Motor-neuron-disease-like phenotype associated with IgLON5 disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Neurology
Link
https://link.springer.com/content/pdf/10.1007/s00415-022-11262-0.pdf
Reference11 articles.
1. Landa J et al (2020) Effects of IgLON5 antibodies on neuronal cytoskeleton: a link between autoimmunity and neurodegeneration. Ann Neurol 88(5):1023–1027
2. Sabater L et al (2014) A novel non-rapid-eye movement and rapid-eye-movement parasomnia with sleep breathing disorder associated with antibodies to IgLON5: a case series, characterisation of the antigen, and post-mortem study. Lancet Neurol 13(6):575–586
3. Gaig C, Compta Y (2019) Neurological profiles beyond the sleep disorder in patients with anti-IgLON5 disease. Curr Opin Neurol 32(3):493–499
4. Wenninger S (2017) Expanding the clinical spectrum of IgLON5-syndrome. J Neuromuscul Dis 4(4):337–339
5. Honorat JA et al (2017) IgLON5 antibody: neurological accompaniments and outcomes in 20 patients. Neurol-Neuroimmunol Neuroinflamm 4(5):e385
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1. IgLON5 deficiency produces behavioral alterations in a knockout mouse model;Frontiers in Immunology;2024-02-02
2. Papillitis associated with IgLON5 autoimmunity: A novel clinical phenotype;Journal of Neuroimmunology;2024-02
3. Progressive Orthopnea and Bendopnea Due to Diaphragmatic Paralysis Associated With IgLON5 Autoimmunity;Mayo Clinic Proceedings;2023-07
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