A. Mutair

Delayed hypoglycemic effect of insulin overdose in a diabetic child: a case report

A. Babiker, K. Noaim, A. Mutair, 2019, European Journal of Medical Case Reports.

Pediatric Giant Invasive Macroprolactinoma Presented as Pituitary Apoplexy

Ammar Ashraf, A. Mutair, A. Jabri, 2019 .

Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.

A. Hattersley, S. Ellard, A. Patch, 2009, The Journal of clinical endocrinology and metabolism.

Hypoparathyroidism–retardation–dysmorphism (HRD) syndrome in triplets

W. Eyaid, S. Saif, K. A. Al Tawil, 2005, American journal of medical genetics. Part A.

Patients' Perception of the Use of the EasyPod™ Growth Hormone Injector Device and Impact on Injection Adherence: A Multi-Center Regional Study

M. Savage, A. Deeb, N. Al Hassani, 2022, Frontiers in Pediatrics.

Newborn with dilated cardiomyopathy secondary to vitamin d deficiency.

A. Mutair, Hanan Al Azkawi, 2012 .

Four novel cases of permanent neonatal diabetes mellitus caused by homozygous mutations in the glucokinase gene

K. Hussain, C. James, H. Al-Shaikh, 2011, Pediatric diabetes.

Vitamin D deficient rickets: Not always nutritional

A. Mutair, Y. Binafif, 2017 .