Advanced Biomedical Research
Author = Hashemipour, Mahin
Evaluation of growth hormone deficiency in children with cystic fibrosis
Volume 2022, july, July 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
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