Evidence map›Paper›PMID 40741087›Full record

ArticleAACE clinical case reports

SDHD Gene Mutations: Looking Beyond Head and Neck Tumors.

Sushma Kadiyala, Yasmin Khan, Valeria de Miguel, Megan N Frone, Fiemu Nwariaku, Jennifer Rabaglia, Stacey Woodruff, Elizabeth E King, Sumitha S Hathiramani, Karel Pacak and 1 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in AACE clinical case reports. 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
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.

  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

11 authors.

Sushma KadiyalaDepartment of Internal Medicine, Division of Endocrinology & Metabolism, University of Florida and the Malcolm Randall VA Medical Center, Gainesville, FL.
Yasmin KhanDepartment of Internal Medicine, Division of Endocrinology & Metabolism, University of Florida and the Malcolm Randall VA Medical Center, Gainesville, FL.
Valeria de MiguelEndocrinology Unit, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina, MD, USA.
Megan N FroneDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, DHHS, Bethesda, MD, USA.
Fiemu NwariakuDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, TX.
Jennifer RabagliaDepartment of Surgery, University of Texas Southwestern Medical Center, Dallas, TX.
Stacey WoodruffDepartment of Surgery, University of Hawaii John A. Burns School of Medicine, Honolulu, HI.
Elizabeth E KingEndocrine Associates of Dallas, Dallas, TX.
Sumitha S HathiramaniDepartiment of Internal Medicine, Division of Endocrinology & Metabolism, VA North Texas Healthcare System, Dallas, TX.
Karel PacakSection on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD.
Hans K GhayeeDepartment of Internal Medicine, Division of Endocrinology & Metabolism, University of Florida and the Malcolm Randall VA Medical Center, Gainesville, FL.

Funding

Intramural NIH HHS Z99 CA999999
6 · The paper itself

Abstract

Objective: Succinate dehydrogenase complex, subunit D ( Methods: We describe 2 cases of hereditary, early-onset, bilateral PCC/PGL syndrome associated with Results: Both cases presented under the age of 30 with bilateral PCC and PGL with Conclusion: While

Indexed as

Bilateral pheochromocytomasparagangliomaSDHD mutation

Identifiers

PMID40741087
PMCPMC12309827

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.