Investigating the relationship of genetic mutations in GJB2 and linkage analysis of DFNB4 Locus in a group of non-syndromic hearing impaired people with autosomal recessive inherit...

by Najmeh Ahangari, Marjan Masoudi, Aliakbar Poursadegh, Abdolazim Nejatizadeh
Published 2014-12-01

Misdiagnosed Aicardi Goutières Syndrome Patient: A Case Report

by Mohammad Moein Vakilzadeh, Najmeh Ahangari, Ehsan Ghayoor Karimiani, Mehran Beiraghi Toosi
Published 2021-10-01

Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss

by Marjan MASOUDI, Najmeh AHANGARI, Ali Akbar POURSADEGH ZONOUZI, Ahmad POURSADEGH ZONOUZI, Azim NEJATIZADEH
Published 2016-05-01

A Novel Heterozygous ACAN Variant in an Iranian Family with Short Stature: A Case Report

by Amirsaeed Aghabozorgi, Najmeh Ahangari, Moein Mobini, Rahim Vakili, Mohammad Doosti, Saba Vakili, Ehsan Karimiani
Published 2022-09-01

Limb-girdle muscular dystrophy type 2B (LGMD2B) caused by pathogenic splice and missense variants of DYSF gene among Iranians with muscular dystrophy

by Fatemeh Arab, Najmeh Ahangari, Hadis Malek, Mohammad Doosti, Paria Najarzadeh Torbati, Ehsan Ghayoor Karimiani
Published 2023-01-01

The effect of nanomicelle curcumin, sorafenib, and combination of the two on the cyclin D1 gene expression of the hepatocellular carcinoma cell line (HUH7)

by sareh Hosseini, jamshidkhan chamani, Mohadeseh Sinichi, Amir Mohammad Bonakdar, Zeinolabedin Azad, Najmeh Ahangari, Hamid Reza Rahimi
Published 2019-10-01

Genetic Linkage Analysis of DFNB4, DFNB28, DFNB93 Loci in Autosomal Recessive Non-syndromic Hearing Loss: Evidence for Digenic Inheritance in GJB2 and GJB3 Mutations

by Marzieh NASERI, Masoud AKBARZADEHLALEH, Marjan MASOUDI, Najmeh AHANGARI, Ali Akbar POURSADEGH ZONOUZI, Ahmad POURSADEGH ZONOUZI, Leila SHAMS, Azim NEJATIZADEH
Published 2017-12-01

Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndrom...

by Masoud Akbarzadeh Laleh, Marzieh Naseri, Ali Akbar Poursadegh Zonouzi, Ahmad Poursadegh Zonouzi, Marjan Masoudi, Najmeh Ahangari, Leila Shams, Azim Nejatizadeh
Published 2017-01-01

Unbalanced segregation of a paternal t(9;11)(p24.3;p15.4) translocation causing familial Beckwith-Wiedemann syndrome: a case report

by Caroline Lekszas, Indrajit Nanda, Barbara Vona, Julia Böck, Farah Ashrafzadeh, Nahid Donyadideh, Farnoosh Ebrahimzadeh, Najmeh Ahangari, Reza Maroofian, Ehsan Ghayoor Karimiani, Thomas Haaf
Published 2019-06-01

ECEL1 novel mutation in arthrogryposis type 5D: A molecular dynamic simulation study

by Najmeh Ahangari, Nazanin Gholampour‐Faroji, Mohammad Doosti, Majid Ghayour Mobarhan, Sima Shahrokhzadeh, Ehsan Ghayoor Karimiani, Bahareh Hasani‐sabzevar, Paria Najarzadeh Torbati, Aliakbar Haddad‐Mashadrizeh
Published 2023-06-01

Expanding the clinical phenotype of IARS2-related mitochondrial disease

by Barbara Vona, Reza Maroofian, Emanuele Bellacchio, Maryam Najafi, Kyle Thompson, Ahmad Alahmad, Langping He, Najmeh Ahangari, Abolfazl Rad, Sima Shahrokhzadeh, Paulina Bahena, Falk Mittag, Frank Traub, Jebrail Movaffagh, Nafise Amiri, Mohammad Doosti, Reza Boostani, Ebrahim Shirzadeh, Thomas Haaf, Daria Diodato, Miriam Schmidts, Robert W. Taylor, Ehsan Ghayoor Karimiani
Published 2018-11-01