Genetic and Imaging Characteristics of a Family With Neuronal Intranuclear Inclusion Disease

참고문헌 (9)

1. Sone J, "Clinicopathological features of adult-onset neuronal intranuclear inclusion disease", Brain, 139(Pt 12), pp.3170~3186 (2016)
2. Deng J, "Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease", J Med Genet (2021)
3. Ogasawara M, "CGG expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy with neurological manifestations", Acta Neuropathol Commun, 8, pp.204~ (2020)
4. Okamura S, "A case of neuronal intranuclear inclusion disease with recurrent vomiting and without apparent DWI abnormality for the first seven years", Heliyon, 6, pp.e04675~ (2020)
5. Sugiyama A, "MR imaging features of the cerebellum in adult-onset neuronal intranuclear inclusion disease : 8 cases", AJNR Am J Neuroradiol, 38, pp.2100~2104 (2017)
6. 전민영, "Adult-Onset Neuronal Intranuclear Inclusion Disease: First Korean Case Confirmed by Skin Biopsy", Journal of Clinical Neurology, 16(4), pp.720~722 (2020), 대한신경과학회[DOI]
7. 양태원, "반복되는 두통과 혼동 그리고 점차 진행하는 인지기능장애로 발현한 신경세포핵내봉입체병", 대한신경과학회지, 38(4), pp.342~345 (2020), 대한신경과학회
8. Sone J, "Neuronal intranuclear hyaline inclusion disease showing motorsensory and autonomic neuropathy", Neurology, 65, pp.1538~1543 (2005)
9. Liu X, "A case of recurrent vomiting : extending the spectrum of neuronal intranuclear inclusion disease", Neurol Sci, 40, pp.2661~2664 (2019)