A novel mutation in the proopiomelanocortin (POMC) gene of a Hispanic child: metformin treatment shows a beneficial impact on the body mass index

A novel MC4R mutation associated with childhood-onset obesity: A case report

(2017) Manpreet Doulla et al.   Paediatrics & Child Health

Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist

(2016) Peter Kühnen et al.   NEW ENGLAND JOURNAL OF MEDICINE

The melanocortin system and insulin resistance in humans: insights from a patient with complete POMC deficiency and type 1 diabetes mellitus

(2013) I R Aslan et al.   INTERNATIONAL JOURNAL OF OBESITY

A novel missense mutation in the signal peptide of the human POMC gene: a possible additional link between early-onset type 2 diabetes and obesity

(2012) Monica Mencarelli et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Isolated cortisol deficiency: A rare cause of neonatal cholestasis

(2012) Abdulrahman Al-Hussaini et al.   Saudi Journal of Gastroenterology

Metformin for Obesity in Children and Adolescents: A Systematic Review

(2009) M. H. Park et al.   DIABETES CARE

Unexpected Endocrine Features and Normal Pigmentation in a Young Adult Patient Carrying a Novel Homozygous Mutation in the POMC Gene

(2008) Karine Clément et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM