الدكتور براتك شاه

Shah, P., et al., 2016. - Review article on "Hyperinsulinaemic Hypoglycaemia in Children and Adults". Lancet Diabetes and Endocrinology. (unpublished - currently with reviewers). 

Gevers, E. F., Meredith, S., Shah, P., Torpiano, J., Peters, C., Sebire, N.J., Slater, O., White, A.,  Dattani. M.H., 2016. Cushing Syndrome in a 2 year old child due to Pro-opiomelanocortin (POMC) secretion from a yolk sac turnour. (unpublished — currently being reviewed European Journal of Endocrinology). 

Improda, N., Shah, P., Güemes, M., Gilbert, C., Morgan, K., Sebire, N., Bockenhauer, D., Hussain, K., 2016. Hepatocyte nuclear factor 4 alfa (HNF4A) mutation associated to hyperinsulinaemic hypoglycaemia and atypical renal Fanconi syndrome: expanding the clinical phenotype. Accepted Horm Res Paediatr. 

Güemes, M., Shah, P., Roženková, K., Gilbert, C., Morgan, K., Hussain, K., 2016. Severe Hyperinsulinaemic Hypoqlycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 1 Ip15.5 Manaqed with Sirolimus Therapv. Horm Res Paediatr.

Shah, P., Rahman, S.A., McElroy, S., Gilbert, C., Morgan, K., Hinchey, L., Senniappan, S., Levy, H., Amin, R., Hussain, K., 2015. Use of Lonq-Actinq Somatostatin Analogue (Lanreotide) in an Adolescent with Diazoxide-Responsive Congenital Hyperinsulinism and Its Psycholoqical Impact. Horm Res Paediatr. 

Roženková, K., Güemes, M., Shah, P., Hussain, K., 2015. The Diagnosis and Management of Hvperinsulinaemic Hvpoqlvcaemia. J Clin Res Pediatr Endocrinol. 7:2. Pp. 86-97. 

Senniappan, S., Pitt, K., Shah, P., Arya, V., Jaiswal, S., Haddad, M., Hind, J., Dhawan, A., Davenport, M., Hussain, K., 2015. Postprandial Hyperinsulinaemic Hypoglycaemia Secondary to a Congenital Portosystemic Shunt. Horm Res Paediatr. 

Shah, P., Arya, V.B., Flanaaan, S.E., Morgan, K., Ellard, S., Senniappan, S., Hussain, H., 2014. Sirolimus therapy in a patient with severe hyperinsulinaemic hypoglycaemia due to a compound heterozygous ABCC8 gene mutation. J Pediatr Endocrinol Metab. Demirbilek, H., Tahir, S., Baran, R.T., Sherif, M., Shah, P., Ozbek, M.N., Hatipoglu, N., Baran, A., Arya, V.B., Hussain, K., 2014. Familial Isolated Growth Hormone Deficiency Due to A Novel Homozygous Missense Mutation in the Growth Hormone Releasinq Hormöne Receptor Gene: Clinical Presentation with Hypoqlycaemia. J Clin Endocrinol Metab.

Arya, V.B., Guemes, M., Nessa, A., Alam, S., Shah, P., Gilbert, C., Senniappan, S., Flanagan, S.E., Ellard, S., Hussain, K., 2014. Clinical and Histoloqical Heterogeneity of Conqenital Hyperinsulinism due to Paternally Inherited Heterozygous ABCC8/KCNJ11 Mutations. Eur J Endocrinol.