Works by Dehaghani, Elham Davoudi

Results: 14

Association of usf1s2 variant in the upstream stimulatory factor 1 gene with premature coronary artery disease in southern population of Iran.

Published in:

Tehran University Medical Journal, 2015, v. 72, n. 12, p. 838

By:

Jouyan, Najmeh;
Saffari, Babak;
Davoudi-Dehaghani, Elham;
Saliani, Negar;
Senemar, Sara;
Bahari, Marzieh;
Jouyan, Neda;
Mohammad Ali Ostovan

Publication type:

Article

GJB2 c.−23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.

Published in:

European Archives of Oto-Rhino-Laryngology, 2015, v. 272, n. 9, p. 2255, doi. 10.1007/s00405-014-3171-7

By:

Zeinali, Sirous;
Davoudi-Dehaghani, Elham;
Azadmehr, Sarah;
DabbaghBagheri, Samira;
Bagherian, Hamideh;
Jamali, Mojdeh;
Zafarghandimotlagh, Fatemeh;
Masoodifard, Mahboobeh;
BandehiSarhaddi, Ameneh;
Rejali, Leili;
Sahebi, Sepideh

Publication type:

Article

Identifying and predicting the pathogenic effects of a novel variant inducing severe early onset MMA: a bioinformatics approach.

Published in:

Hereditas, 2023, v. 160, n. 1, p. 1, doi. 10.1186/s41065-023-00281-0

By:

Maryami, Fereshteh;
Rismani, Elham;
Davoudi-Dehaghani, Elham;
Khalesi, Nasrin;
Motlagh, Fatemeh Zafarghandi;
Kordafshari, Alireza;
Talebi, Saeed;
Rahimi, Hamzeh;
Zeinali, Sirous

Publication type:

Article

SLC26A4 Pathogenic Variants as a Third Cause of Hearing Loss: Role of Three Exons in DFNB4 Deafness in Iran.

Published in:

Indian Journal of Otology, 2019, v. 25, n. 3, p. 146, doi. 10.4103/indianjotol.INDIANJOTOL_36_19

By:

Davoudi-Dehaghani, Elham;
Mahdieh, Nejat;
Shirkavand, Atefeh;
Bagherian, Hamideh;
DabbaghBagheri, Samira;
Zeinali, Sirous

Publication type:

Article

Identification and characterization of the largest deletion in the PCCA gene causing severe acute early-onset form of propionic acidemia.

Published in:

Molecular Genetics & Genomics, 2023, v. 298, n. 4, p. 905, doi. 10.1007/s00438-023-02023-3

By:

Maryami, Fereshteh;
Davoudi-Dehaghani, Elham;
Khalesi, Nasrin;
Rismani, Elham;
Rahimi, Hamzeh;
Talebi, Saeed;
Zeinali, Sirous

Publication type:

Article

The Most Common Types of 3.7 Kilobase Deletion in the Iranian Population.

Published in:

Hemoglobin, 2024, v. 48, n. 6, p. 365, doi. 10.1080/03630269.2024.2435379

By:

Askarian-Sardari, Fatemeh;
Esmaeilian, Samin;
Hajimohammadi, Zahra;
Hayat-Nosaeid, Mina;
Haghpour, Parisa;
Karimipoor, Morteza;
Davoudi-Dehaghani, Elham

Publication type:

Article

Development of a Quantitative Multiplex PCR to Detect Three Common Alpha Thalassemia Deletions.

Published in:

Hemoglobin, 2023, v. 47, n. 4, p. 163, doi. 10.1080/03630269.2023.2260744

By:

Hajimohammadi, Zahra;
Alimohammadi-Bidhendi, Sara;
Bagheri Amiri, Fahimeh;
Karimipoor, Morteza;
Davoudi-Dehaghani, Elham;
Entezam, Mona

Publication type:

Article

Regulatory Mutation Study in Cases with Unsolved Hypochromic Microcytic Anemia and α-Major Regulatory Element Haplotype Analysis in Iran.

Published in:

Hemoglobin, 2021, v. 45, n. 1, p. 37, doi. 10.1080/03630269.2021.1882482

By:

Alimohammadi-Bidhendi, Sara;
Azadmehr, Sarah;
Razipour, Masoumeh;
Zeinali, Sirous;
Eslami, Maryam;
Davoudi-Dehaghani, Elham

Publication type:

Article

Reporting the presence of three different diseases causing GJB2 mutations in a consanguineous deaf family.

Published in:

International Journal of Audiology, 2014, v. 53, n. 2, p. 128, doi. 10.3109/14992027.2013.850748

By:

Davoudi-Dehaghani, Elham;
Fallah, Mohammad-Sadegh;
Shirzad, Tina;
Tavakkoly-Bazzaz, Javad;
Bagherian, Hamideh;
Zeinali, Sirous

Publication type:

Article

Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencing.

Published in:

Acta Oto-Laryngologica, 2015, v. 135, n. 2, p. 125, doi. 10.3109/00016489.2014.969383

By:

Davoudi-Dehaghani, Elham;
Fallah, Mohammad-Sadegh;
Tavakkoly-Bazzaz, Javad;
Bagherian, Hamideh;
Zeinali, Sirous

Publication type:

Article

In silico Analysis of Two Novel Variants in the Pyruvate Carboxylase (PC) Gene Associated with the Severe Form of PC Deficiency.

Published in:

Iranian Biomedical Journal, 2023, v. 27, n. 5, p. 307, doi. 10.61186/ibj.27.5.307

By:

Maryami, Fereshteh;
Rismani, Elham;
Davoudi-Dehaghani, Elham;
Khalesi, Nasrin;
Talebi, Saeed;
Mahdian, Reza;
Zeinali, Sirous

Publication type:

Article

Once in a Blue Moon, a Very Rare Coexistence of Glutaric Acidemia Type I and Mucopolysaccharidosis Type IIIB in a Patient.

Published in:

2020

By:

Alaei, Mohammad Reza;
Kheirkhahan, Meghdad;
Talebi, Saeed;
Davoudi-Dehaghani, Elham;
Keramatipour, Mohammad

Publication type:

journal article

The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia A.

Published in:

Archives of Iranian Medicine (AIM), 2021, v. 24, n. 12, p. 887, doi. 10.34172/aim.2021.133

By:

Azadmehr, Sarah;
Rahiminejad, Faezeh;
Motlagh, Fatemeh Zafarghandi;
Jamali, Mojdeh;
Tehrani, Pardis Ghazizadeh;
Shirzadeh, Tina;
Bagherian, Hamideh;
Karimipoor, Morteza;
Davoudi-Dehaghani, Elham;
Zeinali, Sirous

Publication type:

Article

Sex chromosome aneuploidy in cytogenetic findings of referral patients from south of Iran.

Published in:

Iranian Journal of Reproductive Medicine, 2012, v. 10, n. 2, p. 141

By:

Jouyan, Najmeh;
Dehaghani, Elham Davoudi;
Senemar, Sara;
Shojaee, Ashraf;
Mozdarani, Hossein

Publication type:

Article