DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 05 · Volume 50 · Oktober 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
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
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
Supplementary Material

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