Author = Mahin Hashemipour
Number of Articles: 16

Evaluation of growth hormone deficiency in children with cystic fibrosis

Volume 2022, july, Summer 2022, Pages 1-4

Mohsen Reisi, Niloufar Sharif Ahmadian, Mahin Hashemipour, Neda Mostofizadeh, Majid Keivanfar, Elham Hashemi

Cardiovascular risk factors in children and adolescents with congenital adrenal hyperplasia

Volume 2021, july, July 2021, Pages 1-6

Elham Hashemi Dehkordi, Sara Khaheshi, Neda Mostofizadeh, Mahin Hashemipour

Genetic Study of Hepatocyte Nuclear Factor 1 Alpha Variants in Development of Early-Onset Diabetes Type 2 and Maturity-Onset Diabetes of the Young 3 in Iran

Volume 2019, september, September 2019, Pages 1-8

Aliasgar Mohammadi, Ameneh Eskandari, Akram Sarmadi, Mehrali Rahimi, Bijan Iraj, Mahin Hashemipour, Morteza Hashmezadeh Chaleshtori, Mohammad Amin Tabatabaiefar

SOFT Syndrome: The First Case in Iran

Volume 2018, september, September 2018, Pages 1-5

Neda Mostofizadeh, Mahshid Gheidarloo, Mahin Hashemipour, Elham Hashemi Dehkordi

Twin Brothers with Carnitine Membrane Transporter Deficiency: A Case Study

Volume 2018, july, July 2018, Pages 1-5

Elham Hashemi Dehkordi, Payam Sobhani, Nabiolah Asadpour, Mahin Hashemipour, Neda Mostofizadeh

Thrombotic Thrombocytopenic Purpura in a Child with Diabetic Ketoacidosis

Volume 2018, February, February 2018, Pages 1-3

Neda Mostofizadeh, Serajaddin Arefnia, Mahin Hashemipour, Elham Hashemi Dehkordi

A Case of Tyrosinemia Type III with Status Epilepticus and Mental Retardation

Volume 2018, January, January 2018, Pages 1-3

Reza Najafi, Neda Mostofizadeh, Mahin Hashemipour

Homocystinuria with Stroke and Positive Familial History

Volume 2017, october, October 2017, Pages 1-4

Ali Mazaheri, Neda Mostofizadeh, Mahin Hashemipour

Analysis of the T354P mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis

Volume 2016, April, April 2016, Pages 1-4

Hajar Miranzadeh-Mahabadi, Modjtaba Emadi-Baygi, Parvaneh Nikpour, Neda Mostofizade, Silva Hovsepian, Mahin Hashemipour

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

Glycemic index, glycemic load and childhood obesity: A systematic review

Volume 2014, January, January 2014, Pages 1-8

Mohammad Hossein Rouhani, Roya Kelishadi, Mahin Hashemipour, Ahmad Esmaillzadeh, Leila Azadbakht

The relation between serum and filter paper TSH level in neonates with congenital hypothyroidism

Volume 2014, January, January 2014, Pages 1-5

Ali Hassan Ayyad, Mahin Hashemipour, Silva Hovsepian, Ali Mehrabi Kooshki, Mahmoud Afshari

Etiology of congenital hypothyroidism in Isfahan: Does it different?

Volume 2014, January, January 2014, Pages 1-6

Mahin Hashemipour, Mahmoud Ghasemi, Silva Hovsepian, Kamal Heiydari, Ali Sajadi, Rezvaneh Hadian, Marjan Mansourian, Naghme Mirshahzadeh, Roya Kelishadi, Marzie Dalvi

Ultrasonographic evaluation of the thyroid gland volume among 8-15-year-old children in Isfahan, Iran

Volume 2014, January, January 2014, Pages 1-5

Maryam Moradi, Mahin Hashemipour, Shirin Akbari, Zahra Kor, Sayed Ali Mirbod, Mohammad Reza Kooshanmehr

Influence of perinatal factors on thyroid stimulating hormone level in cord blood

Volume 2013, June, June 2013, Pages 1-4

Amir-mohammad Armanian, Mahin Hashemipour, Azadeh Esnaashari, Roya Kelishadi, Ziba Farajzadegan

High prevalence of congenital hypothyroidism in Isfahan: Do familial components have a role?

Volume 2012, August, August 2012, Pages 1-5

Mahin Hashemipour, Silva Hovsepian, Roya Kelishadi

Advanced Biomedical Research