A Japanese family with idiopathic basal ganglia calcification with novel SLC20A2 mutation presenting with late-onset hallucination and delusion.

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

11 citing papers in PubMed, 21 citations in OpenAlex.

1. The Genetics of Primary Familial Brain Calcification: A Literature Review.International journal of molecular sciences · 2023
   Review
2. Nosology and Phenomenology of Psychosis in Movement Disorders.Movement disorders clinical practice · 2020
   Review
3. Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response.Brain : a journal of neurology · 2019
   Article
4. On Neuropsychiatric Manifestations of Basal Ganglia Injury: A Report of Three Cases and Literature Review.Case reports in neurological medicine · 2019
   Article
5. A NovelChinese medical journal · 2018
   Article
6. Brain Calcification and Movement Disorders.Current neurology and neuroscience reports · 2017
   Review
7. Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid.Neurogenetics · 2016
   Article
8. Primary familial brain calcification: update on molecular genetics.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2015
   Article
9. The genetics of primary familial brain calcifications.Current neurology and neuroscience reports · 2014
   Review
10. Novel mutation of SLC20A2 in an Italian patient presenting with migraine.Journal of neurology · 2014
    Article
11. Genetic screening and functional characterization of PDGFRB mutations associated with basal ganglia calcification of unknown etiology.Human mutation · 2014
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

6 authors at 1 institution in 1 country.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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