Author = Hovsepian, Sylvia
R434X Mutation in Dual Oxidase 2 Gene among Patients with Permanent and Transient Congenital Hypothyroidism

Volume 30, Issue 211, September and October 2013, Pages 1745-1752

Omid Khoshnoud; Mohammad Hassan Tajaddini; Mahin Hashemipour; Mansour Salehi; Awat Feizi; Shaghayegh Haghjooy Javanmard; Roya Kelishadi; Silva Hovsepian; Masoud Amini


The Relation between Serum and Filter Paper thyroid-Stimulating HormoneLevels in Neonates with Congenital Hypothyroidism

Volume 30, Issue 205, July and August 2012

Ali Hassan Ayyad; Mahmoud Ghasemi; Mahin Hashemipour; Ali Mehrabi Kooshki; Silva Hovsepian; Mahmoud Afshari


The Mutation of Dual Oxidase 2 (DUOX2) Gene among Patients with Permanent and Transient Congenital Hypothyroidism

Volume 29, Issue 139, March and April 2011, Pages 588-595

Nooshin Rostampour; Mohamadhasan Tajaddini; Mahin Hashemipour; Mansour Salehi; Avat Feizi; Shaghayegh Haghjooy Javanmard; Roya Kelishadi; Hosein Saneian; Silva Hovsepian; Massoud Amini


Congenital Hypothyroidism; is There any Familial Component?

Volume 27, Issue 94, March and April 2009, Pages 135-142

Nasibeh Hasani; Bahar Dehghan; Masood Amini; Kamal Heidari; Ali Sajadi; Ali Ajami; Masoomeh Dastanpour; Rezvaneh Hadian; Ashraf Aminoroaya; Zahra Pournaghshband; Silva Hovsepian; Mahin Hashemipour


Does the Prevalence of Hearing Impairment ِDiffer in Children with Congenital Hypothyroidism and Healthy Children in Isfahan?

Volume 25, Issue 87, September and October 2008

Mehdi Salek; Mahin Hashemipour; Mostafa Hashemi; Mahsa Hajrahimi; Somayeh Sadeghi; Ziba Farajzadegan; Sylvia Hovsepian; Rezvaneh Hadian