DOI: 10.1055/s-00000041

Neuropediatrics

Issue 04 · Volume 48 · August 2017 DOI: 10.1055/s-007-34473 Neuromuscular Disorders in Children and Adolescents Guest Editor: Rudolf Korinthenberg, MD.

Editorial

  • 209
    Korinthenberg, Rudolf:

    Neuromuscular Disorders in Children and Adolescents

    • Review Article

  • 211
    Leary, Rebecca; Oyewole, Anne O.; Bushby, Katharine; Aartsma-Rus, Annemieke:

    Translational Research in Europe for the Assessment and Treatment for Neuromuscular Disorders (TREAT-NMD)

  • 221
    Müller-Felber, Wolfgang; Vill, Katharina:

    Clinical Neurophysiology in Neuromuscular Disorders: Old Fashioned or Still Relevant?

  • 226
    Stenzel, Werner; Schoser, Benedikt:

    Inherited and Acquired Muscle Weakness: A Moving Target for Diagnostic Muscle Biopsy

  • 233
    Warman Chardon, Jodi; Straub, Volker:

    The Role of Muscle Imaging in the Diagnosis and Assessment of Children with Genetic Muscle Disease

  • 242
    Kress, Wolfram; Rost, Simone; Kolokotronis, Konstantin; Meng, Gerhard; Pluta, Natalie; Müller-Reible, Clemens:

    The Genetic Approach: Next-Generation Sequencing-Based Diagnosis of Congenital and Infantile Myopathies/Muscle Dystrophies

  • 247
    Schorling, David C.; Kirschner, Janbernd; Bönnemann, Carsten G.:

    Congenital Muscular Dystrophies and Myopathies: An Overview and Update

  • 262
    Domingos, Joana; Sarkozy, Anna; Scoto, Mariacristina; Muntoni, Francesco:

    Dystrophinopathies and Limb-Girdle Muscular Dystrophies

  • 273
    Pechmann, Astrid; Kirschner, Janbernd:

    Diagnosis and New Treatment Avenues in Spinal Muscular Atrophy

  • 282
    Rudnik-Schöneborn, Sabine; Auer-Grumbach, Michaela; Senderek, Jan:

    Hereditary Neuropathies: Update 2017

  • 294
    McMacken, Grace; Abicht, Angela; Evangelista, Teresinha; Spendiff, Sally; Lochmüller, Hanns:

    The Increasing Genetic and Phenotypical Diversity of Congenital Myasthenic Syndromes

  • 309
    Wortmann, Saskia B.; Mayr, Johannes A.; Nuoffer, Jean Marc; Prokisch, Holger; Sperl, Wolfgang:

    A Guideline for the Diagnosis of Pediatric Mitochondrial Disease: The Value of Muscle and Skin Biopsies in the Genetics Era

    Supplementary Data (PDF)

    • Original Article

  • 315
    Della Marina, Adela; Kölbel, Heike; Müllers, Maximilian; Kaiser, Olaf; Ismail, Mahmoud; Swierzy, Marc; Rueckert, Jens-Carsten; Schara, Ulrike:

    Outcome after Robotic-Assisted Thymectomy in Children and Adolescents with Acetylcholine Receptor Antibody-Positive Juvenile Myasthenia Gravis