
    Tonduti, Davide; Pichiecchio, Anna; Wolf, Nicole I.; Ariaudo, Giada; van der Knaap, Marjo S.; Bastianello, Stefano; Balottin, Umberto; Orcesi, Simona:

    Novel Hypomyelinating Leukoencephalopathy Affecting Early Myelinating Structures: Clinical Course in Two Brothers

  • 218
    Sakai, Eiko; Yamanaka, Gaku; Kawashima, Hisashi; Morishima, Yasuyuki; Ishida, Yu; Oana, Shingo; Miyajima, Tasuku; Shinohara, Mayu; Saitoh, Makiko; Mizuguchi, Masashi:

    A Case of Recurrent Acute Encephalopathy with Febrile Convulsive Status Epilepticus with Carnitine Palmitoyltransferase II Variation

  • 222
    Cerminara, Caterina; El-Malhany, Nadia; Roberto, Denis; Lo Castro, Adriana; Curatolo, Paolo:

    Seizures Induced by Desloratadine, A Second-Generation Antihistamine: Clinical Observations

  • 225
    Kluger, Gerhard; Koehler, Udo; Neuhann, Teresa M.; Pieper, Tom; Staudt, Martin; von Stülpnagel, Celina:

    Generalized Epilepsy in Two Patients with 5p Duplication

  • 230
    Cole, Theresa S.; McKendrick, Fiona; Cant, Andrew J.; Pearce, Mark S.; Cale, Catherine M.; Goldblatt, David R.; Gennery, Andrew R.; Titman, Penny:

    Cognitive Ability in Children with Chronic Granulomatous Disease: A Comparison of Those Managed Conservatively with Those Who Have Undergone Hematopoietic Stem Cell Transplant

    • Book Review

  • 233

    Children with Neurodevelopmental Disabilities: The Essential Guide to Assessment and Management

  • 234

    Acquired Brain Injury in the Fetus and Newborn

    • Letter to the Editor

  • 235
    Klepper, Joerg:

    Absence of SLC2A1 Mutations Does Not Exclude Glut1 Deficiency Syndrome

    • Erratum

  • 237
    Pini, Giorgio; Bigoni, Stefania; Engerström, Ingegerd Witt; Calabrese, Olga; Felloni, Beatrice; Scusa, Maria Flora; Di Marco, Pietro; Borelli, Paolo; Bonuccelli, Ubaldo; Julu, Peter O. O.; Nielsen, Jytte Bieber; Morin, Bodil; Hansen, Stig; Gobbi, Giuseppe; Visconti, Paola; Pintaudi, Maria; Edvige, Veneselli; Romanelli, Anna; Bianchi, Fabrizio; Casarano, Manuela; Battini, Roberta; Cioni, Giovanni; Ariani, Francesca; Renieri, Alessandra; Benincasa, Alberto; Delamont, Robert S.; Zappella, Michele; ESRRA group:

    Variant of Rett Syndrome and CDKL5 Gene: Clinical and Autonomic Description of 10 Cases