Zobrazeno 1 - 10
of 150
pro vyhledávání: '"Morteza HASHEMZADEH CHALESHTORI"'
Autor:
Ameneh Mehri-Ghahfarrokhi, Zahra Pourteymourfard-Tabrizi, Effat Farrokhi, Morteza Hashemzadeh Chaleshtori, Mohammad-Saeid Jami
Publikováno v:
Journal of Otology, Vol 14, Iss 4, Pp 121-127 (2019)
Auditory neuropathy is the particular form of deafness in humans which cannot be treated by replacement therapy. Human dental pulp stem cells (hDPSCs) are derived from an ectomesenchymal neural crest cell population. Therefore, they possess a promisi
Externí odkaz:
https://doaj.org/article/9338a30b2e7d43529075bb629c470c53
Autor:
Mahtab Khosrofar, Mohammad Reza Pourreza, Samira Asgharzadeh, Parisa Tahmasebi, Elahe Ali Asgari, Reza Ghasemikhah, Nader Saki, Javad Mohammadi-asl, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar
Publikováno v:
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, Vol 20, Iss 3, Pp 31-38 (2017)
Abstract Background: Hearing loss (HL) is the most common congenital defect in humans. One or two in thousand newborn babies have prelingual hearing loss. Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common form of hereditary
Externí odkaz:
https://doaj.org/article/0b6436825bd847978cc57b11e4bf8bbf
Autor:
Somayeh Reiisi, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori
Publikováno v:
Iranian Journal of Basic Medical Sciences, Vol 19, Iss 7, Pp 772-778 (2016)
Objective(s): Non-syndromic sensorineural hearing loss (NSHL) is a common disorder affecting approximately 1 in 500 newborns. This type of hearing loss is extremely heterogeneous and includes over 100 loci. Mutations in the GJB2 gene have been implic
Externí odkaz:
https://doaj.org/article/ac64cd331f44480db0c7d94a0a1a9c8f
Autor:
Akram Sarmadi, Aliasgar Mohammadi, Fatemeh Tabatabaei, Zahra Nouri, Morteza Hashemzadeh Chaleshtori, Mohammad Amin Tabatabaiefar
Publikováno v:
Advanced Biomedical Research, Vol 9, Iss 1, Pp 25-25 (2020)
Background: Diabetes mellitus (DM) is a group of metabolic disorders in the body, accompanied with increasing blood sugar levels. Diabetes is classified into three groups: Type 1 DM (T1DM), Type 2 DM (T2DM), and monogenic diabetes. Maturity-onset dia
Externí odkaz:
https://doaj.org/article/a85b13760df5402db45ec18f016876aa
Autor:
Raziyeh KARAMI ESHKAFTAKI, Effat FARROKHI, Fatemeh HEYBATI GOJANI, Najmeh SALEHI VANANI, Maryam KARAMI ESHKAFTAKI, Ezzatollah MEMARZADEH, Morteza HASHEMZADEH CHALESHTORI
Publikováno v:
Iranian Journal of Public Health, Vol 47, Iss 3 (2018)
No Abstract###
Externí odkaz:
https://doaj.org/article/5b57ead7ec9843a283caa4a666470e5d
Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients
Autor:
Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori, Shahrbanoo Parchami, Abbas Doosti
Publikováno v:
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, Vol 18, Iss 5, Pp 59-67 (2015)
Abstract Background: Hypertrophic cardiomyopathy (HCM) is a various collection of heart diseases with autosomal dominant inheritance affecting 0.2% of the global population. HCM is also the most common cause of sudden cardiac death in individuals yo
Externí odkaz:
https://doaj.org/article/9466cd1c474f431ca250160de0bd8059
Autor:
Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI
Publikováno v:
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://doaj.org/article/0f3b73e0bdae46558d55f882a79be9ad
Autor:
Somayeh Reiisi, Mohammad Hossein Sanati, Mohammad Amin Tabatabaiefar, Hamid Reza Pourjafari, Zarrin Minuchehr, Afsaneh Shavarzi, Mitra Ataie, Mahbobeh Kasiri, Morteza Hashemzadeh Chaleshtori
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 32, Iss 285, Pp 669-677 (2014)
مقدمه: ناشنوایی یک اختلال شایع میباشد که به طور معمول، هتروژنی ژنتیکی را در جمعیتهای انسانی نشان میدهد. بروز ناشنوایی مادرزادی به می
Externí odkaz:
https://doaj.org/article/00ed8153290b4311803aa86522ae56e6
Autor:
Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj
Publikováno v:
Cell Journal, Vol 16, Iss 2, Pp 225-230 (2014)
Uterine leiomyoma (UL) is the most common benign smooth muscle cell tumor with as yet unknown etiology and pathogenesis. This study was carried out to investigate the association of ESR1-351 A>G, ESR1 -397 T>C and CYP1A1 (Ile462Val) polymorphisms wit
Externí odkaz:
https://doaj.org/article/b72c16d2d1c744418d736ff9104a2117
Publikováno v:
Journal of Kerman University of Medical Sciences, Vol 21, Iss 6, Pp 540-550 (2014)
Background & Aims: SLC26A4 gene mutations are the second identifiable genetic cause of autosomal recessive nonsyndromic hearing loss (ARNSHL) after GJB2 mutations and are currently investigated in molecular diagnosis.In databases, several potential S
Externí odkaz:
https://doaj.org/article/c61bef025f84430e9ca7ffa2f5a1e476