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Papers published by Ms Maryam Balali:
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Association of genetic variations in the mitochondrial DNA control region with presbycusis
Falah M, Farhadi M, Kamrava SK, Mahmoudian S, Daneshi A, Balali M, Asghari A, Houshmand M
Clinical Interventions in Aging 2017, 12:459-465
Published Date: 3 March 2017
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Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
![](cr_data/cache/submission_images/s111000/111717/27_sep_2016_figure_3_200_200_90.jpg)
Akbaroghli S, Balali M, Kamalidehghan B, Saber S, Aryani O, Yong Meng G, Houshmand M
Therapeutics and Clinical Risk Management 2017, 13:15-19
Published Date: 20 December 2016
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The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusis
Falah M, Houshmand M, Najafi M, Balali M, Mahmoudian S, Asghari A, Emamdjomeh H, Farhadi M
Therapeutics and Clinical Risk Management 2016, 12:1573-1578
Published Date: 19 October 2016
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Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss
Balali M, Kamalidehghan B, Farhadi M, Ahmadipour F, Ashkezari MD, Hemami MR, Arabzadeh H, Falah M, Meng GY, Houshmand M
Therapeutics and Clinical Risk Management 2016, 12:117-128
Published Date: 28 January 2016