Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Rojina Alimoghadam"'
Autor:
Shaya Alimoghadam, Arvin Eslami, Rojina Alimoghadam, Ibrahim Bahrami Mianrood, Mehdi Azizmohammad Looha, Sanaz Khodadadi, Shervin Shokouhi, Ilad Alavi Darazam
Publikováno v:
Journal of Global Antimicrobial Resistance, Vol 39, Iss , Pp 159-169 (2024)
Objectives: Pseudomonas aeruginosa is a major opportunistic pathogen responsible for a wide range of infections. The emergence of antibiotic resistance in this pathogen poses a significant public health challenge. This study aims to conduct a compreh
Externí odkaz:
https://doaj.org/article/f9d921794b7e4468af031202d36ba80e
Autor:
Hamidreza Yazdi, Arvin Eslami, Ali Torkaman, Omid Elahifar, Amir Kasaeian, Shaya Alimoghadam, Rojina Alimoghadam, Mansour Abolghasemian
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-10 (2024)
Abstract Objective The optimal agent for thromboprophylaxis following arthroscopic anterior cruciate ligament reconstruction (ACLR) remains unclear, particularly in patients with a low baseline risk for venous thromboembolism (VTE). This retrospectiv
Externí odkaz:
https://doaj.org/article/f656c439f60a4515b1f6383f1df734a4
Autor:
Mehrdad Mozafar, Sina Kazemian, Elahe Hoseini, Mohammad Mohammadi, Rojina Alimoghadam, Mahan Shafie, Mahsa Mayeli
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 8, Iss , Pp 100177- (2023)
Background: Blood uric acid level indicates an emerging biomarker in Parkinson's disease (PD). This study aimed to evaluate longitudinal uric acid levels among different kinds of glucocerebrosidase (GBA) mutations and to compare it among sporadic PD,
Externí odkaz:
https://doaj.org/article/ccba40911e9b450489a2b05feae32fed
Autor:
Mehrdad Mozafar, Sina Kazemian, Elahe Hoseini, Mohammad Mohammadi, Rojina Alimoghadam, Mahan Shafie, Mahsa Mayeli
Publikováno v:
Clinical parkinsonismrelated disorders. 8
Blood uric acid level indicates an emerging biomarker in Parkinson's disease (PD). This study aimed to evaluate longitudinal uric acid levels among different kinds of glucocerebrosidase (GBA) mutations and to compare it among sporadic PD, genetic coh