Evidence map›Paper›PMID 31750034›Full record

ArticleNeurology. Clinical practice2019

Adult-onset vocal cord paralysis in slow-channel congenital myasthenic syndrome.

Haruko Nakamura, Hiroyasu Komiya, Eri Uematsu, Yoshiharu Nakae, Kenichi Tanaka, Misako Kunii, Mikiko Tada, Hideto Joki, Shigeru Koyano, Naomichi Matsumoto and 3 more

Abstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Neurology. Clinical practice, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Haruko NakamuraDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Hiroyasu KomiyaDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Eri UematsuDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Yoshiharu NakaeDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Kenichi TanakaDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Misako KuniiDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Mikiko TadaDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Hideto JokiDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Shigeru KoyanoDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Naomichi MatsumotoDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Hiroshi DoiDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Hideyuki TakeuchiDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.
Fumiaki TanakaDepartment of Neurology and Stroke Medicine (HN, HK, EU, YN, KT, MK, MT, HJ, SK, HD, HT, FT) and Department of Human Genetics (NM), Yokohama City University Graduate School of Medicine, Fukuura, Kanazawa-ku, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID31750034
PMCPMC6814421

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.