Zobrazeno 1 - 10
of 185
pro vyhledávání: '"Hashemzadeh-Chaleshtori M"'
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 16, Iss 2, Pp 82-88 (2014)
Background and Objective: SLC26A4 gene mutations after GJB2 mutations are the second currently identifiable genetic cause of autosomal recessive non syndromic hearing loss (ARNSHL) which currently is used in molecular diagnosis of ARNSHL. Several pot
Externí odkaz:
https://doaj.org/article/262125ffcb5542a4bd4b3d0987cb294c
Publikováno v:
Breast Cancer: Targets and Therapy, Vol Volume 11, Pp 293-301 (2019)
Maryam Motamedi,1 Morteza Hashemzadeh Chaleshtori,1 Sorayya Ghasemi,1 Fariborz Mokarian2 1Cellular and Molecular Research Center, Basic Health Sciences Institute, Shahrekord University of Medical Sciences, Shahrekord, Iran; 2Department of Hematology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::e8a6d08cb66ff709d64b3a2b8fe9e891
https://www.dovepress.com/plasma-level-of-mir-21-and-mir-451-in-primary-and-recurrent-breast-can-peer-reviewed-article-BCTT
https://www.dovepress.com/plasma-level-of-mir-21-and-mir-451-in-primary-and-recurrent-breast-can-peer-reviewed-article-BCTT
Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 19, Iss 3, Pp 76-84 (2017)
Background and aims: Hearing loss (HL) is a most common sensory deficit in humans and approximately one in 1,000 newborns has severe-to-profound HL. About 50% of HL cases are inherited and approximately 70 percent of HL cases are Non-syndromic that a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::3a8eb301cd8f3f6f7439dbd5272fb95c
https://doaj.org/article/6e34be27c9e84820b387a633f95c56ec
https://doaj.org/article/6e34be27c9e84820b387a633f95c56ec
Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 18, Iss 6, Pp 6-17 (2017)
Background and aims: Hearing loss, a sensorineural disorder, is one of the most common congenital impairments, occurring in approximately 1 in 500 newborns. Hearing loss is a highly heterogenic disease and half of the cases of deafness are attributed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::50bbf0e99407b0856bdaa8e7d6b102dc
https://doaj.org/article/97f1469804a340b6ab0df065c9513630
https://doaj.org/article/97f1469804a340b6ab0df065c9513630
Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 19, Iss 2, Pp 124-132 (2017)
Background and aims: Hearing loss (HL) is the most common sensorineural disorder affecting 1 in 1000 newborns. About 70% of genetic HL is classified as nonsyndromic deafness. Over 100 non-syndromic loci have been identified in autosomal recessive non
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f20f470c15c2781daadad0ca8a934d39
https://doaj.org/article/53129f5648194968bfac7d52e1482c4f
https://doaj.org/article/53129f5648194968bfac7d52e1482c4f
Autor:
Nemati-Zargaran F, Tabatabaiefar MA, Taghipour-Sheshdeh A, Moradi F, Zarepour N, Hashemzadeh-Chaleshtori M
Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 19, Iss 1, Pp 1-9 (2017)
Background and aims: Hearing loss is a common sensorial disorder. There are approximately 360 million affected people all over the world. More than 50% of hearing loss is because of genetics factors. About 70% of inherited hearing loss is due to non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::f5682f7bb17ec893d5237b394a69681e
https://doaj.org/article/6d90a106f28449f5a15d5d7c9d9ce46b
https://doaj.org/article/6d90a106f28449f5a15d5d7c9d9ce46b
Publikováno v:
Iranian Journal of Public Health
Scopus-Elsevier
Iranian Journal of Public Health, Vol 46, Iss 1 (2017)
Scopus-Elsevier
Iranian Journal of Public Health, Vol 46, Iss 1 (2017)
Background: Hearing loss (HL) is the most frequent neurosensory impairment. HL is highly heterogeneous defect. This disorder affects 1 out of 500 newborns. This study aimed to determine the role of DFNB2 locus and frequency of MYO7A gene mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::8bdba5365c7988fed79efafb50c3fd87
http://europepmc.org/articles/PMC5401939
http://europepmc.org/articles/PMC5401939
Akademický článek
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Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 18, Iss 4, Pp 1-8 (2016)
Background and aims: Keratoconus (KC) is a degenerative eye disorder, which is leading to irregular corneal surface, thinning of cornea, changing the shape of a cone and decreased vision. The disease incidence between 1/500 to 1/2,000 people worldwid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::666a7e2c0f9cd828171da6076cfef886
https://doaj.org/article/cda0fbcfbe614162a3e7df4fbcc9bc9d
https://doaj.org/article/cda0fbcfbe614162a3e7df4fbcc9bc9d
Publikováno v:
Journal of Shahrekord University of Medical Sciences, Vol 18, Iss 3, Pp 8-18 (2016)
Background and aims: Hearing loss is a most common sensory deficit in humans. The hearing loss may be conductive, sensorineural, or mixed (syndromic or nonsyndromic), prelingual or postlingual. Due to the complexity of the hearing mechanism, it is no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::82a8cc6193bce6b76b815d04576046d4
https://doaj.org/article/1cd5f312060d4020b1f5dbde02a01d8d
https://doaj.org/article/1cd5f312060d4020b1f5dbde02a01d8d