Cargando…

A comment on a case report about perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode

Detalles Bibliográficos
Autor principal:	Finsterer, Josef
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9918409/ https://www.ncbi.nlm.nih.gov/pubmed/36785597 http://dx.doi.org/10.1016/j.cccb.2023.100160

Ejemplares similares

Perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode: A case report
por: Kutsuna, Fumiya, et al.
Publicado: (2022)

Neuronal intranuclear inclusion disease presenting with an MELAS-like episode in chronic polyneuropathy
por: Ishihara, Tasuku, et al.
Publicado: (2020)

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

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

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

Adult-Onset Neuronal Intranuclear Inclusion Disease with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like (MELAS-like) Episode: A Case Report and Review of Literature
por: Zhou, Qian, et al.
Publicado: (2022)

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

Encephalitic Episodes Followed by Leukoencephalopathy: A Novel Indication for Neuronal Intranuclear Inclusion-Body Disease
por: Zhou, Liche, et al.
Publicado: (2020)

Stroke and Stroke-like Episodes in Muscle Disease
por: Finsterer, Josef
Publicado: (2012)

Genetic heterogeneity of neuronal intranuclear inclusion disease: What about the infantile variant?
por: Sikora, Jakub, et al.
Publicado: (2021)

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

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

Consider Stroke-Like Episodes as a Differential of Migrainous Stroke
por: Finsterer, Josef
Publicado: (2020)

Reply: Genetic heterogeneity of neuronal intranuclear inclusion disease. What about the infantile variant?
por: Yau, Wai Yan, et al.
Publicado: (2021)

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

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)

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

Case report: Neuronal intranuclear inclusion disease presenting with acute encephalopathy
por: Bu, Julia Ting, et al.
Publicado: (2023)

A case of neuronal intranuclear inclusion disease associated with lupus nephritis–like nephropathy
por: Horino, Taro, et al.
Publicado: (2018)

Antiepileptics and NO-precursors may be beneficial for stroke-like episodes
por: Finsterer, Josef
Publicado: (2018)

Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging
por: Kikumoto, Mai, et al.
Publicado: (2021)

Neuronal intranuclear inclusion disease mimicking acute cerebellitis: A case report
por: Guo, Jiao-Jiao, et al.
Publicado: (2020)

Neuronal Intranuclear Inclusion Disease-Related Neurotrophic Keratitis: A Case Report
por: Liu, Pei, et al.
Publicado: (2022)

Therapeutic management of stroke-like episodes varies from that of encephalitis
por: Finsterer, Josef
Publicado: (2020)

Consider Stroke-Like Episodes as a Differential in Children with Acute Hemiparesis
por: Finsterer, Josef
Publicado: (2019)

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

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)

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

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

Neuronal intranuclear inclusion disease presented with recurrent vestibular migraine-like attack: a case presentation
por: Zhao, Danhua, et al.
Publicado: (2021)

A case of neuronal intranuclear inclusion disease with recurrent vomiting and without apparent DWI abnormality for the first seven years
por: Okamura, Shun, et al.
Publicado: (2020)

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

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

Familial frontotemporal dementia with neuronal intranuclear inclusions is not a polyglutamine expansion disease
por: Mackenzie, Ian R, et al.
Publicado: (2006)

A beneficial effect of l-arginine for stroke-like episodes is currently unsupported
por: Finsterer, Josef, et al.
Publicado: (2018)

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

Imaging findings and pathological correlations of subacute encephalopathy with neuronal intranuclear inclusion disease–Case report
por: Mori, Koichiro, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_qq2cvqh2u5cmn2qe27gq2hvb55