DOI: 10.1055/s-00000041

Neuropediatrics

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

Original Article

  • 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

    Open Access
  • 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

    • 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 (PDF) Supplementary Table S2 (PDF)
  • 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 (PDF)
  • 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 (PDF)
  • 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 (PDF)

    • 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

  • Leitão, Filipa; Grangeia, Ana; Pinto, Joel; Passas, Armanda; Dória, Sofia:

    Clinical Findings on Chromosome 1 Copy Number Variations

    Supplementary Material (PDF)
  • 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