DOI: 10.1055/s-00000041

Neuropediatrics

Issue 05 · Volume 50 · October 2019 DOI: 10.1055/s-009-44132

Review Article

  • 273
    Santoro, Jonathan D.; Chitnis, Tanuja:

    Diagnostic Considerations in Acute Disseminated Encephalomyelitis and the Interface with MOG Antibody

  • 280
    Ramantani, Georgia; Schmitt, Bernhard; Plecko, Barbara; Pressler, Ronit M.; Wohlrab, Gabriele; Klebermass-Schrehof, Katrin; Hagmann, Cornelia; Pisani, Francesco; Boylan, Geraldine B.:

    Neonatal Seizures—Are We there Yet?

    • Original Article

  • 294
    Ebrahimi-Fakhari, Daniel; Hussong, Justine; Flotats-Bastardas, Marina; Ebrahimi-Fakhari, Darius; Zemlin, Michael; von Gontard, Alexander; Meyer, Sascha:

    Tuberous Sclerosis Complex Associated Neuropsychiatric Disorders and Parental Stress: Findings from a National, Prospective TSC Surveillance Study

    • Short Communication

  • 300
    Vaassen, Pia; Dürr, Nikola; Röhrig, Andreas; Willing, Rainer; Rosenbaum, Thorsten:

    Trametinib Induces Neurofibroma Shrinkage and Enables Surgery

  • 304
    Hardy, Duriel I.; Licht, Daniel J.; Vossough, Arastoo; Kirschen, Matthew P.:

    X-linked Charcot–Marie–Tooth Disease Presenting with Stuttering Stroke-like Symptoms

  • 308
    Zimmern, Vincent; Riant, Florence; Roze, Emmanuel; Ranza, Emmanuelle; Lehmann-Horn, Frank; de Bellescize, Julitta; Ville, Dorothée; Lesca, Gaetan; Korff, Christian M.:

    Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 Mutation

    Video available
  • 313
    Gowda, Vykuntaraju K.; Srinivasan, Varunvenkat M.; Jehta, Kapil; Bhat, Maya D.:

    Bilateral Striatal Necrosis with Polyneuropathy with a Novel SLC25A19 (Mitochondrial Thiamine Pyrophosphate Carrier OMIMI*606521) Mutation: Treatable Thiamine Metabolic Disorder—A Report of Two Indian Cases

  • 318
    Madaan, Priyanka; Jauhari, Prashant; Chakrabarty, Biswaroop; Kumar, Atin; Gulati, Sheffali:

    Saposin B–Deficient Metachromatic Leukodystrophy Mimicking Acute Flaccid Paralysis

  • 322
    Lee, Yun Jeong; Oh, Jeeyoung; Hwang, Su-Kyeung; Lee, Eun Joo; Yang, Dong Heon; Kim, Yong-Jin; Kwon, Soonhak; Hyun, Myung Chul:

    Extremely Early Onset Transthyretin Familial Amyloid Polyneuropathy with a Leu55Pro Mutation: A Pediatric Case Report and Literature Review

    Supplementary Material (PDF)
  • 327
    Giacomini, Thea; Vari, Maria Stella; Janis, Sara; Prato, Giulia; Pisciotta, Livia; Rocchi, Alessia; Michelucci, Angela; Di Rocco, Maja; Gandullia, Paolo; Mattioli, Girolamo; Sacco, Oliviero; Morana, Giovanni; Mancardi, Maria Margherita:

    Epileptic Encephalopathy, Myoclonus–Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene

    Video available
    Supplementary Material (PDF)

    • Images in Neuropediatrics

  • 332
    Gelebart, Clémentine; Sacaze, Elise; Peudenier, Sylviane; Legeas, Olivier; Ropars, Juliette:

    A Hemimotor Deficit in an 18-Month-Old Boy Revealing Acute Myelitis

  • 334
    Esposito, Silvia; Moscatelli, Marco; Schiariti, Marco Paolo; Viganò, Ilaria; Pantaleoni, Chiara; Marucci, Gianluca:

    Pott's Disease: An Emerging Source of Potentially Inappropriate Treatment

    • Letter to Editor

  • 336
    Gorukmez, Orhan; Gorukmez, Ozlem; Havalı, Cengiz:

    Novel MECR Mutation in Childhood-Onset Dystonia, Optic Atrophy, and Basal Ganglia Signal Abnormalities

    • Book Review

  • 338
    Kuenzle, Christoph:

    Children and Youth with Complex Cerebral Palsy: Care and Management