DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 56 · August 2025 DOI: 10.1055/s-015-61954

Editorial

  • 213
  • Review Article

  • 215
    Gellrich, Janine; Lohrer, Elisabeth C.; Hummel, Thomas; Schriever, Valentin A.:

    Olfactory Dysfunction in Children and Adolescents—A Diagnostic Pathway

  • 221
    Lieftüchter, Victoria; Vollmuth, Yannik; Tacke, Moritz; Hoffmann, Florian; Paolini, Marco; Finck, Tom; Liesche-Starnecker, Friederike; von Both, Ulrich; Pörtner, Kirsten; Tappe, Dennis; Grosse, Leonie:

    Bornavirus (BoDV-1) Encephalitis in Children: Update on Diagnosis and Treatment

  • Original Article

  • 226
    Fellmeth, Ruth Helena; Kousoulos, Lampros; Korenke, George Christoph; Christen, Hans-Jürgen; Monazahian, Masyar; Dargvainiene, Justine; Wandinger, Klaus-Peter; Leypoldt, Frank; Rostásy, Kevin:

    MOG-Encephalitis is the Most Prevalent Autoimmune Encephalitis in Children: MERIN Study Data on Encephalitis

  • 234
  • 241
    Doğan, Gizem; Sarıkaya Uzan, Gamze; Güzin, Yiğithan; Baydan, Figen; Eliacık, Kayı; Güven, Barıs; Bakiler, Ali Rahmi:

    The Effect of Genotype Differences on Cardiac Involvement in Cases Diagnosed with Duchenne Muscular Dystrophy

  • 249
    Quade, Annegret; Lischka, Annette; Albani, Simone; Rossetti, Giulia; Hageb, Zahra-Nada; Rolke, Roman; Kurth, Ingo; Katona, Istvan Kristof; Eggermann, Katja; Namer, Barbara; Lampert, Angelika; Dohrn, Maike F.; Schacht, Gabriel M.; Weis, Joachim; Häusler, Martin:

    Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic Pain

  • Short Communication

  • 259
    D'Eleuterio, Annalisa; Rufini, Paolo; L'Erario, Manuela; Simonini, Gabriele; Montagnani, Carlotta; Ermini, Stefano; Ricci, Silvia; Bartolini, Luca; Ricci, Zaccaria:

    Management of Critically Ill Children with Acute Necrotizing Encephalitis during an H1N1 Outbreak in a Tertiary Pediatric Hospital: A Series of Three Cases and Literature Review

  • 265
    Mouraux, Charlotte; Alkan, Serpil; Caberg, Jean-Hubert; Depierreux, Frédérique:

    Association between CACNA1A and ATP1A2 Variants are Responsible for Severe Neurodevelopmental Disorder

  • 269
    Avsenik, Jernej; Benedik, Mirjana P.; Rogač, Mihael; Biswas, Asthik; Sudhakar, Sniya; D'Arco, Felice; Löbel, Ulrike; Mankad, Kshitij:

    Divergent Presentation of GRIN2B Neurodevelopmental Disorder in Monozygotic Twins: Case Report with Unique Imaging Phenotypes

  • 274
    Basch, Rebecca E.; Tierney, McKenna; Worden, Lila; Sanders, Sara; Ng, Elizabeth A.:

    EBV and Concomitant Acute Motor and Sensory Axonal Neuropathy in a Healthy 15-Year-Old Female

  • Videos and Images in Neuropediatrics

  • 278
    Kronast, Lorenz; Schweikart, Sarah; Jakob, Marcus; Studt, Friederike; Kluger, Gerhard; Hartlieb, Till:

    Combined Gelastic and Dacrystic Seizures in a Child with Hypothalamic Hamartoma