ArticleNeurogenetics2014
Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification.
Article in Neurogenetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 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
10 citing papers in PubMed, 21 citations in OpenAlex.
- A case report of a patient with primary familial brain calcification with aFrontiers in neurology · 2023Article
- Mechanisms of calcification in Fahr disease and exposure of potential therapeutic targets.Neurology. Clinical practice · 2020Review
- Primary brain calcification: an international study reporting novel variants and associated phenotypes.European journal of human genetics : EJHG · 2018Article
- A NovelChinese medical journal · 2018Article
- Clinical and radiological diversity in genetically confirmed primary familial brain calcification.Scientific reports · 2017Article
- Deciphering the causes of sporadic late-onset cerebellar ataxias: a prospective study with implications for diagnostic work.Journal of neurology · 2017Observational
- Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid.Neurogenetics · 2016Article
- Primary familial brain calcification in a Norwegian family, caused by a novel SLC20A2 gene mutation.Journal of neurology · 2016Article
- First report of a de novo mutation at SLC20A2 in a patient with brain calcification.Journal of molecular neuroscience : MN · 2014Article
- Novel mutation of SLC20A2 in an Italian patient presenting with migraine.Journal of neurology · 2014Article
Corrections and comments
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Authors and funding
13 authors at 6 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
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.