DOI: 10.1055/s-00000041

Neuropediatrics

Issue 06 · Volume 51 · December 2020 DOI: 10.1055/s-010-49890

Review Article

389
Tona, Clarissa; Nosadini, Margherita; Pelizza, Maria F.; Pin, Jacopo N.; Baggio, Laura; Boniver, Clementina; Gabrieli, Joseph D.; Causin, Francesco; Toldo, Irene; Sartori, Stefano: Cardiac Myxoma as a Rare Cause of Pediatric Arterial Ischemic Stroke: Case Report and Literature Review

Original Article

397
Heiderich, Sebastian; Dennhardt, Nils; Hartmann, Hans; Kluger, Gerhard Joseph; Sümpelmann, Robert; Herberhold, Thomas: Stability of 0.5% Glucose-Containing Balanced Electrolyte Solutions for Patients on Ketogenic Diets: A Laboratory Study
401
Flotats-Bastardas, Marina; Hahn, Andreas; Schwartz, Oliver; Linsler, Steffan; Meyer, Sascha; Kolodziej, Malgorzata; Koehler, Cornelia: Multicenter Experience with Nusinersen Application via an Intrathecal Port and Catheter System in Spinal Muscular Atrophy
407
Stark, Christina; Duran, Ibrahim; Martakis, Kyriakos; Spiess, Karoline; Semler, Oliver; Schoenau, Eckhard: Effect of Long-Term Repeated Interval Rehabilitation on the Gross Motor Function Measure in Children with Cerebral Palsy

Short Communication

417
Daida, Atsuro; Hamano, Shin-ichiro; Ikemoto, Satoru; Hirata, Yuko; Matsuura, Ryuki; Koichihara, Reiko; Oba, Daiju; Ohashi, Hirofumi: Use of Perampanel and a Ketogenic Diet in Nonketotic Hyperglycinemia: A Case Report
430
Aslanger, Ayca Dilruba; Demiral, Emine; Sonmez-Sahin, Seyma; Guler, Serhat; Goncu, Beyza; Yucesan, Emrah; Iscan, Akın; Saltik, Sema; Yesil, Gozde: Expanding Clinical Phenotype of TRAPPC12-Related Childhood Encephalopathy: Two Cases and Review of Literature
435
Hecher, Laura; Johannsen, Jessika; Bierhals, Tatjana; Buhk, Jan-Hendrik; Hempel, Maja; Denecke, Jonas: The Clinical Picture of a Bilateral Perisylvian Syndrome as the Initial Symptom of Mega-Corpus-Callosum Syndrome due to a MAST1-Gene Mutation
440
Cohen, Rony; Goldberg-Stern, Hadassah; Kivity, Sara; Halevy, Ayelet; Aharoni, Sharon; Kornreich, Liora; Straussberg, Rachel: Evolution of EEG Findings in Pontocerebellar Hypoplasia Type 2A: Normal EEG in the First Few Months followed by Abnormal Tracing over the Years
445
Simsek-Kiper, Pelin Ozlem; Oguz, Sumeyra; Ergen, Fatma Bilge; Utine, Gulen Eda; Alikasifoglu, Mehmet; Haliloglu, Goknur: A Revisited Diagnosis of Collagen VI Related Muscular Dystrophy in a Patient with a Novel COL6A2 Variant and 21q22.3 Deletion

Resident and Fellow Section: Short Communication

425
Giacomini, Thea; Gamucci, Alessandra; Pisciotta, Livia; Nesti, Claudia; Fiorillo, Chiara; Doccini, Stefano; Morana, Giovanni; Nobili, Lino; Santorelli, Filippo M.; Mancardi, Maria Margherita; De Grandis, Elisa: Optic Atrophy and Generalized Chorea in a Patient Harboring an OPA10/RTN4IP1 Pathogenic Variant

Videos and Images in Neuropediatrics

450