Neuronal intranuclear inclusion disease (NIID)
Author:
Affiliation:
1. Department of Neurology, National Hospital Organization Suzuka National Hospital
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/60/10/60_cn-001417/_pdf
Reference44 articles.
1. 1) Lindenberg R, Rubinstein LJ, Herman MM, et al. A light and electron microscopy study of an unusual widespread nuclear inclusion body disease. A possible residuum of an old herpesvirus infection. Acta Neuropathol (Berl) 1968;10:54-73.
2. 2) Oyer CE, Cortez S, O’Shea P, et al. Cardiomyopathy and myocyte intranuclear inclusions in neuronal intranuclear inclusion disease: a case report. Hum Pathol 1991;22:722-724.
3. 3) Kimber TE, Blumbergs PC, Rice JP, et al. Familial neuronal intranuclear inclusion disease with ubiquitin positive inclusions. J Neurol Sci 1998;160:33-40.
4. 4) Sung JH. Light, fluorescence, and electron microscopic features of neuronal intranuclear hyaline inclusions associated with multisystem atrophy. Acta Neuropathol 1980;50:115-120.
5. 5) Funata N, Maeda Y, Koike M, et al. Neuronal intranuclear hyaline inclusion disease: report of a case and review of the literature. Clin Neuropathol 1990;9:89-96.
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1. A Case of Neuronal Intranuclear Inclusion Disease Diagnosed Definitively from Skin Tissue;The Nishinihon Journal of Dermatology;2023-12-01
2. Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective review;Frontiers in Neurology;2022-12-15
3. Recent topics of neuronal intranuclear inclusion disease ( NIID );Neurology and Clinical Neuroscience;2022-11-14
4. Brain Cell Type-Specific Nuclear Proteomics Is Imperative to Resolve Neurodegenerative Disease Mechanisms;Frontiers in Neuroscience;2022-06-16
5. Neuronal intranuclear inclusion disease in a patient who exhibited abnormal behavior;Rinsho Shinkeigaku;2022
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