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Author = Sade hal Setare
Number of Articles: 2
Alkaptonuria - an atypical manifestation or management?
Volume 11, Issue 6 , June 2023, , Pages 18013-18017
Abstract
Alkaptonuria is a rare autosomal recessive disease, in which the metabolism of homogentisic acid is defective. Homogentisate 1, 2- dioxygenase deficiency results in homogentisic aciduria, ... Read More
The Effect of Glucocorticoid therapy on Bone Mineral Density in Children and Adolescents with Congenital Adrenal Hyperplasia
Volume 9, Issue 10 , October 2021, , Pages 14569-14580