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Papers published by Ms Maryam Balali:
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
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
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
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
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