ArticleBrain : a journal of neurology2020
Essential phenotypes of NOTCH2NLC-related repeat expansion disorder.
Article in Brain : a journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 15 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
15 citing papers in PubMed.
- Microglia contribute to polyG-dependent neurodegeneration in neuronal intranuclear inclusion disease.Acta neuropathologica · 2024Article
- Mapping macrostructural and microstructural brain alterations in patients with neuronal intranuclear inclusion disease.Neuroradiology · 2024Article
- Review of Phenotypic Heterogeneity of Neuronal Intranuclear Inclusion Disease andNeurology. Genetics · 2024Review
- Nerve conduction features may serve as a diagnostic clue for neuronal intranuclear inclusion disease.Brain communications · 2024Article
- Current advances in neuronal intranuclear inclusion disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2023Review
- NOTCH2NLC-related oculopharyngodistal myopathy type 3 complicated with focal segmental glomerular sclerosis: a case report.BMC neurology · 2022Article
- The CGG repeat expansion in RILPL1 is associated with oculopharyngodistal myopathy type 4.American journal of human genetics · 2022Article
- Clinical and mechanism advances of neuronal intranuclear inclusion disease.Frontiers in aging neuroscience · 2022Review
- Case report: Two siblings with neuronal intranuclear inclusion disease exhibiting distinct clinicoradiological findings.Frontiers in neurology · 2022Article
- NOTCH2NLC-related repeat expansion disorders: an expanding group of neurodegenerative disorders.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021Review
- The GGC repeat expansion in NOTCH2NLC is associated with oculopharyngodistal myopathy type 3.Brain : a journal of neurology · 2021Article
- GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy.Annals of clinical and translational neurology · 2021Article
- Neuronal intranuclear inclusion disease: recognition and update.Journal of neural transmission (Vienna, Austria : 1996) · 2021Review
- GGC Repeat Expansion in theFrontiers in genetics · 2021Article
- Screening GGC repeat expansion in theAlzheimer's & dementia (Amsterdam, Netherlands)Article
Corrections and comments
- Comment on
- Erratum issuedErratum.2020
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
31886491What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.