Disease: Neuronal intranuclear inclusion disease
- <em>NOTCH2NLC</em> GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy
- A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids
- A case report of neuronal intranuclear inclusion disease (NIID) with MELAS-like imaging findings
- A case report of neuronal intranuclear inclusion disease onset with urinary incontinence
- A case report of neuronal intranuclear inclusion disease presenting with urinary incontinence
- A case report of neuronal intranuclear inclusion disease with paroxysmal peripheral neuropathy-like onset lacking typical signs on diffusion-weighted imaging
- A comment on a case report about perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode
- A comprehensive study of clinicopathological and genetic features of neuronal intranuclear inclusion disease
- A family with neuronal intranuclear inclusion disease with focal segmental glomerulosclerosis
- A patient with neuronal intranuclear inclusion disease combined with hypertension accompanied by elevated catecholamines
- A Rare Case of Suspected Neuronal Intranuclear Inclusion Disease Requiring Differentiation From Neuro-Behcet's Disease
- A rare stroke mimic: neuronal intranuclear inclusion disease
- Adult-onset neuronal intranuclear inclusion disease presenting with acute encephalitis-like episode and without characteristic hyperintensities on MR-DWI: a case report
- Adult-onset neuronal intranuclear inclusion disease related retinal degeneration: a Chinese case series
- Adult-type neuronal intranuclear inclusion disease with limb tremor onset: a case report
- Advances of NOTCH2NLC Repeat Expansions and Associated Diseases: A Bibliometric and Meta-analysis
- Aggregated Alpha-Synuclein Inclusions within the Nucleus Predict Impending Neuronal Cell Death in a Mouse Model of Parkinsonism
- Autonomic dysfunction-dominant phenotype in a Chinese family with biallelic GGC repeat expansions in NOTCH2NLC
- Blepharoptosis As an Early Manifestation of Neuronal Intranuclear Inclusion Disease
- Case report: Neuronal intranuclear inclusion disease initially mimicking reversible cerebral vasoconstriction syndrome: serial neuroimaging findings during an 11-year follow-up
- Case report: Neuronal intranuclear inclusion disease presenting with acute encephalopathy
- Characteristic cerebral perfusion pattern in neuronal intranuclear inclusion disease
- Characteristics of autonomic dysfunction in neuronal intranuclear inclusion disease
- Clinical and genetic analysis of a patient with Neuronal intranuclear inclusion body disease characterized by cortical enhancement in the posterior brain region
- Clinical and multimodal imaging features of adult-onset neuronal intranuclear inclusion disease
- Clinical characteristics of two patients with neuronal intranuclear inclusion disease and literature review
- Clinical Features and Classification of Neuronal Intranuclear Inclusion Disease
- Clinical features of neuronal intranuclear inclusion disease with seizures: a systematic literature review
- Clinical phenotypic diversity of <em>NOTCH2NLC</em>-related disease in the largest case series of inherited peripheral neuropathy in Japan
- Clinical-neuroimaging-pathological relationship analysis of adult onset Neuronal Intranuclear Inclusion Disease (NIID)
- Clinical, radiological, and molecular analyses of neuronal intranuclear inclusion disease with polyglycine inclusions
- CSF P-Tau181 and Other Biomarkers in Patients With Neuronal Intranuclear Inclusion Disease
- Current advances in neuronal intranuclear inclusion disease
- Diagnostic value of nerve conduction study in NOTCH2NLC-related neuronal intranuclear inclusion disease
- Diffuse argyrophilic grain disease with TDP-43 proteinopathy and neuronal intermediate filament inclusion disease: FTLD with mixed tau, TDP-43 and FUS pathologies
- Encephalitis-like episodes with cortical edema and enhancement in patients with neuronal intranuclear inclusion disease
- Expression of expanded GGC repeats within NOTCH2NLC causes behavioral deficits and neurodegeneration in a mouse model of neuronal intranuclear inclusion disease
- Expression of expanded GGC repeats within NOTCH2NLC causes cardiac dysfunction in mouse models
- First case of adult onset neuronal intranuclear inclusion disease with both typical radiological signs and NOTCH2NLC repeat expansions in a Caucasian individual
- General Anesthesia in a Patient With Neuronal Intranuclear Inclusion Disease: A Case Report
- Genetic Movement Disorders Commonly Seen in Asians
- GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation
- GGC repeat expansions in NOTCH2NLC cause uN2CpolyG cerebral amyloid angiopathy
- Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying <em>NOTCH2NLC</em> Repeat Expansion
- Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion
- Immune system involvement in neuronal intranuclear inclusion disease
- Intermediate-Length GGC Repeat Expansion in NOTCH2NLC Was Identified in Chinese Patients with Amyotrophic Lateral Sclerosis
- Letter to the editor on: Hornerin deposits in neuronal intranuclear inclusion disease: direct identification of proteins with compositionally biased regions in inclusions by Park et al. (2022)
- Longitudinal course of hyperintensity on diffusion weighted imaging in adult-onset neuronal intranuclear inclusion disease patients
