Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Farzane, Zare Ashrafi"'
Autor:
Hanieh Behravan, Ahmad Piroozmand, Azam Ghaziasadi, Khadijeh Jalalvand, Mahdieh Koshki, Fatemeh Tavangar, Angila Ataei-Pirkooh, Farid Yousefi, Masoumeh Bayani, Zohreh Fattahi, Hamed Fakhim, Mojtaba Varshochi, Mohammad Khazeni, Zakiye Mokhames, Fariba Shahraki-Sanavi, Reza Malekzadeh, Maryam Beheshtian, Yousef Yahyapour, Seyed Jalal Kiani, Fariba Keramat, Shokouh Ghafari, Behrooz Ataei, Alireza Abdollahi, Afagh Moattari, Fatemeh Keshavarzi, Mohammad Reza Haghshenas, Alireza AnsariMoghaddam, Maryam Azad, Mohammad Hassan Pouriayevali, Mohsen Moghadami, Azarakhsh Azaran, Zohreh Elahi, Farhang Babamahmoodi, Mohamad Soveyzi, Kimia Kahrizi, Hamid Reza Khorram Khorshid, Vahdat Poortahmasebi, Reza Najafipour, Farzane Zare Ashrafi, Akram Ezani, Farid Azizi Jalilian, Mostafa Salehi-Vaziri, Seyed Mohammad Jazayeri, Seyed Mohammad Hashemi-Shahri, Abdolvahab Moradi, Ali Mojtahedi, Fatemeh Ghodratpour, Marzieh Mohseni, Davod Javanmard, Mahsa Tavakoli, Ali Jafarpour, Hossein Najmabadi, Alijan Tabarraei, Alireza Soleimani, Tahmineh Jalali, Elahe Nasri, Mahmood Yaghoubi, Marzieh Kalhor, Farah Bokharaei-Salim, Iman Rezaeiazhar, Masood Ziaee
Publikováno v:
Archives of Iranian Medicine. 25:508-522
SARS-CoV-2 genome surveillance projects provide a good measure of transmission and monitor the circulating SARS-CoV-2 variants at regional and global scales. Iran is one of the most affected countries still involved with the virus circulating in at l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::234661a7c997f97453fa3ecb1054d7e1
https://doi.org/10.34172/aim.2022.83
https://doi.org/10.34172/aim.2022.83
Autor:
Kimia Kahrizi, Hossein Najmabadi, Farzane Zare Ashrafi, Sanaz Arzhangi, Goli Kazemi, Marzieh Mohseni, Fariba Ardalani, Fatemeh Aghakhani Moghaddam, Fatemeh Peymani
Publikováno v:
Archives of Iranian Medicine. 23:842-847
Background: Recently, we have reported mutations in LARP7 gene, leading to neurodevelopmental disorders (NDDs), the most frequent cause of disability in children with a broad phenotype spectrum and diverse genetic landscape. Methods: Here, we present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e342f34c3e3f94ae9182084fcded167b
https://doi.org/10.34172/aim.2020.112
https://doi.org/10.34172/aim.2020.112
Autor:
Goli, Kazemi, Fatemeh, Peymani, Marzieh, Mohseni, Farzane, Zare Ashrafi, Sanaz, Arzhangi, Fariba, Ardalani, Fatemeh, Aghakhani Moghaddam, Kimia, Kahrizi, Hossein, Najmabadi
Publikováno v:
Archives of Iranian medicine. 23(12)
Recently, we have reported mutations in LARP7 gene, leading to neurodevelopmental disorders (NDDs), the most frequent cause of disability in children with a broad phenotype spectrum and diverse genetic landscape.Here, we present two Iranian patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e0ae230197f453936efbfe97cdabb3a
https://pubmed.ncbi.nlm.nih.gov/33356342
https://pubmed.ncbi.nlm.nih.gov/33356342