Evidence map›Paper›PMID 37564608›Full record

ArticleClinical case reports2023

A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids.

Keisuke Morita, Takahiro Shinzato, Yuzo Endo, Makoto Suzuki, Hidefumi Yoshida, Jun Sone, Kojiro Nagai

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Adult-onset neuronal intranuclear inclusion disease presenting with acute encephalitis-like episode and without characteristic hyperintensities on MR-DWI: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  6. Article
  7. 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

7 authors at 2 institutions in 1 country.

Keisuke MoritaDepartment of Nephrology Shizuoka General Hospital Shizuoka Japan.
Takahiro ShinzatoDepartment of Nephrology Shizuoka General Hospital Shizuoka Japan.
Yuzo EndoDepartment of Diagnostic Pathology Shizuoka General Hospital Shizuoka Japan.
Makoto SuzukiDepartment of Diagnostic Pathology Shizuoka General Hospital Shizuoka Japan.
Hidefumi YoshidaDepartment of Neurology Shizuoka General Hospital Shizuoka Japan.
Jun SoneDepartment of Neuropathology, Institute for Medical Science of Aging Aichi Medical University Aichi Japan.
Kojiro NagaiDepartment of Nephrology Shizuoka General Hospital Shizuoka Japan.ORCID https://orcid.org/0000-0002-8348-2855
Shizuoka General Hospital · JPAichi Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuronal intranuclear inclusion disease (NIID) is a progressive neurodegenerative disorder characterized by intranuclear inclusions. Kidney injury involvement and successful treatment for NIID have rarely been reported. A NIID patient developed crescentic IgA nephropathy. Steroid therapy resolved digestive symptoms and recovered renal function. Steroids are considered for concomitant symptoms of NIID.

Indexed as

crescentic nephritisfibroblastIgA nephropathyneuronal intranuclear inclusion diseasesteroids

Identifiers

PMID37564608
PMCPMC10410123
OpenAlexW4385706456

What OpenQuestion holds

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LicenceCC BY
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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.