DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

Ausgabe 05 · Volume 21 · Oktober 2023 DOI: 10.1055/s-013-58371 Pediatric Neuroradiology

Review Article

  • 329
    Rana, Abhilasha; Krishnan, Venkatram; Jamwal, Rupie:

    Spinal Dysraphism Spectrum: A Novel Protocol-based Approach for Accurate Diagnosis on Imaging

    • Original Article

  • 341
    Gowda, Vykuntaraju K.; Channabasappa, Basavakumar; Shivappa, Sanjay K.; Veerappa, Basavaraja G.; Lakshmikantha, Keshavamurthy Mysore:

    The Clinical, Laboratory, Etiological Profile and Outcome of Acute Necrotizing Encephalitis of Childhood (ANEC) in Tertiary Care Centre from Southern India

  • 347
    Cebeci, Hakan; Rykken, Jeffrey; Ott, Frederick; Folkertsma, Mark; Koksel, Yasemin; Gencturk, Mehmet:

    Microstructural Changes in Normal-Appearing White Matter in Pediatric X-Linked Adrenoleukodystrophy: A Diffusion Tensor Imaging Study

  • 352
    Hassanein, Sahar M.A.; Elagouza, Iman; Sakr, Hossam; Mohammed, Maha Z.; Rihan, Ahmed; Deifalla, Shaymaa:

    Diaphragmatic and Rectus Femoris Muscles Ultrasonography in Relation to Motor and Respiratory Functions in Ambulatory Boys with Duchenne Muscular Dystrophy

    • Case Report

  • 360
    Bastos, Paulo André Dias; Barbosa, Raquel:

    A Newly Identified Int22h1/Int22h2‐Mediated Xq28 Duplication Syndrome Case Misdiagnosed as Cerebral Palsy

    Video vorhanden
  • 365
    Shabo, Leah; Ishaque, Mariam; Sarathy, Danyas; Kumar, Jeyan; Xixis, Kathryn; Park, Min:

    Pediatric Tacrolimus-Induced Reversible Cerebral Vasoconstriction Syndrome after Heart Transplantation

  • 371
    Samur, Bahadir M.; Ercan-Sencicek, Gulhan A.; Gumus, Hakan; Gumus, Gulsum; Baykan, Ali; Caglayan, Ahmet Okay; Per, Huseyin:

    Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1

  • 377
    Das, Suman; Ray, Biman K.; Chakraborty, Uddalak; Kabiraj, Sujoy:

    A Novel Variant of the Short-Chain Enoyl-CoA Hydratase-1 Gene Presenting with a Mild Phenotype: The Second Case Report from India

  • 384
    Freitas, Leonardo F.; Ribeiro, Lays S.; Duarte, Márcio L.; Silva, Mayara O. da; Ferreira, Paula M.:

    Coffin–Siris Syndrome in a Patient with Hirschsprung's Disease—Expanding the Phenotype by Mutation ARID1B: A Case Report and Literature Review

  • 388
    Singh, Kushagra; Lohiya, Sham; Ganvir, Shubhangi; Damke, Sachin:

    A Case of Acute Necrotizing Encephalitis Following Coronavirus Disease 2019 Infection—A Rare Presentation

  • 391
    Jain, Mukesh Kumar; Behera, Chinmaya Kumar; Panda, Sangram; Patnaik, Sibabratta; Sahoo, Bandya; Mishra, Reshmi; Behera, Jyoti Ranjan:

    A Rare Case of Encephalopathy in Children—Known but Unknown

  • 395
    Yadav, Kusumlata; Mishra, Arpita; Narayan, Raghvendra; Singh, Ashok; Agrawal, Ritesh; Mishra, Om Prakash:

    Homocystinuria Presenting as Ectopia Lentis and Thrombotic Manifestations in Two Siblings: A Case Series

  • 399
    Nagabushana, Divya; Samaga, Vishal Vishnuram; Shenoy, Sangeetha; Girishan, Shabari; V. Reddy, Hamsa; AR, Somashekhar:

    Coronavirus Disease 2019-Associated Cerebral Mucormycosis in an Immunocompetent Child

  • 404
    Oyuela-Mancera, Martha E.; Maturana, Jennifer R.; Rodriguez, Laura C.; Perez-Acosta, Juan J.; Rodado-Mieles, César E.; Bastidas, Nicolás:

    Thalamic Gangliocytoma in a Pediatric Patient—An Incidental Diagnosis

    • Letter to the Editor

  • 408
    Huddar, Akshata; Govindaraj, Periyasamy; Chiplunkar, Shwetha; Nagappa, Madhu; Taly, Arun B.; Sankaran, Bindu Parayil:

    Paroxysmal Dystonia in a Child with Enoyl-CoA Hydratase Short-Chain 1 (ECHS1) Mutations

    • Erratum

  • e1
    Samur, Bahadir M.; Ercan-Sencicek, Gulhan A.; Gumus, Hakan; Gumus, Gulsum; Baykan, Ali; Caglayan, Ahmet Okay; Per, Huseyin:

    Erratum: Childhood-Onset Neurodegeneration with Cerebellar Atrophy Syndrome: Severe Neuronal Degeneration and Cardiomyopathy with Loss of Tubulin Deglutamylase Cytosolic Carboxypeptidase 1