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Paediatrics & Child Health|May 3, 2021
Preschool autism services: A tale of two Canadian provinces and the implications for policyIsabel M Smith, Charlotte Waddell, Wendy J Ungar, et al.
Molecular Genetics & Genomic Medicine|April 3, 2021
Founder mutation in the PMM2 promotor causes hyperinsulinemic hypoglycaemia/polycystic kidney disease (HIPKD)Sumaya Islam, Mehmet Tekman, Sarah E Flanagan, et al.
European Journal of Endocrinology|September 10, 2014
Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutationsVed Bhushan Arya, Maria Guemes, Azizun Nessa, et al.
Diabetes Care|May 14, 2009
Tooth discoloration in patients with neonatal diabetes after transfer onto glibenclamide: a previously unreported side effectJanani Kumaraguru, Sarah E Flanagan, Siri Atma W Greeley, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 24, 2025
Basic Science and PathogenesisHaritha Vardhini Katragadda, Ali Ghaseminejad-Bandpey, Mallory Keating, et al.
World Neurosurgery|July 30, 2019
Infratentorial Glioblastoma Metastasis to BoneJocelyn A Ricard, Samuel W Cramer, River Charles, et al.
Journal of Abnormal Psychology|August 30, 2008
Motivational pathways to alcohol use and abuse among Black and White adolescentsM Lynne Cooper, Jennifer L Krull, V Bede Agocha, et al.
Neurology|July 27, 2007
A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brainK Shimomura, F Hörster, H de Wet, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 27, 2014
Chromosome 6q24 transient neonatal diabetes mellitus and protein sensitive hyperinsulinaemic hypoglycaemiaPrabhakaran Kalaivanan, Ved Bhushan Arya, Pratik Shah, et al.
Nucleic Acids Research|May 4, 2004
DNA binding and antigene activity of a daunomycin-conjugated triplex-forming oligonucleotide targeting the P2 promoter of the human c-myc geneGiuseppina M Carbone, Eileen McGuffie, Sara Napoli, et al.
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