Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rezvaneh Hadian"'
Autor:
Mahin Hashemipour, Mahmoud Ghasemi, Silva Hovsepian, Kamal Heiydari, Ali Sajadi, Rezvaneh Hadian, Marjan Mansourian, Naghme Mirshahzadeh, Marzie Dalvi
Publikováno v:
International Journal of Preventive Medicine, Vol 4, Iss 12, Pp 1365-1370 (2013)
Background: Considering the importance to determine the reasons for the higher occurrence of congenital hypothyroidism (CH) in Iran, in this study we report the prevalence of permanent CH (PCH) in Isfahan province 7 years after initiation of CH scree
Externí odkaz:
https://doaj.org/article/f8207fd4f4bd4586ae0002a66166cc74
Autor:
Kamal Heidari, Sayyed Ali Sajjadi, Rezvaneh Hadian, Somayeh Hadi, Ramesh Hosseinkhani, Soudabeh Amini, Zahra Kiani, Ali Ajami, Reza Fadaei, Anahita Shahriari, Kasra Keramatian
Publikováno v:
International Journal of Preventive Medicine, Vol 3, Iss 3, Pp 173-180 (2012)
Background: This study aimed to establish a comprehensive screening and referral system for chronic non-communicable diseases (CNCD) in the routine primary health care, and to determine the prevalence of diabetes, pre-diabetes, metabolic syndrome, an
Externí odkaz:
https://doaj.org/article/17e1b8961b794aba94d88e4c5ab24d82
Autor:
Nasibeh Hasani, Bahar Dehghan, Masood Amini, Kamal Heidari, Ali Sajadi, Ali Ajami, Masoomeh Dastanpour, Rezvaneh Hadian, Ashraf Aminoroaya, Zahra Pournaghshband, Silva Hovsepian, Mahin Hashemipour
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 27, Iss 94, Pp 135-142 (2009)
Background: Congenital hypothyroidism (CH) is a relatively common congenital disorder in neonates. Recently, a considerable proportion of familial cases have been identified, and possible roles of autoimmune factors suggested. The aim of this study w
Externí odkaz:
https://doaj.org/article/2eb1e3a8233d45cb988c796e4ae6d060
Autor:
Mahin Hashemipour, Fahimeh Soheilipour, Sakineh Karimizare, Hossein Khanahmad, Morteza Karimipour, Sepideh Aminzadeh, Leila Kokabee, Massoud Amini, Silva Hovsepian, Rezvaneh Hadian
Publikováno v:
International Journal of Endocrinology, Vol 2012 (2012)
Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormon
Externí odkaz:
https://doaj.org/article/d528decbb8514d4c864c49b97ad88d2f
Autor:
Mehdi Salek, Mahin Hashemipour, Mostafa Hashemi, Mahsa Hajrahimi, Somayeh Sadeghi, Ziba Farajzadegan, Sylvia Hovsepian, Rezvaneh Hadian
Publikováno v:
مجله دانشکده پزشکی اصفهان, Vol 25, Iss 87 (2011)
مقدمه: كمكاری مادرزادی تیروئید با شیوع قابل توجه در كشور ما، در صورت عدم درمان یا تأخیر در آن، آثار نامطلوب و جبرانناپذیری برجا میگذ
Externí odkaz:
https://doaj.org/article/840bbcd766be41ea93e4f687685a9814
Autor:
Mahin Hashemipour, Mahmoud Ghasemi, Silva Hovsepian, Kamal Heiydari, Ali Sajadi, Rezvaneh Hadian, Marjan Mansourian, Naghme Mirshahzadeh, Roya Kelishadi, Marzie Dalvi
Publikováno v:
Advanced Biomedical Research, Vol 3, Iss 1, Pp 21-21 (2014)
Background: Considering the higher prevalence of congenital hypothyroidism (CH) in Iran and the importance of determination of the etiology of CH for assessing appropriate treatment strategies, understanding the pathogenesis of CH and the implication
Externí odkaz:
https://doaj.org/article/0bd9a69c0d7148efa96bb67db52c9760
Autor:
Mahmoud, Ghasemi, Mahin, Hashemipour, Silva, Hovsepian, Kamal, Heiydari, Ali, Sajadi, Rezvaneh, Hadian, Marjan, Mansourian, Naghme, Mirshahzadeh, Marzie, Dalvi
Publikováno v:
Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences
Background: Congenital hypothyroidism (CH) considered a common endocrine disorder in Iran. We report the epidemiologic findings of CH screening program in Isfahan, seven years after its development, regarding the prevalence of transient CH (TCH) and
Autor:
Fahimeh Soheilipour, Sakineh Karimizare, Massoud Amini, Hossein Khanahmad, Morteza Karimipour, Mahin Hashemipour, Silva Hovsepian, Rezvaneh Hadian, Leila Kokabee, Sepideh Aminzadeh
Publikováno v:
Int J Endocrinol
Int J Endocrinol, 2012, 2012, pp.717283. ⟨10.1155/2012/717283⟩
International Journal of Endocrinology, Vol 2012 (2012)
International Journal of Endocrinology
Int J Endocrinol, 2012, 2012, pp.717283. ⟨10.1155/2012/717283⟩
International Journal of Endocrinology, Vol 2012 (2012)
International Journal of Endocrinology
Background. Thyroid peroxidase gene (TPO) mutations are one of the most common causes of thyroid dyshormonogenesis in patients with congenital hypothyroidism (CH). In this study, the prevalence of TPO gene mutations in patients with thyroid dyshormon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46c988166d5598943abda7b2f2c2802e
https://hal-riip.archives-ouvertes.fr/pasteur-00826038/document
https://hal-riip.archives-ouvertes.fr/pasteur-00826038/document