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Volume 10 Issue 9, September 2014

Cover image supplied by Carlos Barcia at the Institute of Neuroscience and School of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain. Glial network in the human cortex. Astrocytes with their long processes are immunostained with GFAP antibodies, and microglia with their shorter processes are visualized with IBA1 antibodies. Glial cells form an extensive and uniform network along the brain parenchyma that is crucial for the correct functioning of the CNS. Research on glial cells provides important insights into the pathogenesis of many neurodegenerative diseases and neurological disorders.

Research Highlight

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In Brief

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Research Highlight

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In Brief

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News & Views

  • Many patients with brain tumours possess inadequate mental capacity to provide informed consent, but this situation often goes undetected because clinicians do not routinely conduct formal cognitive assessments. This oversight should be recognized and rectified to enable optimum ethical and medical care of these vulnerable individuals.

    • Mark Bernstein
    News & Views
  • Levodopa is the standard therapy for Parkinson disease, but prolonged use promotes the development of adverse motor effects. A new trial compared the effectiveness of levodopa administration early in the disease with therapies that used alternative dopaminergic agents before levodopa. No clinically relevant differences were found between the treatment strategies.

    • Olivier Rascol
    News & Views
  • Copy number variants (CNVs; deletions or duplications of chromosomal regions) have emerged as an important cause of human disease. In a recent study, epilepsy could be attributed to a pathogenic CNV in 5% of patients, but understanding the implications of a CNV for an individual patient can be challenging.

    • Ingrid E. Scheffer
    • Heather C. Mefford
    News & Views
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Review Article

  • Neuromyelitis optica (NMO) is characterized by inflammatory demyelinating lesions of the spinal cord and optic nerve, and can lead to paralysis and blindness. Currently, several treatment options for NMO exist, but many have been adapted from multiple sclerosis, and no controlled clinical trials specific to NMO have been conducted to date. Here, Marios Papadopoulos and colleagues review the various treatment strategies in NMO, and discuss the drugs that are in development or could be repurposed to treat this condition.

    • Marios C. Papadopoulos
    • Jeffrey L. Bennett
    • Alan S. Verkman
    Review Article
  • Patients with multiple sclerosis (MS) frequently experience depression, which profoundly reduces quality of life, and increases disease mortality. In this Review, Feinstein and colleagues present multiple approaches to the diagnosis and quanitfication of mood disorders, and critically evaluate the various treatment options for MS-related depression.The authors also discuss the extent to which depression can be teased apart from the neurological, immunological and psychosocial sequelae of MS.

    • Anthony Feinstein
    • Sandra Magalhaes
    • Craig Moore
    Review Article
  • In complex regional pain syndromes (CRPS), pain—typically of neuropathic type—in the affected limb is accompanied by a variety of sensory, motor and autonomic signs and symptoms. Treatment for CRPS has been largely adapted from therapies for neuropathic pain states, but a better understanding of CRPS pathologenesis might provide opportunities for mechanism-based treatment. Here, the authors discuss available and emerging mechanism-based treatments in CRPS, including pharmacotherapy targeting central and peripheral sensitization and aberrant inflammatory response; sympathetic ganglion block interventions; and alleviation of symptoms by reversing body perception disturbances.

    • Janne Gierthmühlen
    • Andreas Binder
    • Ralf Baron
    Review Article
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Opinion

  • More than 80% of patients with the demyelinating disorder neuromyelitis optica (NMO) experience pain from this condition, which severely affects their quality of life. NMO-associated pain is largely refractory to contemporary pain therapy, suggesting that the mechanisms underlying pain in NMO differ from those underlying other causes of pain. In this article, Bradl and colleagues explore the mechanisms underlying pain in patients with NMO, and attempt to identify molecular and cellular targets for therapy.

    • Monika Bradl
    • Yoko Kanamori
    • Jürgen Sandkühler
    Opinion
  • Several distinct autoimmune neuropathies can be referred to collectively as Guillain–Barré syndrome (GBS). Wakerley and colleagues argue that confusing terminology hinders diagnosis, and they present a revised classification of 'classic' GBS, Miller Fisher syndrome and related conditions. This new approach to diagnosis might facilitate work-up, thereby helping to identify the correct treatment as quickly as possible.

    • Benjamin R. Wakerley
    • Antonino Uncini
    • Nobuhiro Yuki
    Opinion
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