Shirin Moarefian
Overview
Explore the profile of Shirin Moarefian including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
2
Citations
6
Followers
0
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Recent Articles
1.
Alaee M, Saneifard H, Shakiba M, Hanifeh M, Moarefian S
Clin Case Rep
. 2025 Feb;
13(2):e70170.
PMID: 39973892
Galactosemia is a rare autosomal recessive metabolic disorder with four main types, and classic galactosemia is the most prevalent. These patients have galactose-1-phosphate-uridyltransferase deficiency. We report on a case of...
2.
Moarefian S, Zamani M, Rahmanifar A, Behnam B, Zaman T
JIMD Rep
. 2022 Apr;
63(3):231-239.
PMID: 35433176
Citrullinemia type 1 is an autosomal recessive metabolic disease caused by gene mutations encoding argininosuccinic acid synthetase enzyme which is within the pathway of arginine and nitric oxide biosynthesis. Disease...
3.
Sheikhmoonesi F, Shafaat A, Moarefian S, Zaman T
Iran J Pediatr
. 2013 Jun;
23(2):245-6.
PMID: 23724196
No abstract available.