- Loss of TDP-43 oligomerization or RNA binding elicits distinct aggregation patterns
- Mapping macrostructural and microstructural brain alterations in patients with neuronal intranuclear inclusion disease
- Microglia contribute to polyG-dependent neurodegeneration in neuronal intranuclear inclusion disease
- MRI Abnormalities Identify Neuronal Intranuclear Inclusion Disease
- MRI abnormalities identify Neuronal Intranuclear Inclusion Disease (NIID)
- MRI features of neuronal intranuclear inclusion disease, combining visual and quantitative imaging investigation
- MRI features of neuronal intranuclear inclusion disease, combining visual and quantitative imaging investigations
- Nerve conduction features may serve as a diagnostic clue for neuronal intranuclear inclusion disease
- Neuronal Intra-nuclear Inclusion Disease
- Neuronal intranuclear inclusion disease
- Neuronal intranuclear inclusion disease in a 66-year-old woman
- Neuronal intranuclear inclusion disease in New Zealand: A novel discovery
- Neuronal intranuclear inclusion disease mimicking progressive supranuclear palsy
- Neuronal intranuclear inclusion disease misdiagnosed as Parkinson's disease: a case report
- Neuronal intranuclear inclusion disease with cerebellar white matter tau uptake and incidental meningioma
- Neuronal intranuclear inclusion disease with cortical involvement in left hemisphere: a case report
- Neuronal intranuclear inclusion disease with multisystem involvement after long-term bladder dysfunction: a case report
- Neuronal intranuclear inclusion disease with neuroimaging mimicking MELAS
- Neuronal Intranuclear Inclusion Disease with NOTCH2NLC GGC Repeat Expansion: A Systematic Review and Challenges of Phenotypic Characterization
- Neuronal intranuclear inclusion disease: a case report and literature review
- Neuropathological features of adult-onset neuronal intranuclear inclusion disease with fluid-attenuated inversion recovery high-intensity signals in the cerebellar paravermal area from an early stage: A case report
- Not your usual neurodegenerative disease: a case report of neuronal intranuclear inclusion disease with unconventional imaging patterns
- NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment
- NOTCH2NLC mutation-positive neuronal intranuclear inclusion disease with retinal dystrophy: A case report and literature review
- Novel VCP activator reverses multisystem proteinopathy nuclear proteostasis defects and enhances TDP-43 aggregate clearance
- Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress
- Plasma neurofilament light as a promising biomarker in neuronal intranuclear inclusion disease
- Prevalence and Characterization of <em>NOTCH2NLC</em> GGC Repeat Expansions in Koreans: From a Hospital Cohort Analysis to a Population-Wide Study
- Proteomic profile of nuclei containing p62-positive inclusions in a patient with neuronal intranuclear inclusion disease
- Proximal sensory neuropathy and cerebellar ataxia as presenting symptoms of NOTCH2NLC-related neuronal intranuclear inclusion disease
- Rapidly progressive adult-onset neuronal intranuclear inclusion disease beginning with autonomic symptoms: a case report
- Rare genetic causes of meningitis and encephalitis
- Recent advances in CGG repeat diseases and a proposal of fragile X-associated tremor/ataxia syndrome, neuronal intranuclear inclusion disease, and oculophryngodistal myopathy (FNOP) spectrum disorder
- Recovery after Prolonged Disturbance of Consciousness and Repeated Cerebral Perfusion Changes in Neuronal Intranuclear Inclusion Disease
- Reversible encephalitis-like episodes in fragile X-associated tremor/ataxia syndrome: a case report
- Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease and NOTCH2NLC-Related GGC Repeat Expansion Disorders
- Skin biopsies for diagnosing neuronal intranuclear inclusion disease: A retrospective study of 12 cases
- Skin biopsy and neuronal intranuclear inclusion disease
- Temporal Changes in 18 F-FDG PET/CT in Familial Neuronal Intranuclear Inclusion Disease, Based on the Clinical Course
- Temporal Changes in 18F-FDG PET/CT in Familial Neuronal Intranuclear Inclusion Disease, Based on the Clinical Course
- The 5HT4R agonist velusetrag efficacy on neuropathic chronic intestinal pseudo-obstruction in PrP-SCA7-92Q transgenic mice
- The clinical characteristics of neuronal intranuclear inclusion disease and its relation with inflammation
- The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies
- The predominance of "astrocytic" intranuclear inclusions in neuronal intranuclear inclusion disease manifesting encephalopathy-like symptoms: A case series with brain biopsy
- Typical imaging manifestation of neuronal intranuclear inclusion disease in a man with unsteady gait: A case report
- Ultra-high-field 7-Tesla magnetic resonance imaging in fragile X tremor/ataxia syndrome (FXTAS)
- Unilateral Hemispheric Edema and Hyperperfusion in Neuronal Intranuclear Inclusion Disease
- Unilateral Wing-Beating Tremor in Neuronal Intranuclear Inclusion Disease
- Unraveling rare form of adult-onset NIID by characteristic brain MRI features: A single-center retrospective review
- Utility of labial salivary gland biopsy in the histological diagnosis of neuronal intranuclear inclusion disease
- Value of neutrophil-to-lymphocyte ratio in neuronal intranuclear inclusion disease