Evidence map›Paper›PMID 28509104›Full record

ArticleCEN case reports2015

Autosomal dominant distal renal tubular acidosis caused by a mutation in the anion exchanger 1 gene in a Japanese family.

Naoko Ito, Kenji Ihara, Tomohiro Kamoda, Satoshi Akamine, Kentaro Kamezaki, Noboru Tsuru, Ryo Sumazaki, Toshiro Hara

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in CEN case reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Distal renal tubular acidosis: genetic causes and management.World journal of pediatrics : WJP · 2019
    Review
  5. Renal Tubular Acidosis: HAdvances in chronic kidney disease · 2018
    Review
  6. Review
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

8 authors.

Naoko ItoDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8583, Japan. naokoito@pediatr.med.kyushu-u.ac.jp.
Kenji IharaDepartment of Pediatrics, Faculty of Medicine, Oita University, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Tomohiro KamodaDepartment of Pediatrics, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki, 305-8575, Japan.
Satoshi AkamineDepartment of Pediatrics, National Hospital Organization Kokura Medical Center, 10-1 Harugaoka, Kokuraminami-ku, Kitakyushu, Fukuoka, 802-8533, Japan.
Kentaro KamezakiDepartment of Pediatrics, National Hospital Organization Kokura Medical Center, 10-1 Harugaoka, Kokuraminami-ku, Kitakyushu, Fukuoka, 802-8533, Japan.
Noboru TsuruTsuru Noboru Clinic, 2-5-8 Hirao, Chuo-ku, Fukuoka, 810-0014, Japan.
Ryo SumazakiDepartment of Pediatrics, University of Tsukuba, 1-1-1 Tennoudai, Tsukuba, Ibaraki, 305-8575, Japan.
Toshiro HaraDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8583, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autosomal dominant distal renal tubular acidosis (dRTA) is a rare disorder caused by a mutation in the AE1 gene encoding the chloride-bicarbonate (Cl

Indexed as

Anion exchanger 1Autosomal dominantDistal renal tubular acidosisDominant negativeHypokalemiaSLC4A1

Identifiers

PMID28509104
PMCPMC5413770

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.