Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sajjad Biglari"'
Autor:
Sajjad Biglari, Hassan Vahidnezhad, Mohammad Amin Tabatabaiefar, Hamid Reza Khorram Khorshid, Emran Esmaeilzadeh
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 12, Iss 4, Pp n/a-n/a (2024)
Abstract Background Hypomyelinating leukodystrophy‐9 (HLD‐9) is caused by biallelic pathogenic variants in RARS1, which codes for the cytoplasmic tRNA synthetase for arginine (ArgRS). This study aims to evaluate the clinical, neuroradiological, a
Externí odkaz:
https://doaj.org/article/3db4072ee00842fd85063a977604b46b
Autor:
Leila Youssefian, Sajjad Biglari, Atefeh Sohanforooshan Moghaddam, Amir Hossein Saeidian, Fatemeh Vahidnezhad, Hassan Vahidnezhad
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101660- (2024)
Externí odkaz:
https://doaj.org/article/30ef90709d44443f872d3c921b70457c
Autor:
Flor Fakour, Minoosh Moghimi, Abdolreza Esmaeilzadeh, Faranak Kalantari, Fatemeh Eskandari, Sajjad Biglari, Saeideh Mazloomzadeh
Publikováno v:
Middle East Journal of Cancer, Vol 13, Iss 1, Pp 81-88 (2022)
Background: The protective role of vitamin D in the occurrence of breast cancer is nowadays a controversial matter. Based on conflicting results of the studies in this field and also considering the prevalence of vitamin D deficiency in Iranian women
Externí odkaz:
https://doaj.org/article/8761dd53875e4261a05462787dfac145
Autor:
Mehran Yousefi, Mehdi Panahali, Kamran Azarkhish, Nazanin Azizi Shalbaf, Sajjad Biglari, Zahra Jor-Ahmad, Mehdi Maghbooli
Publikováno v:
Romanian Journal of Neurology, Vol 20, Iss 1, Pp 35-40 (2021)
Background. The 2010 revision of the McDonald criteria, widely used for the diagnosis of multiple sclerosis (MS), has established that dissemination in time (DIT) can be demonstrated by the simultaneous presence of asymptomatic gadolinium-enhancing a
Externí odkaz:
https://doaj.org/article/704c3764501140d5b949a44a3db64d39
Autor:
Mehrdad Nasrollahzadeh Sabet, Mohammad Foad Heidari, Mohammad Khanalipour, Saadat Allah Ghaffari, Milad Jafari Ashiani, Sajjad Biglari, Emran Esmaeilzadeh
Publikováno v:
Majallah-i dānishgāh-i ̒ulūm-i pizishkī-i Arāk, Vol 23, Iss 5, Pp 766-773 (2020)
Background and Aim: Since late 2019, with the emergence of a new type of coronavirus that causes a new respiratory disease called COVID-19, there have been many concerns about the spread of this disease and how to deal with it. Due to the ability of
Externí odkaz:
https://doaj.org/article/ec1ebc6c936643c9b026fcf8df7a9324
Autor:
Mehdi Maghbooli, Abdolreza Esmaeilzadeh, Fatemeh Karami Zarandi, Arezoo Jafarzadeh, Sajjad Biglari, Nazanin Azizi Shalbaf, Negar Farhoudi
Publikováno v:
Acta Medica Lituanica, Vol 28, Iss 2 (2021)
Background: Bell’s palsy is the most common cause of peripheral facial palsy. The etiology and treatment of Bell’s palsy are still controversial. Previous studies emphasize the role of herpes simplex and herpes zoster viruses in this ailment. The
Externí odkaz:
https://doaj.org/article/ada309c2a3ce4ed2a03da27f4c84fbf6
Autor:
Sajjad Biglari, Mehdi Maghbooli, Nazanin Azizi Shalbaf, Kamran Azarkhish, Mehdi Panahali, Zahra Jor-Ahmad, Mehran Yousefi
Publikováno v:
Romanian Journal of Neurology, Vol 20, Iss 1, Pp 35-40 (2021)
Background. The 2010 revision of the McDonald criteria, widely used for the diagnosis of multiple sclerosis (MS), has established that dissemination in time (DIT) can be demonstrated by the simultaneous presence of asymptomatic gadolinium-enhancing a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e734c2f7bc45d78ad795cb3588d5c460
https://rjn.com.ro/articles/2021.1/RJN_2021_1_Art-05.pdf
https://rjn.com.ro/articles/2021.1/RJN_2021_1_Art-05.pdf
Autor:
Mohammad Hassan Ghadiani, Hossein Jafari, Mohsen Nafar, Fatemeh Hajirezaei, Sayyed Mohammad Hossein Ghaderian, Mandana Hasanzad, Sajjad Biglari, Nasim Sohrabifar
Publikováno v:
Reports of Biochemistry and Molecular Biology. 9:193-198
Background Autosomal dominant polycystic kidney disease (ADPKD), a multisystem disorder, is the most prevalent type of hereditary kidney disease. Here, we aimed to evaluate methylation of the PKD1 gene (PKD1) promoter and its correlation with PKD1 ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18986f97bb78c2ec2fcbeeecd59bc078
https://doi.org/10.29252/rbmb.9.2.193
https://doi.org/10.29252/rbmb.9.2.193
Autor:
Sajjad Biglari, Alireza Shoghli, Abdolreza Esmaeilzadeh, Negin Parsamanesh, Malihe Mohamadian, Hossein Chiti
Publikováno v:
The Journal of Gene Medicine
Background At the end of December 2019, a novel coronavirus tentatively named SARS‐CoV‐2 in Wuhan, a central city in China, was announced by the World Health Organization. SARS‐CoV‐2 is an RNA virus that has become a major public health conce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15d46d10f97c09b047ae946e779174d3
https://doi.org/10.1002/jgm.3303
https://doi.org/10.1002/jgm.3303
Autor:
Fatemeh, Hajirezaei, Sayyed Mohammad Hossein, Ghaderian, Mandana, Hasanzad, Mohsen, Nafar, Mohammad Hasan, Ghadiani, Sajjad, Biglari, Nasim, Sohrabifar, Hossein, Jafari
Publikováno v:
Rep Biochem Mol Biol
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD), a multisystem disorder, is the most prevalent type of hereditary kidney disease. Here, we aimed to evaluate methylation of the PKD1 gene (PKD1) promoter and its correlation with PKD1 e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f55dce7ac7f887cc458bc2f42fbd16ca
https://pubmed.ncbi.nlm.nih.gov/33178869
https://pubmed.ncbi.nlm.nih.gov/33178869