Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Samira Saee Rad"'
Autor:
Ghasem Fakhraie, Wayne K. Greene, Samira Saee Rad, Reza Raoofian, Sevil Aghapour, Navid Nilforoushan, Mansour Heidari
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 3, Pp 208-212 (2012)
Glaucoma is a major cause of blindness worldwide. A single nucleotide polymorphism of the MTHFR gene (C677T) has been associated with susceptibility to this disease, although this is controversial in the last decade. In this study, the possible assoc
Externí odkaz:
https://doaj.org/article/e898276d98cf4b559c645dd9001f2f06
Autor:
Navid Nilforoushan, Sevil Aghapour, Reza Raoofian, Samira Saee Rad, Wayne K. Greene, Ghasem Fakhraie, Mansour Heidari
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 3 (2012)
Glaucoma is a major cause of blindness worldwide. A single nucleotide polymorphism of the MTHFR gene (C677T) has been associated with susceptibility to this disease, although this is controversial in the last decade. In this study, the possible assoc
Externí odkaz:
https://doaj.org/article/3c6f63fe6b724b6287551dc49727a300
Autor:
Maryam Hedayat, Mina Ataei, Niloufar Jafari Namini, Samira Saee Rad, Jalal Rezaei, Banfsheh Mashak
Publikováno v:
International Journal of Psychosocial Rehabilitation. 24:1398-1406
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5297725b7ad36e44427437f1c064a51
https://doi.org/10.37200/ijpr/v24i3/pr200889
https://doi.org/10.37200/ijpr/v24i3/pr200889
Autor:
Mina Ataei, Maryam Mirzaei, Farshid Inanloo, Narges Maleki, Samira Saee Rad, Seyedeh Mastooreh Noorbakhsh, Atousa Karimi
Introduction and objective: The mechanism of natural killer (NK) cells is based on the recognition of insider cells from alien cells according to inhibitory and activator responses of the receptor. One group of natural killer cell receptors are the k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f431aa1b3402a02a3a763964f3c6942
Autor:
Saeed Nikkhah, Mostafa Qorbani, Samira Saee Rad, Kumars Pourrostami, Mehri Golami, Nasrin Elahimehr, Ehsan Zahmatkesh, Esfandiar Najafi Tavana, Reza Arjmand, Omid Safari, Kimia Seifi, Fariba Shirvani
Publikováno v:
Archives of Pediatric Infectious Diseases. 7
Background: The administration of Haemophilus influenzae type b (Hib) conjugate vaccine led to a decrease of over 90% in the prevalence of severe Hib diseases in the countries with universal coverage vaccine. After addition of Hib vaccine to the nati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::805e82a84a55f293dbf1e8e889fe43da
https://doi.org/10.5812/pedinfect.82238
https://doi.org/10.5812/pedinfect.82238
Autor:
Mina Ataei, Samira Saee Rad, Aida Borzabadi, Seyyed Mohsen Pouryaghobi, Banafsheh Mashak, Mehdi Rezaee
Publikováno v:
Electronic Journal of General Medicine. 17:em199
Introduction: One of the most common complications of spinal anesthesia in elective cesarean is a headache, known commonly as post-dural-puncture headache (PDPH). Various methods are mainly recommended such as resting and the use of non-opioid analge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c5d4bf7506a1b9bf785cf03596ab6fa
https://doi.org/10.29333/ejgm/7847
https://doi.org/10.29333/ejgm/7847
Autor:
Maryam, Beheshtian, Samira, Saee Rad, Mojgan, Babanejad, Marzieh, Mohseni, Hassan, Hashemi, Arash, Eshghabadi, Fedra, Hajizadeh, Mohammad Reza, Akbari, Kimia, Kahrizi, Mohammad, Riazi Esfahani, Hossein, Najmabadi
Publikováno v:
Archives of Iranian medicine. 18(11)
Non-syndromic autosomal recessive Retinitis Pigmentosa (arRP) is a highly heterogeneous genetic visual disorder with a large number of causative genes. We aimed to determine the power of Whole Exome Sequencing (WES) in the identification of the genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67f131b5f7b6e5f635f53bf759ca6e96
https://pubmed.ncbi.nlm.nih.gov/26497376
https://pubmed.ncbi.nlm.nih.gov/26497376
Autor:
Samira, Saee-Rad, Hassan, Hashemi, Mohammad, Miraftab, Mohammad Reza, Noori-Daloii, Morteza Hashemzadeh, Chaleshtori, Reza, Raoofian, Fatemeh, Jafari, Wayne, Greene, Ghasem, Fakhraie, Farhad, Rezvan, Mansour, Heidari
Publikováno v:
Molecular Vision
Purpose To evaluate mutations in the visual system homeobox gene 1 (VSX1) and superoxide dismutase 1 (SOD1) genes with keratoconus (KTCN), direct sequencing was performed in an Iranian population. Methods One hundred and twelve autosomal dominant KTC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::908017e08f9eb6251e13ff3f468a8042
https://pubmed.ncbi.nlm.nih.gov/22171159
https://pubmed.ncbi.nlm.nih.gov/22171159
Autor:
Mansour Heidari, Samira Saee-Rad, Kazem Zendehdel, Reza Raoofian, Ramesh Omranipour, Cyrus Azimi, Babak Rahmani
Publikováno v:
Acta Medica Iranica, Vol 50, Iss 7, Pp 447-453 (2012)
The mitochondrial DNA (mtDNA) mutations in mitochondrial coding and non coding regions seem to be important in carcinogenesis. The aim of this investigation was to evaluate coding region (mt-tRNAPhe and tRNAPro) and non-coding sequence, mitochondrial
Externí odkaz:
https://doaj.org/article/734247fb184b47e4ba4c38c94b728fed
Autor:
Reza Raoofian, Mohammad Reza Noori-Daloii, Samira Saee-Rad, Mohammad Hossein Modarresi, Seyed Hamid Ghaffari, Majid Mojarrad, Farid Abolhasani, Mansour Heidari
Publikováno v:
Acta Medica Iranica, Vol 51, Iss 12 (2013)
Glioblastoma is the most common and the most lethal primary brain cancer. This malignancy is highly locally invasive, rarely metastatic and resistant to current therapies. Little is known about the distinct molecular biology of glioblastoma multiform
Externí odkaz:
https://doaj.org/article/1ee68577cbfc46e584bd28bf5eff4e18