Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Najmeh Fattahi"'
Autor:
Azam Pourahmadiyan, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Paria Alipour, Najmeh Fattahi, Morteza Hashemzadeh-Chaleshtori
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 34, Iss 374, Pp 214-220 (2016)
مقدمه: ناشنوایی حسی- عصبی، رایج‌ترین ناهنجاری عصبی است که با میانگین 1 در 1000-500 نوزاد رخ می‌دهد. موارد غیر سندرمی، 70 درصد ناشنوایی‌ها را ش
Externí odkaz:
https://doaj.org/article/1b611da6347a4163a911526fb8086538
Autor:
Parya Alipour, Mohammad Amin Tabatabaiefar, Somayeh Reiisi, Najmeh Fattahi, Azam Pourahmadian, Mortaza Hashemzadeh-Chaleshtori
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 33, Iss 346, Pp 1308-1317 (2015)
مقدمه: ناشنوایی یک اختلال حسی- عصبی است و یکی از شایع‌ترین نقص‌های مادرزادی می‌باشد که دارای بروز یک در هزار در بین نوزادان می‌باشد. مطا
Externí odkaz:
https://doaj.org/article/a351f2cce6904b89bdee2dbe434ef791
It is found that the death of retinal photoreceptors is the main cause of retinal degeneration, while there is not an effective treatment protocol. Data of preclinical and clinical trials indicates that the stem cell therapy is a useful way of treati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b8bac80dd6028b72a13a9153aa488aa
https://doi.org/10.21203/rs.3.rs-748878/v1
https://doi.org/10.21203/rs.3.rs-748878/v1
Autor:
Paria Alipour, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar, Fateme Rezaeian, Azam Pourahmadiyan, Mahbubeh Kasiri, Najmeh Fattahi, Javad Mohammadi-Asl, Afsaneh Taghipour-Sheshdeh
Publikováno v:
International Journal of Audiology. 58:628-634
Objective: Hearing loss (HL) is a common sensory deficit with high phenotypic and genotypic heterogeneity. A large Iranian family with HL was genetically assessed in this study.Design: A pr...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8c052180abf83760d02bc74b034f6305
https://doi.org/10.1080/14992027.2019.1619945
https://doi.org/10.1080/14992027.2019.1619945
Autor:
Mohammad Amin Tabatabaiefar, Mohammad Reza Pourreza, Najmeh Fattahi, Javad Tavakkoly Bazzaz, Reza Sharifi, Shahnaz Zarifi, Mojtaba Darbouy, Azam Ahmadi Shadmehri, Mahboobeh Koohiyan
Publikováno v:
Journal of Cellular Biochemistry. 120:3367-3372
Glutaric acidemia type I (GA-1) is an inborn error of metabolism due to deficiency of glutaryl-CoA dehydrogenase (GCDH), which catalyzes the conversion of glutaryl-CoA to crotonyl-CoA. GA-1 occurs in about 1 in 100 000 infants worldwide. The GCDH gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d82ab2406f8638633ecc55fea25d8a8d
https://doi.org/10.1002/jcb.27607
https://doi.org/10.1002/jcb.27607
Autor:
Azam, Pourahmadiyan, Paria, Alipour, Najmeh, Fattahi, Mahbubeh, Kasiri, Fateme, Rezaeian, Afsaneh, Taghipour-Sheshdeh, Javad, Mohammadi-Asl, Mohammad Amin, Tabatabaiefar, Morteza, Hashemzadeh Chaleshtori
Publikováno v:
International journal of audiology. 58(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7de073a877dc5b8da56d61d2a0331574
https://pubmed.ncbi.nlm.nih.gov/31187663
https://pubmed.ncbi.nlm.nih.gov/31187663
Autor:
Mohammad Reza Pourreza, Najmeh Fattahi, Zahra Alavi, Parisa Tahmasebi, Morteza Hashemzadeh Chaleshtori, Ladan Sadeghian, Mohammad Amin Tabatabaiefar
Publikováno v:
International journal of pediatric otorhinolaryngology. 124
Objectives Hearing loss (HL) is the most common sensory-neural disorder with excessive clinical and genetic heterogeneity, which negatively affects life quality. Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common form of the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7e011e1cdabfab2ab44d933c20b5c57
https://pubmed.ncbi.nlm.nih.gov/31176026
https://pubmed.ncbi.nlm.nih.gov/31176026
Autor:
Neda Golchin, Javad Mohammadi-Asl, Laleh Shariati, Najmeh. Fattahi, Paria Alipour, Mohammad Amin Tabatabaiefar, Azam Pourahmadiyan
Publikováno v:
Journal of the neurological sciences. 379
Ataxia telangiectasia (A-T) is a neurodegenerative autosomal recessive disorder with the main characteristics of progressive cerebellar degeneration, sensitivity to ionizing radiation, immunodeficiency, telangiectasia, premature aging, recurrent sino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f04ae4cf8b2de230d1a6c74b34850950
https://pubmed.ncbi.nlm.nih.gov/28716242
https://pubmed.ncbi.nlm.nih.gov/28716242