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Annals of Neurology|August 18, 2023
Distinct Patterns of Hippocampal Pathology in Alzheimer's Disease with Transactive Response DNA-binding Protein 43Grace Minogue, Allegra Kawles, Antonia Zouridakis, et al.Plos One|February 7, 2020
Using referral rates for genetic testing to determine the incidence of a rare disease: The minimal incidence of congenital hyperinsulinism in the UK is 1 in 28,389Daphne Yau, Thomas W Laver, Antonia Dastamani, et al.BMJ Open Diabetes Research & Care|January 8, 2020
Patterns of postmeal insulin secretion in individuals with sulfonylurea-treated KCNJ11 neonatal diabetes show predominance of non-KATP-channel pathwaysPamela Bowman, Timothy J McDonald, Bridget A Knight, et al.Acta Neuropathologica Communications|January 3, 2023
Differential vulnerability of the dentate gyrus to tauopathies in dementiasAllegra Kawles, Grace Minogue, Antonia Zouridakis, et al.Journal of the Endocrine Society|April 2, 2026
Comprehensive genetic rescreening improves diagnostic yield in congenital hyperinsulinismJonna M E Männistö, Jayne A L Houghton, Jasmin J Bennett, et al.European Journal of Endocrinology|April 2, 2014
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.Frontiers in Endocrinology|September 27, 2021
Molecular Genetics, Clinical Characteristics, and Treatment Outcomes of KATP-Channel Neonatal Diabetes Mellitus in Vietnam National Children's HospitalCan Thi Bich Ngoc, Tran Minh Dien, Elisa De Franco, et al.European Journal of Endocrinology|March 11, 2015
Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutationsHuseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, et al.The Journal of Clinical Endocrinology and Metabolism|October 20, 2009
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous familiesOscar Rubio-Cabezas, Ann-Marie Patch, Jayne A L Minton, et al.EMBO Molecular Medicine|January 6, 2010
Adjacent mutations in the gating loop of Kir6.2 produce neonatal diabetes and hyperinsulinismKenju Shimomura, Sarah E Flanagan, Brittany Zadek, et al.Pageof 51