Cargando…

Adult-Onset Neuronal Intranuclear Inclusion Disease: First Korean Case Confirmed by Skin Biopsy

Detalles Bibliográficos
Autores principales:	Chun, Min Young, Park, Hee Kyung, Kim, Geon Ha, Lee, Seung-Ah, Kim, Soo-Hyun, Sung, Sun Hee, Park, Yae Won, Jeong, Jee Hyang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Neurological Association 2020
Materias:	Letter to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7541984/ https://www.ncbi.nlm.nih.gov/pubmed/33029987 http://dx.doi.org/10.3988/jcn.2020.16.4.720

Ejemplares similares

Urine cytological study in patients with clinicopathologically confirmed neuronal intranuclear inclusion disease
por: Zhou, Yiyi, et al.
Publicado: (2022)

The Value of NOTCH2NLC Gene Detection and Skin Biopsy in the Diagnosis of Neuronal Intranuclear Inclusion Disease
por: Pang, Jie, et al.
Publicado: (2021)

Clinicopathological features of adult-onset neuronal intranuclear inclusion disease
por: Sone, Jun, et al.
Publicado: (2016)

FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report
por: Toko, Megumi, et al.
Publicado: (2021)

Case Report: Neuronal Intranuclear Inclusion Disease With Oromandibular Dystonia Onset
por: Deng, Wei-Ping, et al.
Publicado: (2021)

Correction to: FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report
por: Toko, Megumi, et al.
Publicado: (2021)

Adult‐onset neuronal intranuclear inclusion disease presenting with typical MRI changes
por: Han, Xinsheng, et al.
Publicado: (2019)

Intranuclear inclusions in muscle biopsy can differentiate oculopharyngodistal myopathy and oculopharyngeal muscular dystrophy
por: Ogasawara, Masashi, et al.
Publicado: (2022)

Neuronal intranuclear inclusion disease is genetically heterogeneous
por: Chen, Zhongbo, et al.
Publicado: (2020)

Case report: Adult-onset neuronal intranuclear inclusion disease with an amyotrophic lateral sclerosis phenotype
por: Fujita, Masako, et al.
Publicado: (2022)

Clinical-neuroimaging-pathological relationship analysis of adult onset Neuronal Intranuclear Inclusion Disease (NIID)
por: Mao, Chenhui, et al.
Publicado: (2022)

Adult-onset neuronal intranuclear inclusion disease, with both stroke-like onset and encephalitic attacks: a case report
por: Huang, Ying, et al.
Publicado: (2021)

Essential tremor with ubiquitinated intranuclear inclusions and cerebellar degeneration
por: Louis, Elan D., et al.
Publicado: (2012)

Neuronal Intranuclear Inclusion Disease Presenting with Resting Tremor
por: Kitagawa, Naoyuki, et al.
Publicado: (2014)

Intranuclear inclusions in a fragile X mosaic male
por: Pretto, Dalyir I, et al.
Publicado: (2013)

Characterization of two types of intranuclear hepatocellular inclusions in NAFLD
por: Schwertheim, Suzan, et al.
Publicado: (2020)

Myoclonic Epilepsy with Ragged-red Fibers with Intranuclear Inclusions
por: Kawazoe, Tomoya, et al.
Publicado: (2021)

Clinical and mechanism advances of neuronal intranuclear inclusion disease
por: Liu, Yueqi, et al.
Publicado: (2022)

Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease
por: Tai, Hongfei, et al.
Publicado: (2023)

Characteristics of autonomic dysfunction in neuronal intranuclear inclusion disease
por: Zhou, Lu, et al.
Publicado: (2023)

A Case Report of Sporadic Adult Neuronal Intranuclear Inclusion Disease (NIID) With Stroke-Like Onset
por: Lin, Pan, et al.
Publicado: (2020)

Longitudinal course of hyperintensity on diffusion weighted imaging in adult-onset neuronal intranuclear inclusion disease patients
por: Liu, Dan, et al.
Publicado: (2023)

Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions
por: Park, Hongsun, et al.
Publicado: (2022)

Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients
por: Park, Chang-Hun, et al.
Publicado: (2016)

A genetic screen of the mutations in the Korean patients with early-onset Alzheimer’s disease
por: An, Seong Soo, et al.
Publicado: (2016)

An Electron Microscope Study of Intranuclear Inclusions in Mouse Liver and Hepatoma
por: Leduc, Elizabeth H., et al.
Publicado: (1959)

Re‐defining the clinicopathological spectrum of neuronal intranuclear inclusion disease
por: Chen, Hao, et al.
Publicado: (2020)

No evidence supports the genetic heterogeneity of Neuronal intranuclear inclusion disease
por: Li, Hao, et al.
Publicado: (2020)

Temporal Changes in Brain Perfusion in Neuronal Intranuclear Inclusion Disease
por: Ataka, Takuya, et al.
Publicado: (2020)

Intranuclear birefringent inclusions in paraffin sections by polychromatic polarization microscopy
por: Vitkunaite, Aiste, et al.
Publicado: (2021)

Characteristic cerebral perfusion pattern in neuronal intranuclear inclusion disease
por: Tai, Hong-Fei, et al.
Publicado: (2022)

Unilateral Wing-Beating Tremor in Neuronal Intranuclear Inclusion Disease
por: Sugiyama, Atsuhiko, et al.
Publicado: (2023)

Rapidly progressive adult-onset neuronal intranuclear inclusion disease beginning with autonomic symptoms: a case report
por: Zhu, Yi, et al.
Publicado: (2023)

A GENERALIZED VISCERAL DISEASE OF GUINEA PIGS, ASSOCIATED WITH INTRANUCLEAR INCLUSIONS
por: Pappenheimer, Alwin M., et al.
Publicado: (1942)

An Autopsy Case of Familial Neuronal Intranuclear Inclusion Disease with Dementia and Neuropathy
por: Yamaguchi, Nanaka, et al.
Publicado: (2018)

Composition of the Intranuclear Inclusions of Fragile X-associated Tremor/Ataxia Syndrome
por: Ma, Lisa, et al.
Publicado: (2019)

Neuronal intranuclear inclusion disease with mental abnormality: a case report
por: Chi, Xiaosa, et al.
Publicado: (2020)

Reply to: No evidence supports genetic heterogeneity of neuronal intranuclear inclusion disease
por: Chen, Zhongbo, et al.
Publicado: (2020)

Neuropathy/intranuclear inclusion bodies in oculopharyngodistal myopathy: A case report
por: Matsubara, Tomoyasu, et al.
Publicado: (2021)

Genetic and Imaging Characteristics of a Family With Neuronal Intranuclear Inclusion Disease
por: Jung, Na-Yeon, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_r1hd3g4larfcaimqjfr2t2cs6u