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
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
Supplementary Material

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
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

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

Book Review

484
Bölsterli Heinzle, Bigna Katrin: The Epilepsy-Aphasia Spectrum: From Landau–Kleffner Syndrome to Rolandic Epilepsy