Maryam Taghdiri

发表

Cardiovascular, lactate and appetite response to light and spicy music tempo after an endurance swimming protocol in young girls

J. Mehrabani, A. Jorbonian, S. Bagherzadeh, 2020 .

Concomitant Increase of OX40 and FOXP3 transcripts in peripheral blood of patients with breast cancer.

A. Talaiezadeh, A. Khodadadi, G. Solgi, 2013, Iranian journal of immunology : IJI.

Safety and Efficacy of Combined Intramuscular/Intranasal RAZI-COV PARS Vaccine Candidate Against SARS-CoV-2: A Preclinical Study in Several Animal Models

A. Es‐haghi, Z. Hassan, M. Hajimoradi, 2022, Frontiers in Immunology.

Reporting one very rare pathogenic variation c.1106G>A in POMT2 gene.

M. Faghihi, Maryam Taghdiri, G. Mahjoub, 2020, Intractable & rare diseases research.

Identification of SLC26A4 gene mutations in Iranian families with hereditary hearing impairment

K. Kahrizi, H. Najmabadi, C. Nishimura, 2009, European Journal of Pediatrics.

Advanced molecular approaches pave the road to a clear-cut diagnosis of hereditary retinal dystrophies

V. Yassaee, M. Miryounesi, M. Fardaei, 2018, Molecular vision.

Genetics of intellectual disability in consanguineous families

T. Wienker, Wei Chen, R. Herwig, 2019, Molecular Psychiatry.

Finding mutation within non-coding region of GJB2 reveals its importance in genetic testing of hearing loss in Iranian population.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2015, International journal of pediatric otorhinolaryngology.

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

Allen C. Simpson, M. Farhadi, K. Kahrizi, 2015, Journal of Medical Genetics.

The novel mutation in the COL7A1 gene in the patient with dystrophic forms of epidermolysis bullosa

M. Fardaei, Maryam Taghdiri, Seyed Mohammad Bagher Tabei, 2020 .

The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.

K. Kahrizi, H. Najmabadi, F. Mojahedi, 2012, International journal of pediatric otorhinolaryngology.

A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome

M. Faghihi, M. Fardaei, H. Dastsooz, 2017, Front. Pediatr..

Two Novel Mutations in LAMC2 Gene in Iranian Families Affected by Junctional Epidermolysis Bullosa.

M. Fardaei, S. Tabei, Maryam Taghdiri, 2022, Reports of biochemistry & molecular biology.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.

Identification of a novel deletion within ALDH3A2 gene in an Iranian Family with Sjögren–Larsson Syndrome

M. Miryounesi, M. Fardaei, Maryam Taghdiri, 2017, Clinical case reports.

Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran

Allen C. Simpson, M. Farhadi, K. Kahrizi, 2015, Journal of Medical Genetics.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.