Reply:

References

1. 1.↵
   2. Sone J,
   3. Nakamura T,
   4. Koike H, et al

   . Reply: neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma. Brain 2017;140:e52 doi:10.1093/brain/awx158 e52 pmid:28899012

   CrossRefPubMed
2. 2.↵
   2. Sone J,
   3. Kitagawa N,
   4. Sugawara E, et al

   . Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy. J Neurol Neurosurg Psychiatry 2014;85:354–56 doi:10.1136/jnnp-2013-306084 pmid:24039026

   FREE Full Text
3. 3.↵
   2. Hirose B,
   3. Hisahara S,
   4. Uesugi H, et al

   . Sporadic adult-onset neuronal intranuclear inclusion disease with abnormal electroretinogram, nerve conduction studies and somatosensory evoked potential [in Japanese]. Rinsho Shinkeigaku 2018;58:407–10 doi:10.5692/clinicalneurol.cn-001154 pmid:29863097

   CrossRefPubMed
4. 4.↵
   2. Sone J,
   3. Mori K,
   4. Inagaki T, et al

   . Clinicopathological features of adult-onset neuronal intranuclear inclusion disease. Brain 2016;139:3170–86 doi:10.1093/brain/aww249 pmid:27797808

   CrossRefPubMed
5. 5.↵
   2. Takahashi-Fujigasaki J,
   3. Nakano Y,
   4. Uchino A, et al

   . Adult-onset neuronal intranuclear hyaline inclusion disease is not rare in older adults. Geniatr Gernotol Int 2016;16(Suppl 1):51–56 doi:10.1111/ggi.12725 pmid:27018283

   CrossRefPubMed
6. 6.↵
   2. Ishii K,
   3. Hosaka Ai,
   4. Adachi K, et al

   . A Japanese case of fragile-X-associated tremor/ataxia syndrome (FXTAS). Intern Med 2010;49:1205–08 doi:10.2169/internalmedicine.49.3258 pmid:20558944

   CrossRefPubMed