M. Sherif

Dipeptidyl peptidase-4 expression in pancreatic tissue from patients with congenital hyperinsulinism.

K. Hussain, S. Senniappan, S. Rahman, 2015, International journal of clinical and experimental pathology.

A novel homozygous SLC19A2 mutation in a Portuguese patient with diabetes mellitus and thiamine-responsive megaloblastic anaemia

K. Hussain, A. Morais, L. Leijssen, 2015, International Journal of Pediatric Endocrinology.

Familial isolated growth hormone deficiency due to a novel homozygous missense mutation in the growth hormone releasing hormone receptor gene: clinical presentation with hypoglycemia.

K. Hussain, M. Ozbek, H. Demirbilek, 2014, The Journal of clinical endocrinology and metabolism.

A novel ALMS1 homozygous mutation in two Turkish brothers with Alström syndrome

A. Çayır, K. Hussain, S. Rahman, 2016, Journal of pediatric endocrinology & metabolism : JPEM.

Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis

A. Çayır, B. Cavdarli, K. Hussain, 2020, Journal of clinical research in pediatric endocrinology.