DOI: 10.1055/s-00000041

Neuropediatrics

Ausgabe 04 · Volume 53 · August 2022 DOI: 10.1055/s-012-54945

Original Article

221
Lund, Josefine; Berring-Uldum, Amalie; Colak, Merve; Debes, Nanette Marinette Monique: Headache in Children and Adolescents: The Association between Screen Time and Headache within a Clinical Headache Population
227
Sharawat, Indar Kumar; Panda, Prateek Kumar: Quality of Life and Its Association with Level of Functioning in Young Children with Cerebral Palsy
235
Manaud, Alice; Geraudie, Amandine; Viguier, Agnès; Mengelle, Catherine; Fortenfant, Françoise; Baudou, Eloïse; Cheuret, Emmanuel: Post-CMV Guillain-Barré Syndrome with Anti-GM2 Antibodies: Two Cases and a Review of the Literature
239
Natsume, Takenori; Inaba, Yuji; Osawa, Yoshihiro; Fukuyama, Tetsuhiro: High Incidence of Hippocampal Abnormalities in Pediatric Patients with Congenital Cytomegalovirus Infection
246
Hayakawa, Katsumi; Tanda, Koichi; Nishimoto, Masakazu; Nishimura, Akira; Kinoshita, Daisuke; Sano, Yuko: The Incidence of Intraventricular Hemorrhage in Low-Birth-Weight Infants: Assessment by Magnetic Resonance Imaging
251
Kasirer, Yair; David, Eliel Ben; Hammerman, Cathy; Shchors, Irina; Nun, Alona Bin: Hypercapnia: An Added Culprit in Gray Matter Injury in Preterm Neonates
257
Zhang, Ruili; Kang, Wenqing; Zhang, Xiaoli; Shi, Lina; Li, Rui; Zhao, Yanmei; Zhang, Jing; Yuan, Xiao; Liu, Shasha; Li, Wenhua; Xu, Falin; Cheng, Xiuyong; Zhu, Changlian: Outcome Analysis of Severe Hyperbilirubinemia in Neonates Undergoing Exchange Transfusion
265
Leitão, Filipa; Grangeia, Ana; Pinto, Joel; Passas, Armanda; Dória, Sofia: Clinical Findings on Chromosome 1 Copy Number Variations
Supplementary Material

Short Communication

274
Delplancq, Geoffroy; Boukebir, Mohamed Abdelatif; Amsallem, Daniel; Thines, Laurent; Rozé, Virginie; Dahlen, Eric; Van Maldergem, Lionel; Kuentz, Paul: The Largest Germline Heterozygous Deletion Encompassing Potocki–Shaffer and WAGR Syndromes Loci to Date: A Case Report
Supplementary Table S1 Supplementary Table S2
279
Sen, Kuntal; Genser, Ilyse; DiFazio, Marc; DiSabella, Marc: Haploinsufficiency of PRRT2 Leading to Familial Hemiplegic Migraine in Chromosome 16p11.2 Deletion Syndrome
283
Alfei, Enrico; Cattaneo, Elisa; Spaccini, Luigina; Iascone, Maria; Veggiotti, Pierangelo; Doneda, Chiara: Progressive Clinical and Neuroradiological Findings in a Child with BCL11B Missense Mutation: Expanding the Phenotypic Spectrum of Related Disorder
287
Chidambaram, Sathya; Manokaran, Ranjith Kumar: Favorable Response to “Memantine” in a Child with GRIN2B Epileptic Encephalopathy
Supplementary Material
291
Cho, Jae Young; Yeom, Jung Sook; Kim, Young-Soo; Choi, Dae-Seob; Park, Ji Sook; Park, Eun Sil; Seo, Ji-Hyun; Lim, Jae-Young; Woo, Hyang-Ok; Park, Chan-Hoo: Neurodevelopmental Outcomes of Neonatal Rotavirus-Associated Leukoencephalopathy
Supplementary Material
295
Kawai, Michiko; Abe, Yuichi; Yumoto, Masato; Kubota, Masaya: Aphasia and a Dual-Stream Language Model in a 4-Year-Old Female with Landau–Kleffner Syndrome
Supplementary Material

Videos and Images in Neuropediatrics

299
Larsh, Travis; Parikh, Sumit: Crossed Cerebellar Diaschisis in EEG Negative Epilepsia Partialis Continua
301
Averdunk, Luisa; Klee, Dirk; Wieczorek, Dagmar; Haack, Tobias B.; Distelmaier, Felix: RANBP2 Mutation Mimicking Viral Encephalitis
303
Nguyen, Khanh; Bazylewicz, Michael P.; Soares, Bruno P.: MOG Antibody Disease Presenting as Multiphasic Disseminated Encephalomyelitis

Letter to the Editor

305
Chang, Min Cheol: Comment: Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome

Reply to Letter to the Editor

306
Meoded, Avner; Kukreja, Marcia; Orman, Gunes; Boltshauser, Eugen; Huisman, Thierry A G M: Reply to "Comment: Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome"

Book Review

308
Boltshauser, Eugen: Children with Vision Impairment