Evidence map›Paper›PMID 31363477›Full record

ArticleWorld journal of clinical cases2019

Longitudinal observation of ten family members with idiopathic basal ganglia calcification: A case report.

Seiju Kobayashi, Kumiko Utsumi, Masaru Tateno, Tomo Iwamoto, Tomonori Murayama, Hitoshi Sohma, Wataru Ukai, Eri Hashimoto, Chiaki Kawanishi

Open access · diamondAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in World journal of clinical cases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 88% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

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

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Seiju KobayashiShinyukai Nakae Hospital, Sapporo 0010022, Japan. seij@pastel.ocn.ne.jp.
Kumiko UtsumiDepartment of Psychiatry, Sunagawa City Medical Center, Sunagawa 0730196, Japan.
Masaru TatenoTokiwa Child Development Center, Tokiwa Hospital, Sapporo, Japan, Department of Neuropsychiatry, Sapporo Medical University Graduate School of Medicine, Sapporo 0050853, Japan.
Tomo IwamotoDepartment of Neuropsychiatry, Sapporo Medical University Graduate School of Medicine, Sapporo 0608543, Japan.
Tomonori MurayamaDepartment of Neuropsychiatry, Sapporo Medical University Graduate School of Medicine, Sapporo 0608543, Japan.
Hitoshi SohmaDepartment of Educational Development, Sapporo Medical University Center for Medical Education, Sapporo 0608543, Japan.
Wataru UkaiDepartment of Educational Development, Sapporo Medical University Center for Medical Education, Sapporo 0608543, Japan.
Eri HashimotoDepartment of Neuropsychiatry, Sapporo Medical University Graduate School of Medicine, Sapporo 0608543, Japan.
Chiaki KawanishiDepartment of Neuropsychiatry, Sapporo Medical University Graduate School of Medicine, Sapporo 0608543, Japan.
Sapporo Medical University · JPKeiyukai Sapporo Hospital · JPSapporo Higashi Tokushukai Hospital · JPSunagawa City Medical Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFamilial idiopathic basal ganglia calcification (FIBGC) is a rare autosomal dominant disorder that causes bilateral calcification of the basal ganglia and/or cerebellar dentate nucleus, among other locations. CASE SUMMARY: The aim of this study is to report 10 cases of FIBGC observed in a single family. Seven patients showed calcification on their computed tomography scan, and all of these patients carried the

conclusionThe accumulation of more case reports and further studies related to the manifestation of FIBGC are needed.

Indexed as

Case reportDiffuse neurofibrillary tangles with calcificationFahr’s diseaseIdiopathic basal ganglia calcificationSingle-photon emission computed tomographySLC20A2

Identifiers

PMID31363477
PMCPMC6656673
OpenAlexW2954675787

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

None linked

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.