ArticleBrain : a journal of neurology2018
POLR3A variants in hereditary spastic paraplegia and ataxia.
Article in Brain : a journal of neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 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
16 citing papers in PubMed, 22 citations in OpenAlex.
- A scoping review of stem cell models of leukodystrophies: advances in understanding pathophysiological mechanisms.NPJ genomic medicine · 2025Article
- Phenotypic Variability in ATP13A2 Mutations: The First Report of SPG78 From India.Journal of movement disorders · 2025Article
- Stress and Quality of Life of Parents of Children With POLR3-Related Leukodystrophy: A Cross-Sectional Pilot Study.Journal of child neurology · 2025Article
- POLR3A-related disorders: expanding the clinical phenotype.Journal of neurology · 2024Article
- Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants inJournal of medical genetics · 2023Article
- Spectrum of Pediatric to Early AdulthoodMovement disorders clinical practice · 2023Article
- Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia.Neuropathology : official journal of the Japanese Society of Neuropathology · 2022Article
- Importance of lipids for upper motor neuron health and disease.Seminars in cell & developmental biology · 2021Review
- Challenges and Controversies in the Genetic Diagnosis of Hereditary Spastic Paraplegia.Current neurology and neuroscience reports · 2021Review
- RNA Polymerase III Subunit Mutations in Genetic Diseases.Frontiers in molecular biosciences · 2021Review
- POLR3-related leukodystrophy: How do mutations affecting RNA polymerase III subunits cause hypomyelination?Faculty reviews · 2021Review
- POLR3A variants with striatal involvement and extrapyramidal movement disorder.Neurogenetics · 2020Article
- POLR3A-related spastic ataxia: new mutations and a look into the phenotype.Journal of neurology · 2020Article
- Clinical spectrum of POLR3-related leukodystrophy caused by biallelicNeurology. Genetics · 2019Article
- Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.Brain : a journal of neurology · 2019Article
- Reply: POLR3A variants in hereditary spastic paraplegia and ataxia.Brain : a journal of neurology · 2018Article
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Authors and funding
17 authors at 9 institutions in 3 countries.
Funding
Abstract
PubMed holds no abstract for this paper.
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What 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.