Evidence map›Paper›PMID 42441246›Full record

ArticleClinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology2026

A case of familial isolated hypoparathyroidism type 2 with novel compound heterozygous variants in

Nobuhiro Hashimoto, Yosuke Ichihashi, Hidekazu Sakai, Tairin Hiraizumi, Yukiko Mizutani, Shinichiro Sano, Mitsuhiro Nishida, Maki Fukami, Satoshi Narumi, Tsutomu Kamimaki and 1 more

Abstract read
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Article in Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology, 2026. 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

11 authors.

Nobuhiro HashimotoDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Yosuke IchihashiDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Hidekazu SakaiDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Tairin HiraizumiDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Yukiko MizutaniDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Shinichiro SanoDepartment of Diabetes and Metabolism, Shizuoka Children's Hospital, Shizuoka, Japan.
Mitsuhiro NishidaDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Maki FukamiDepartment of Molecular Endocrinology, National Center for Child Health and Development, Tokyo, Japan.
Satoshi NarumiDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
Tsutomu KamimakiDepartment of Pediatrics, Shizuoka City Shimizu Hospital, Shizuoka, Japan.
Tomonobu HasegawaDepartment of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

afebrile seizurefamilial isolated hypoparathyroidism type 2genetic diseaseglial cells missing homolog 2 (GCM2)hypocalcemia

Identifiers

PMID42441246
PMCPMC13337295

What OpenQuestion holds

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Registered trials

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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.