DOI: 10.1055/s-00000041

Neuropediatrics

Issue 03 · Volume 53 · June 2022 DOI: 10.1055/s-012-54348

Review Article

151
Kingma, Sandra D. K.; Ceulemans, Berten: Recurrent Isolated Sixth Nerve Palsy in Childhood—Review on a Rare Phenomenon

Original Article

159
Nava, Esmeralda; Hartmann, Britta; Boxheimer, Larissa; Capone Mori, Andrea; Nuoffer, Jean-Marc; Sargsyan, Yelena; Thoms, Sven; Rosewich, Hendrik; Boltshauser, Eugen: How to Detect Isolated PEX10-Related Cerebellar Ataxia?
167
Sharma, Yashu; Saini, Arushi Gahlot; Kaur, Rajdeep; Bhatia, Vikas; Didwal, Gunjan; Kumar, Pawan; Uppala, Revathi: Neurodegeneration and Early Infantile Epilepsy Associated with ITPA Variants: A Case Series and Review of Literature
176
Parfyonov, Maksim; Friedlander, Robin; Banno, Brian; Elbe, Dean; Horvath, Gabriella: Psychiatric Manifestations in Patients with Biopterin Defects
182
Baudou, Eloïse; Cances, Claude; Magdelaine, Corinne; Latour, Philippe; Louvier, Ulrike Walther; Juntas-morales, Raul; Cintas, Pascal; Rivier, François: Unexpected Intermediate Nerve Conduction Velocity Findings in Charcot-Marie-Tooth Syndromes Classified as Demyelinated or Axonal in a Pediatric Population
Supplementary Material
188
Ma, Yan; Lu, Xia; Zeng, Gao; Yang, Bin; Jiao, Liqun; Ling, Feng: Vascular Architecture Characters and Changes of Pediatric Moyamoya Disease after Combined Bypass Surgery
Supplementary Material

Short Communication

195
Meoded, Avner; Kukreja, Marcia; Orman, Gunes; Boltshauser, Eugen; Huisman, Thierry A.G.M.: Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome
200
Lee, Hsiu-Fen; Hsu, Chia-Chi; Chi, Ching-Shiang; Tsai, Chi-Ren: Genotype-Phenotype Dissociation in Two Taiwanese Children with Molybdenum Cofactor Deficiency Caused by MOCS2 Mutation
204
Brar, Jagraj S.; Verma, Rahul; Al-Omari, Mohammed; Siu, Victoria M.; Andrade, Andrea V.; Jurkiewicz, Michael T.; Lalgudi Ganesan, Saptharishi: Moyamoya Syndrome in an Infant with Aicardi–Goutières and Williams Syndromes: A Case Report
Supplementary Material
208
Rubino, Alfonso; Bruno, Giorgia; Mazio, Federica; de Leva, Maria Fulvia; Ruggiero, Lucia; Santorelli, Filippo Maria; Varone, Antonio: Spinal Nerve Roots Abnormalities on MRI in a Child with SURF1 Mitochondrial Disease
213
Preusse, Matthias; Paraschaki, Georgia; Lutz, Soeren: A Case of ECHS1 Deficiency with Severe Encephalopathy and Status Epilepticus after a Propofol Sedation: Case Report

Videos and Images in Neuropediatrics

217
Depierreux, Frédérique; Alkan, Serpil: Atypical Hemifacial Spasm and Myoclonus Related to AIFM1 Variant
218
Means, Margaret J.; Santos, Francis J. R.; Sotardi, Susan T.; Beslow, Lauren A.: Menkes Disease: Clinical Presentation and Imaging Characteristics