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First report on the use of pasireotide in a case of severe congenital hyperinsulinism due to a homozygous ABCC8 mutation

Overview of attention for article published in this source, May 2021
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5 Mendeley
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Title
First report on the use of pasireotide in a case of severe congenital hyperinsulinism due to a homozygous ABCC8 mutation
Published by
Korean Society of Pediatric Endocrinology, May 2021
DOI 10.6065/apem.2142010.005
Pubmed ID
Authors

Christiaan F. Mooij, Carline E. Tacke, Mirjam E. van Albada, Winfried Barthlen, Hennie Bikker, Klaus Mohnike, Matthijs W.N. Oomen, A.S. Paul van Trotsenburg, Nitash Zwaveling-Soonawala

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 20%
Unknown 4 80%
Readers by discipline Count As %
Pharmacology, Toxicology and Pharmaceutical Science 1 20%
Unknown 4 80%