Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Marzieh Mohseni"'
Autor:
Fereshteh Jamshidi, Ebrahim Shokouhian, Marzieh Mohseni, Kimia Kahrizi, Hossein Najmabadi, Mojgan Babanejad
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Background To date, over 400 syndromes with hearing impairment have been identified which altogether constitute almost 30% of hereditary hearing loss (HL) cases around the globe. Manifested as complete or partial labyrinthine aplasia (severe
Externí odkaz:
https://doaj.org/article/39d97996c2e04ea79d5a364f6c386c99
Publikováno v:
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum, Vol 15, Iss 11, Pp 724-733 (2022)
Background and Objectives: The increasing demand of people and students for computer technology and the Internet has caused mental health problems and social communication in them. In this study, the relationship between Internet addiction and genera
Externí odkaz:
https://doaj.org/article/4c02f2264e4843f8a299e4a6c644bee0
Publikováno v:
Kidney & Blood Pressure Research, Vol 43, Iss 2, Pp 471-478 (2018)
Background/Aims: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common inherited cystic kidney diseases caused by mutations in two large multi-exon genes, PKD1 and PKD2. High allelic heterogeneity and duplication of PKD1 exon
Externí odkaz:
https://doaj.org/article/70d27d01833f458bbe4a79302d03f949
Publikováno v:
Iranian Rehabilitation Journal, Vol 15, Iss 2, Pp 149-154 (2017)
Objectives: Polymorphisms in α-actinin-3 (ACTN3) gene are considered to be important in the genetic predisposition to human athletic performance. Most of the activities in soccer such as jumping, striking the ball, and running are considered plyomet
Externí odkaz:
https://doaj.org/article/91857d6dff8a499c8e85c529703fbf70
Autor:
Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi, Michael Nothnagel
Publikováno v:
PLoS Genetics, Vol 15, Iss 9, p e1008385 (2019)
Iran, despite its size, geographic location and past cultural influence, has largely been a blind spot for human population genetic studies. With only sparse genetic information on the Iranian population available, we pursued its genome-wide and geog
Externí odkaz:
https://doaj.org/article/4315684f000740c9942734ccd2e1d473
Autor:
Elaheh Papari, Akram Farhadi, Ma'soumeh Hosseini, Seyyedeh Sedigheh A'bedini, Marzieh Mohseni, Sousan Bani-Hashemi, Sanaz Arjangi, Farkhndeh Behjati, Kimia Kahrizi, Hossein Najm-Abadi
Publikováno v:
Journal of Rehabilitation, Vol 13, Iss 4, Pp 58-64 (2013)
Objective: About 50% of severe to profound intellectual disabilities (ID) are caused by genetic factors. In this study we decided to investigate the genetic causes of ID in 69 Bushehrian families to provide information for genetic counseling, carrier
Externí odkaz:
https://doaj.org/article/3f3c2499c4e54105998fbbc015e82d82
Autor:
Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi
Publikováno v:
Journal of Rehabilitation, Vol 8, Iss 3, Pp 35-41 (2007)
Objective: Hereditary hearing loss (HHL) is a very common disorder. When inherited in an autosomal recessive manner, it typically presents as an isolated finding. Interestingly and unexpectedly, in spite of extreme heterogeneity, mutations in one gen
Externí odkaz:
https://doaj.org/article/e891523139e44bb594ba117ed736dacc
Autor:
Parisa Imani-Raad, Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Golnaz As'adi, Noushin Nik-Zaat, Fatemeh Sadat Esteghamat, Hossein Najm-Abadi
Publikováno v:
Journal of Rehabilitation, Vol 7, Iss 1, Pp 49-52 (2006)
Objective: Congenital hearing loss occurs in 1 out of 1000 births and about 50% of all cases are estimated to be of genetic origin. About 70% of hereditary hearing loss is non-syndromic with autosomal recessive inheritance accounting for 80% of the g
Externí odkaz:
https://doaj.org/article/301d86ac0cf64cc098907ddc1dd1cc44
Autor:
Yousef Shafeghati, Ahmad Ebrahimi, Marzieh Mohseni, Farzaneh Ostadi, Halleh Habibi, Hamid Poujafari, R.J.H Esmith, Hosein Najmabadi
Publikováno v:
پزشکی بالینی ابن سینا, Vol 12, Iss 4, Pp 23-27 (2006)
Introduction & Objective : Hearing loss is the most prevalent form of sensory impairment in humans, affecting approximately one in 1000 infants. In more than half of the cases, the deafness is inherited, and about 80% of hereditary deafness transmitt
Externí odkaz:
https://doaj.org/article/f70e5b7f7d48450c8c488bf5b5272142
Autor:
Hossein Najm-Abadi, Kimia Kahrizi, Marzieh Mohseni, Fatemeh Sadat Esteghamat, Sanaz Arzhangi, Richard Smith
Publikováno v:
Journal of Rehabilitation, Vol 5, Iss 4, Pp 58-61 (2005)
The incidence of profound congenital hearing loss is about 1 in 1,000 live birth. There are more than 50 distinct genetic loci (known as DFNB loci) at which mutations can cause recessive hearing loss. DFNB4, one recessive locus for deafness, also map
Externí odkaz:
https://doaj.org/article/b521439ef6294da8978b60617bef3d34