Sporadic adult-onset neuronal intranuclear inclusion disease with abnormal electroretinogram, nerve conduction studies and somatosensory evoked potential-Reference-Cited by-同舟云学术

Sporadic adult-onset neuronal intranuclear inclusion disease with abnormal electroretinogram, nerve conduction studies and somatosensory evoked potential

Published:2018 Issue:6 Volume:58 Page:407-410
ISSN:0009-918X
Container-title:Rinsho Shinkeigaku
language:en
Short-container-title:Rinsho Shinkeigaku

Author:

Hirose Bungo¹,Hisahara Shin¹,Uesugi Haruo²,Sone Jun³,Sobue Gen³,Shimohama Shun¹

Affiliation:

1. Department of Neurology, Sapporo Medical University School of Medicine

2. Department of Neurology, Sapporo Yamanoue Hospital

3. Department of Neurology, Nagoya University Graduate School of Medicine

Publisher

Societas Neurologica Japonica

Subject

Clinical Neurology

Link

https://www.jstage.jst.go.jp/article/clinicalneurol/58/6/58_cn-001154/_pdf

Reference7 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 1968;10:54-73.

2. 2) Sone J, Mori K, Inagaki T, et al. Clinicopathological features of adult-onset neuronal intranuclear inclusion disease. Brain 2016;139:3170-3186.

3. 3) 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.

4. 4) Haltia M, Tarkkanen A, Somer H, et al. Neuronal intranuclear inclusion disease. Clinical ophthalmological features and ophthalmic pathology. Acta Ophthalmol 1986;64:637-643.

5. 5) Arrindell EL, Trobe JD, Sieving PA, et al. Pupillary and electroretinographic abnormalities in a family with neuronal intranuclear hyaline inclusion disease. Arch Ophthalmol 1991;109:373-378.

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