Zobrazeno 1 - 10
of 31
pro vyhledávání: '"M Montazer zohour"'
Autor:
MA Tabatabaiefar, F Alasti, M Montazer Zohour, L Shariati, E Farrokhi, DD Farhud, GV Camp, MR Noori-Daloii, M Hashemzadeh Chaleshtori
Publikováno v:
Iranian Journal of Public Health, Vol 40, Iss 2, Pp 34-38 (2011)
"nBackground: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been id
Externí odkaz:
https://doaj.org/article/308cfe61f6db4851b9e011e0f8c6f5ee
Autor:
M Hashemzadeh Chaleshtori, M Montazer Zohour, L Hoghooghi Rad, H Pour-Jafari, DD Farhud, M Dolati, K Safa Chaleshtori, R Sasanfar, A Hosseinipour, L Andonian, A Tolouei, M Ghadami, MA Patton
Publikováno v:
Iranian Journal of Public Health, Vol 35, Iss 1, Pp 88-91 (2006)
Despite the enormous heterogeneity of genetic hearing loss, mutations in the GJB2 (connexin 26) gene located on “DFNB1” locus (13q12) account for up to 50% of cases of autosomal recessive non-syndromic hearing loss (ARNSHL) in some populations. T
Externí odkaz:
https://doaj.org/article/94624327e9134bf5967b9c2cfabddedc
Autor:
M Hashemzadeh Chaleshtori, L Hoghooghi Rad, M Dolati, R Sasanfar, A Hoseinipour, M Montazer Zohour, H Pourjafari, A Tolooi, M Ghadami, DD Farhud, MA Patton
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 1-7 (2005)
While hearing loss has been considered to be a very heterogeneous disorder, mutations in Gap junction beta 2 (GJB2) gene encoding Connexin 26 (Cx26) protein are the major cause of autosomal recessive and sporadic non-syndromic deafness in many popula
Externí odkaz:
https://doaj.org/article/5e3612f03f464d559a75c18adfbc9247
Autor:
A Hosseinipour, M Hashemzadeh Chaleshtori, R Sasanfar, DD Farhud, A Tolooi, M Doulati, L Hoghooghi Rad, M Montazer zohour, M Ghadami
Publikováno v:
Iranian Journal of Public Health, Vol 34, Iss 1, Pp 47-50 (2005)
Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this
Externí odkaz:
https://doaj.org/article/b7821cb7395c4601940b4fc2ffa18cf5
Autor:
R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori
Publikováno v:
Iranian Journal of Public Health, Vol 33, Iss 4, Pp 26-30 (2004)
The 35delG mutation in the Connexin 26 gene (Cx26), at the DNFB1 locus is the most common mutation in the patients with autosomal recessive non-syndromic hearing loss (ARNSHL). We have studied a total of 224 deaf cases from 189 families in two popula
Externí odkaz:
https://doaj.org/article/90399c1b2ce0486eaf2c4a732eeca568
Autor:
M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton "
Publikováno v:
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste
Externí odkaz:
https://doaj.org/article/a458d4a14e3543a18e8b538ea71f31ec
Autor:
M. Montazer Zohour
Publikováno v:
Indian Journal of Science and Technology. 5:1-6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9293b88107e67a2961e766b7f3c21c59
https://doi.org/10.17485/ijst/2012/v5i10.4
https://doi.org/10.17485/ijst/2012/v5i10.4
Autor:
Ma, Tabatabaiefar, F, Alasti, M Montazer, Zohour, L, Shariati, E, Farrokhi, Dd, Farhud, Gv, Camp, Mr, Noori-Daloii, M Hashemzadeh, Chaleshtori
Publikováno v:
Iranian Journal of Public Health
Background: Hearing loss (HL) is the most frequent sensory birth defect in humans. Autosomal recessive non-syndromic HL (ARNSHL) is the most common type of hereditary HL. It is extremely heterogeneous and over 70 loci (known as DFNB) have been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::00f47b81ce928e93f9313a733f80a9d1
https://pubmed.ncbi.nlm.nih.gov/23113071
https://pubmed.ncbi.nlm.nih.gov/23113071
Autor:
'M Hashemzadeh Chaleshtori, M Dowlati, DD Farhud, L Hoghooghi Rad, R Sasanfar A Hoseinipour, M Montazer Zohour, A Tolooi, M Ghadami, HR Pourjafari, MA Oshaghi, MA Patton \\'
Publikováno v:
Iranian Journal of Public Health, Vol 33, Iss 2 (2004)
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Iranian Journal of Public Health, Vol 33, Iss 2, Pp 14-19 (2004)
Mutations in the GJB2 gene encoding Connexin 26 (Cx26) protein are a major cause for autosomal recessive non syndromic and sporadic deafness in many populations. In this study we have investigated the prevalence of the GJB2 gene mutations using neste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::071856730eb048591ef9426273e79951
https://ijph.tums.ac.ir/index.php/ijph/article/view/1910
https://ijph.tums.ac.ir/index.php/ijph/article/view/1910
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