Advanced Biomedical Research
Author = Kolahdouz, Mahsa
Number of Articles: 3
Mutation detection of CYP21A2 gene in nonclassical congenital adrenal hyperplasia patients with premature pubarche
Volume 2016, March, March 2016, Pages 1-4
Mahsa Kolahdouz; Mahin Hashemipour; Hossein Khanahmad; Bahareh Rabbani; Mansoor Salehi; Ali Rabbani; Mona Mobalegh Naseri
Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia
Volume 2015, August, August 2015, Pages 1-5
Mahsa Kolahdouz; Zahra Mohammadi; Parisa Kolahdouz; Masoud Tajamolian; Hossein Khanahmad
Expression of prostaglandin I2 (prostacyclin) receptor in blood of migraine patients: A potential biomarker
Volume 2015, june, June 2015, Pages 1-4
Majid Kheirollahi; Mohammad Kazemi; Gilda A mini; Fariborz Khorvash; Fatemeh Ahangari; Mahsa Kolahdouz; Leila Koulivand
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