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Gene Expression of TNF-α among Iraqi COVID-19 Patients with
a Different Severity Status
Siham Sahib Farhan , parisa tahmasebi, Hussein O. M. Al-Dahmoshi , Hayder Saeed Gatea
(2023)
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A novel pathogenic variant in the MARVELD2 gene causes autosomal
recessive non-syndromic hearing loss in an Iranian family
Afsaneh Taghipour-Sheshdeh , Fatemeh Nemati-Zargaran , Narges Zarepour , parisa tahmasebi, Nader Saki , Morteza Hashemzadeh-Chaleshtori , Javad Mohammadi-Asl , Mohammad Amin Tabatabaiefar
(2019)
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A Patient with Trisomy 4p and Monosomy 10q
Maryam Sobhani , parisa tahmasebi, Fatemeh Nasiri , Mitra Rahnama , Roxana Karimi-Nejad , Mohammad Amin Tabatabaiefar
(2019)
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Next-generation sequencing reveals a novel pathological mutation in the
TMC1 gene causing autosomal recessive non-syndromic hearing loss in an
Iranian kindred
Ladan Sadeghian , Mohammad Amin Tabatabaiefar , Najmeh Fattahi , Mohammad Reza Pourreza , parisa tahmasebi, Morteza Hashemzadeh Chaleshtori , Zahra Alavi
(2019)
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FREQUENCY OF GJB2 MUTATIONS IN FAMILIES WITH AUTOSOMAL RECESSIVE NON-SYNDROMIC HEARING LOSS IN KHUZESTAN PROVINCE
parisa tahmasebi, Morteza Hashemzadeh CHALESHTORI , Fatemeh ABDOLLAHNEJAD , Zahra ALAVI , Ladan SADEGHIAN , Mohammad Amin TABATABAIEFAR , Seyed Reza Kazemi NEZHAD , Nader SAKI , Javad MOHAMMADI-ASL , Farah TALEBI
(2018)
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A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss
Mohammad Amin Tabatabaiefar , Mohammad Reza Pourreza , parisa tahmasebi, Nader Saki , Morteza Hashemzadeh Chaleshtori , Javad Mohammadi-asl , Rasoul Salehi
(2018)
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A novel TECTA mutation causes ARNSHL
Samira Asgharzade , Mohammad Amin Tabatabaiefar , Mohammad Hossein Modarressi , Mohammad Hossein Ghahremani , Somayeh Reiisi , Morteza Hashemzadeh Chaleshtori , Fatemeh Abdollahnejad , parisa tahmasebi
(2016)
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