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Diabetes|July 7, 2022
Effects of GLP-1 and GIP on Islet Function in Glucose-Intolerant, Pancreatic-Insufficient Cystic FibrosisSarah C Nyirjesy, Amy J Peleckis, Jack N Eiel, et al.
Annals of Neurology|October 1, 1996
Exclusion of the DYT1 locus in familial torticollisS B Bressman, T T Warner, L Almasy, et al.
Med (New York, N.Y.)|March 19, 2025
Global, multi-center, repeat-dose, phase 2 study of RZ358 (ersodetug), an insulin receptor antibody, for congenital hyperinsulinismHuseyin Demirbilek, Maria Melikyan, Violeta Iotova, et al.
Hormone Research in Paediatrics|July 16, 2023
International Guidelines for the Diagnosis and Management of HyperinsulinismDiva D De Leon, Jean Baptiste Arnoux, Indraneel Banerjee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 1, 2019
Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and managementSarah E Sheppard, Emilie Lalonde, N Scott Adzick, et al.
Nature Genetics|September 1, 1997
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding proteinL J Ozelius, J W Hewett, C E Page, et al.
Frontiers in Endocrinology|May 19, 2025
Developing a congenital hyperinsulinism prioritized research agenda: a patient-driven international collaborative research networkTai L S Pasquini, Indraneel Banerjee, Henrik Thybo Christesen, et al.
Ebiomedicine|May 25, 2026
Low-level mosaic variants causing the pancreatic disease congenital hyperinsulinism can be detected from blood DNAJasmin J Bennett, Thomas W Laver, Jonna M E Männistö, et al.
Annals of Neurology|October 24, 1997
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite familiesL Almasy, S B Bressman, D Raymond, et al.
Genome Research|May 1, 1997
Fine localization of the torsion dystonia gene (DYT1) on human chromosome 9q34: YAC map and linkage disequilibriumL J Ozelius, J Hewett, P Kramer, et al.
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