Angham N. Al Mutair
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 9 publications
Resolved Severe Primary Hypothyroidism in Sensenbrenner Syndrome Post Hepatorenal Transplantation: A Case Report.
Journal: Hormone research in paediatrics
Published: June 24, 2022
Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy
Journal: Journal of clinical research in pediatric endocrinology
Published: July 10, 2019
Growth hormone therapy and treatment outcomes: current clinical practice of the Gulf Cooperation Council.
Journal: Expert review of endocrinology & metabolism
Published: July 01, 2014
Heterogeneity in phenotype of usher-congenital hyperinsulinism syndrome: hearing loss, retinitis pigmentosa, and hyperinsulinemic hypoglycemia ranging from severe to mild with conversion to diabetes.
Journal: Diabetes care
Published: November 15, 2012
Mutation of the CYP2R1 vitamin D 25-hydroxylase in a Saudi Arabian family with severe vitamin D deficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 03, 2012
Puberty development among children and adolescents with chronic disease in Saudi Arabia.
Journal: Annals of Saudi medicine
Published: June 19, 2012
Newborn with dilated cardiomyopathy secondary to vitamin d deficiency.
Journal: Case reports in pediatrics
Published: May 27, 2012
Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: March 09, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026