E. Heffernan

A novel IGSF1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF1 deficiency syndrome

M. Dattani, O. Koulouri, M. Gurnell, 2018, Clinical endocrinology.

mutation in a large Irish kindred highlights the need for familial 1 screening in the IGSF 1 deficiency syndrome 2

M. Dattani, O. Koulouri, M. Gurnell, 2018 .

Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study

Kenneth L. Jones, A. Hattersley, S. Ellard, 2018, The lancet. Diabetes & endocrinology.

G104(P) Audit of Endocrine Late Effects in Survivors of Childhood Brain Tumours

R. Johnston, S. Koppikar, A. McCarthy, 2012, Archives of Disease in Childhood.

Infant with macroglossia

P. Mallett, E. Heffernan, Kathryn Mullan, 2024, Archives of Disease in Childhood.