Student or educator? Sign up with your school email and get 6 months of Pro free.
Cited by 221

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor

Open access
Dunne, Mark J., Kane, Charlotte, Shepherd, Ruth M., Sanchez, Jorge A., James, Roger F.L., Johnson, Paul R.V., Aynsley-Green, Albert, Lu, Shan, Clement, John P., Lindley, Keith J., Seino, Susumu, Aguilar-Bryan, Lydia, Gonzalez, Gabriela, Milla, Peter J.·1997·New England Journal of Medicine

Abstract

[1st paragraph] Persistent hyperinsulinemic hypoglycemia of infancy is caused by inappropriate and excessive secretion of insulin. Although the disease is rare in outbred communities (approximately 1 case per 50,000 persons), the incidence is approximately 1 per 2500 in inbred Arabic communities in which there is a familial (autosomal recessive) form of the disease. The disease most commonly presents with severe hypoglycemia a few hours after birth, although some cases present after several weeks or months. Some patients have a response to treatment with diazoxide or somatostatin, but others require partial pancreatectomy to control the hyperinsulinism.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1056/nejm199703063361005

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 2 references

Cited by

See all 221

Metadata

Authors
Dunne, M. J., Kane, C., Shepherd, R. M., Sanchez, J. A., James, R. F. L., Johnson, P. R. V., Aynsley-Green, A., Lu, S., Clement, J. P., Lindley, K. J., Seino, S., Aguilar-Bryan, L., Gonzalez, G., & Milla, P. J.
Venue
New England Journal of Medicine
Published
1997-03-06
Volume
336
Issue
10
Pages
703-706
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2095512900
Cited by
221
References
2
FWCI
24.51
Type
journal article
Language
en
Open access
bronze

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor. https://app.cochat.ai/papers/10.1056/nejm199703063361005
The paper
Dunne, M. J., Kane, C., Shepherd, R. M., Sanchez, J. A., James, R. F. L., Johnson, P. R. V., Aynsley-Green, A., Lu, S., Clement, J. P., Lindley, K. J., Seino, S., Aguilar-Bryan, L., Gonzalez, G., & Milla, P. J. (1997). Familial Persistent Hyperinsulinemic Hypoglycemia of Infancy and Mutations in the Sulfonylurea Receptor. New England Journal of Medicine. https://doi.org/10.1056/nejm199703063361005

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.