Zobrazeno 1 - 10
of 273
pro vyhledávání: '"Reza Bayat"'
Autor:
Ankita Kapoor, Reza Bayat Mokhtari, Sahithi Savithri Sonti, Riya Patel, Anthony George, Kristopher Attwood, Renuka Iyer, Sayan Chakraborty
Publikováno v:
Cancers, Vol 16, Iss 15, p 2719 (2024)
Hepatocellular carcinoma (HCC), the predominant form of liver cancer, is associated with high mortality rates both in the United States and globally. Despite current advances in immunotherapy regimens, there is a scarcity of biomarkers to guide thera
Externí odkaz:
https://doaj.org/article/9586e1f96685470e9088f4af18c1f1b1
Autor:
Shohreh Maleknejad, Setila Dalili, Ameneh Sharifi, Afagh Hassanzadeh Rad, Reza Bayat, Bahareh Rabbani, Nejat Mahdieh
Publikováno v:
International Journal of Endocrinology, Vol 2024 (2024)
Familial glucocorticoid deficiency is caused by variants in the MC2R and MRAP genes. We report an Iranian patient with congenital glucocorticoid deficiency and cholestasis due to pathogenic variants in the MC2R gene. This is the first documented case
Externí odkaz:
https://doaj.org/article/54a13b6b80f2438eb241494b03736e52
Autor:
Manijeh Tabrizi, Seyyedeh Azade Hoseini Nouri, Afagh Hasanzade Rad, Setila Dalili, Seyede Tahoura Hakemzadeh, Amir Mohammad Ghanbari, Reza Bayat, Amir Reza Mashaei, Nazanin Medghalchi, Kamyar Khosravi
Publikováno v:
Journal of Pediatrics Review, Vol 11, Iss 2, Pp 163-170 (2023)
Background: Bedside teaching is a concentrated form of small-group teaching that takes place in the presence of the patient. Improvement in communication skills in a sympathetic manner with the patient and the ability to provide a purposeful history
Externí odkaz:
https://doaj.org/article/31cbacc37e8e409f96e186d7ae6925d4
Autor:
Setila Dalili, Seyyedeh Azade Hoseini Nouri, Reza Bayat, Shahin Koohmanaee, Manijeh Tabrizi, Marjaneh Zarkesh, Alireza Tarang, Nejat Mahdieh
Publikováno v:
Human Genomics, Vol 17, Iss 1, Pp 1-6 (2023)
Abstract Background Mutations in NF1 gene could cause allelic disorders with clinical spectrum of Neurofibromatosis type 1 to Noonan syndrome. Here, a 7-year-old Iranian girl is described with Neurofibromatosis-Noonan syndrome due to a pathogenic var
Externí odkaz:
https://doaj.org/article/cc075eee30654e3784c217ff1b0fbc4b
Publikováno v:
مدلسازی و مدیریت آب و خاک, Vol 3, Iss 4, Pp 181-191 (2023)
Introduction Today, water security is one of the important limitations of development, especially in dry and desert areas. Because these areas not only have low rainfall, but also this low rainfall is not properly distributed. Despite the increase in
Externí odkaz:
https://doaj.org/article/0b2f2dde03d64d8bac971ec8c6f94ac0
Publikováno v:
محیط زیست و مهندسی آب, Vol 8, Iss 3, Pp 669-681 (2022)
Gully erosion is an important and major process of land destruction and is considered one of the most important sources of erosion and sediment production in the country. The purpose of this research was to determine the effect of saturated lime solu
Externí odkaz:
https://doaj.org/article/11762f88f2ad4ecf965bab05b55f4239
Autor:
Sasan Faridi, Reza Bayat, Aaron J. Cohen, Ensieh Sharafkhani, Jeffrey R. Brook, Sadegh Niazi, Mansour Shamsipour, Heresh Amini, Kazem Naddafi, Mohammad Sadegh Hassanvand
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract We estimated mortality and economic loss attributable to PM2·5 air pollution exposure in 429 counties of Iran in 2018. Ambient PM2.5-related deaths were estimated using the Global Exposure Mortality Model (GEMM). According to the ground-mon
Externí odkaz:
https://doaj.org/article/9beb9848452144c4bfebe29621af3907
Autor:
Setila Dalili, Reza Bayat, Seyyedeh Azade Hoseini Nouri, Shahin Koohmanaee, Manijeh Tabrizi, Marjaneh Zarkesh, Alireza Tarang
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100268- (2023)
Externí odkaz:
https://doaj.org/article/bb61dfd878804fdfa4ffd9e85b8b5260
Autor:
Shahin Koohmanaee, Seyyedeh Azadeh Hoseini Nouri, Vahid Aminzadeh, Manijeh Tabrizi, Reza Bayat, Fatemeh Kharaee, Maryam Shahrokhi, Afagh Hassanzadeh Rad, Saber Najafi Chakoosari, Setila Dalili, Ehsan Kazemnejad Leili
Publikováno v:
Caspian Journal of Neurological Sciences, Vol 9, Iss 1 (2023)
Background: Neuronal ceroid lipofuscinoses (NCL) is a rare progressive neurodegenerative disorder caused by more than 530 mutations of at least 13 different genes (CLN 1-14). NCL is a part of the lysosomal disease characterized by the presence of
Externí odkaz:
https://doaj.org/article/cfd2a7a53c8f4319be8462368a1ee2f9
Autor:
Reza Bayat, Abdollah Hosseini
Publikováno v:
پژوهشهای ترجمه در زبان و ادبیات عربی, Vol 12, Iss 26, Pp 297-323 (2022)
The issue of linguistic functions is considered one of the new subjects in linguistics, and it is noteworthy that these functions have a significant effect on the transmittance of meaning to receivers, maintenance of original language, more explanati
Externí odkaz:
https://doaj.org/article/79e58f655b714bfa804927787753f270