DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 06 · Volume 48 · Dezember 2017 DOI: 10.1055/s-007-35262

Review Article

  • 403
    Anestis, Dimitrios M.; Tsitsopoulos, Parmenion P.; Ble, Christina A.; Tsitouras, Vassilios; Tsonidis, Christos A.:

    Congenital Glioblastoma Multiforme: An Unusual and Challenging Tumor

  • 413
    Magalhães, Luiza Vieira da Silva; Winckler, Maria Isabel Bragatti; Bragatti, José Augusto; Procianoy, Renato; Silveira, Rita de Cássia Santos:

    The Role of Amplitude Integrated Electroencephalogram in Very Low-Birth-Weight Preterm Infants: A Literature Review

    • Original Article

  • 420
    Vill, Katharina; Ille, Lena; Blaschek, Astrid; Rawer, Rainer; Landgraf, Mirjam N.; Gerstl, Lucia; Schroeder, Sebastian A.; Müller-Felber, Wolfgang:

    Jumping Mechanography as a Complementary Testing Tool for Motor Function in Children with Hereditary Motor and Sensory Neuropathy

    Supplementary Figure (PDF)
  • 426
    Chen, Na; Wang, Jingmin; Jiang, Yuwu; Wu, Ye; Hao, Hongjun; Ji, Taoyun:

    Different Mutations of Gap Junction Connexin 47 Lead to Discrepant Activation of Unfolded Protein Response Pathway in Pelizaeus–Merzbacher-Like Disease

  • 432
    Wilbrand, Jan-Falco; Kaps, Kerstin; Tabak, Darko; Bierther, Uta; Wilbrand, Martina; Neubauer, Bernd Axel; Pons-Kuehnemann, Joern; Howaldt, Hans-Peter; Hahn, Andreas:

    Normal Head Shape Parameters in the First 2 Years of Life and Effect of Helmet Therapy

  • 442
    Navarro-Cobos, María José; González-del Angel, Ariadna; Estandia-Ortega, Bernardette; Ruiz-Herrera, Adriana; Becerra, Arturo; Vargas-Ramírez, Guadalupe; Bermúdez-López, Cesárea; Alcántara-Ortigoza, Miguel Angel:

    Molecular Analysis Confirms that FKRP-Related Disorders are Underdiagnosed in Mexican Patients with Neuromuscular Diseases

    Video vorhanden
    Supplementary Material (PDF)

    • Short Communication

  • 451
    Grzybowski, Michelle; Schänzer, Anne; Pepler, Alexander; Heller, Corina; Neubauer, Bernd A.; Hahn, Andreas:

    Novel STAC3 Mutations in the First Non-Amerindian Patient with Native American Myopathy

    Supplementary Table (PDF)
  • 456
    Kropach, Nesia; Shkalim-Zemer, Vered; Orenstein, Naama; Scheuerman, Oded; Straussberg, Rachel:

    Novel RRM2B Mutation and Severe Mitochondrial DNA Depletion: Report of 2 Cases and Review of the Literature

  • 463
    Doneda, Chiara; Pinelli, Lorenzo; Scaramuzzi, Matteo; Galli, Jessica; Fazzi, Elisa; Parazzini, Cecilia; Righini, Andrea; Nucci, Paolo:

    Morning Glory Disc Anomaly Associated with Ipsilateral Optic Nerve and Chiasm Thickening: Three Cases and Review of the Literature

  • 467
    Komulainen-Ebrahim, Jonna; Saastamoinen, Eemeli; Rahikkala, Elisa; Helander, Heli; Hinttala, Reetta; Risteli, Leila; Rantala, Heikki; Uusimaa, Johanna:

    Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis

  • 473
    Tard, Céline; Tiffreau, Vincent; Jaillette, Emmanuelle; Jouen, Fabienne; Nelson, Isabelle; Bonne, Gisèle; Yaou, Rabah Ben; Romero, Norma; Vallée, Louis; Vermersch, Patrick; Nguyen, Sylvie; Maurage, Claude-Alain; Cuisset, Jean-Marie:

    Anti-HMGCR Antibody–Related Necrotizing Autoimmune Myopathy Mimicking Muscular Dystrophy

  • 477
    Ardicli, Didem; Taskiran, Ekim Z.; Kosukcu, Can; Temucin, Cagri; Oguz, Kader K.; Haliloglu, Goknur; Alikasifoglu, Mehmet; Topaloglu, Haluk:

    Neonatal-Onset Recurrent Guillain–Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency

    Supplementary Table (PDF)

    • Videos and Images in Neuropediatrics

  • 482
    Rommel, Frank R.; Miske, Ramona; Stöcker, Winfried; Arneth, Borros; Neubauer, Bernd A.; Hahn, Andreas:

    Chorea Minor Associated with Anti-Neurochondrin Autoantibodies

    Video vorhanden

    • Book Review

  • 484
    Bölsterli Heinzle, Bigna Katrin:

    The Epilepsy-Aphasia Spectrum: From Landau–Kleffner Syndrome to Rolandic Epilepsy