I. Banerjee

Somatostatin receptors in congenital hyperinsulinism: Biology to bedside

S. Betz, K. Mohnike, M. Dunne, 2022, Frontiers in Endocrinology.

Likelihood of persistent GH deficiency into late adolescence: relationship to the presence of an ectopic or normally sited posterior pituitary gland

L. Patel, P. Murray, R. Amin, 2009, Clinical endocrinology.

Are Factors at Diagnosis of Growth Hormone Deficiency in Childhood Associated with Persistence of Growth Hormone Deficiency into Adult Life?

M. Scanlon, I. Banerjee, J. Gregory, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Congenital hyperinsulinism: management and outcome, a single tertiary centre experience

M. G. Shaikh, P. Robinson, I. Banerjee, 2020, European Journal of Pediatrics.

Osteogenesis imperfecta and intravenous pamidronate

J. Gregory, W. Evans, G. Shortland, 2002, Archives of disease in childhood.

Constitutional delay of growth and puberty is not commonly associated with mutations in the acid labile subunit gene.

D. Hanson, P. Clayton, A. Whatmore, 2008, European journal of endocrinology.

Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.

S. Mansour, D. Hanson, P. Clayton, 2012, Journal of molecular endocrinology.

Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.

S. Mansour, D. Hanson, S. Nampoothiri, 2012, Journal of Molecular Endocrinology.