A case of neuronal intranuclear inclusion disease with serial MRI changes observed from before onset of forgetfulness
Author:
Affiliation:
1. Department of Neurology, Saiseikai Otaru Hospital
2. Department of Neurology, National Hospital Organization Suzuka National Hospital
3. Department of Neurology, Sapporo Medical University School of Medicine
Publisher
Societas Neurologica Japonica
Subject
Neurology (clinical)
Link
https://www.jstage.jst.go.jp/article/clinicalneurol/61/11/61_cn-001609/_pdf
Reference22 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) Sone J, Tanaka F, Koike H, et al. Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease. Neurology 2011;76:1372-1376.
3. 3) Sone J, Mitsuhashi S, Fujita A, et al. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease. Nat Genet 2019;51:1215-1221.
4. 4) Sone J, Mori K, Inagaki T, et al. Clinicopathological features of adult-onset neuronal intranuclear inclusion disease. Brain 2016;139:3170-3186.
5. 5) Zannolli R, Gilman S, Rossi S, et al. Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration. Arch Neurol 2002;59:1319-1326.
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