Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Sima Sedighi"'
Autor:
Mohammadrafi Damirchi, Mehrdad Aghaie, Sima Sedighi, Samaneh Tavassoli, Gholamreza Roshandel, Mohammadjavad Hassani, Nafiseh Abdolahi
Publikováno v:
Iranian Journal of Medical Sciences, Vol 48, Iss 1, Pp 91-97 (2023)
Recently, due to the coronavirus disease 2019 (COVID-19) pandemic, much concern has been raised about patients with chronic diseases who may become more susceptible to the disease. The present cross-sectional study aimed to characterize the clinical
Externí odkaz:
https://doaj.org/article/40d4f5f1f1f641609a767f0354b7584a
Publikováno v:
Avicenna Journal of Phytomedicine, Vol 11, Iss 4, Pp 314-323 (2021)
Objective: Acute promyelocytic leukemia (APL) is among the most threatening hematological malignant cancers. Defects in cell growth and apoptotic pathways lead to the pathogenesis of the disease as well as its resistance to therapy; therefore, it is
Externí odkaz:
https://doaj.org/article/8223d1f51dab4a53b6a7a792d14696ae
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 29, Iss 2, Pp 3453-3461 (2021)
Introduction: Hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) is an autosomal dominant genetic disease. The disease is caused by a mutation in one of four genes of the DNA mismatch repair system and increases the risk for various ca
Externí odkaz:
https://doaj.org/article/9e67943e85cc4de1ba0e1b4f9876f986
Publikováno v:
Tehran University Medical Journal, Vol 78, Iss 7, Pp 407-415 (2020)
Familial adenomatous polyposis is characterized by over 100 colorectal adenomas in the colorectum. The disease equally affects both sexes, with an incidence estimated at 1.14025-1.8300. The disease is premature in people with familial adenomatous pol
Externí odkaz:
https://doaj.org/article/1aa30a7f081540eca54902f6d592c299
Publikováno v:
Majallah-i Dānishgāh-i ’Ulūm-i Pizishkī-i Shahīd Ṣadūqī Yazd, Vol 28, Iss 6, Pp 2720-2733 (2020)
Introduction: Hamartomatous Polyposis Syndromes (HPS) are a rare group of dominant autosomal inheritance, which is characterized by the development of hamartomatous polyps in the gastrointestinal tract. This syndrome included Juvenile Polyposis synd
Externí odkaz:
https://doaj.org/article/bf74bbd67637459793c299ae70cfe1d7
Publikováno v:
Iranian Journal of Pathology, Vol 14, Iss 3, Pp 236-242 (2019)
Background & Objective: Systemic lupus erythematosus (SLE) is an autoimmune disease with chronic inflammatory immune response. Current therapies mostly rely on glucocorticoids which are accompanied by side-effects and mostly fail to achieve a favorab
Externí odkaz:
https://doaj.org/article/6df4d8aa1e8b40b5ad6077725539cc17
Publikováno v:
Middle East Journal of Digestive Diseases, Vol 11, Iss 1, Pp 5-16 (2019)
Therapeutic targeting of phosphatidyl-inositol 3-kinase (PI3K) is considered as a possible strategy in several types of cancer, including gastrointestinal ones. In vitro and in vivo studies indicated the significance of proapoptotic and antiprolifera
Externí odkaz:
https://doaj.org/article/4c7f8e3f52554008bab2d709147bedd4
Autor:
Ahmadreza Jamshidi, Farhad Gharibdoost, Sima Sedighi, Asghar Hajiabbasi, Amir-Hossein Salari, Alireza Khabbazi, Peyman Mottaghi, Ahmad Tahammoli Roudsari, Mehrdad Aghaei, Irandokht Shenavar Masooleh, Araz Sabzvari, Nassim Anjidani
Publikováno v:
Journal of Osteoporosis, Vol 2021 (2021)
The safety of teriparatide has been studied in various phase III and phase IV trials. However, a postmarketing study of the biosimilar of teriparatide, CinnoPar®, has not been conducted on Iranian patients. This was a phase IV study conducted on ost
Externí odkaz:
https://doaj.org/article/6bacbac1106f4ce6bc80a06c1a80a857
Autor:
Zahra Rezaieyazdi, Mina AkbariRad, Nayyereh Saadati, Masoumeh Salari, Reza Orang, Sima Sedighi, Habibollah Esmaily, Mahmoud Reza Azarpazhooh, Abdollah Firoozi, Ensieh Akbarpour
Publikováno v:
ARYA Atherosclerosis, Vol 17, Iss 1, p 2126 (2022)
BACKGROUND: Interleukin-18 (IL-18) is a pro-inflammatory and pro-atherogenic factor, and its blood level has shown a direct correlation with atherosclerosis. We aimed to evaluate the serum IL-18 level in patients with systemic lupus erythematosus (SL
Externí odkaz:
https://doaj.org/article/477aee8eb04d42b490bec4473ee5e3ec
Publikováno v:
مجله دانشگاه علوم پزشکی گرگان, Vol 20, Iss 3, Pp 99-103 (2018)
Background and Objective: Systemic lupus erythatous (SLE) is an autoimmune disease with clinical symptoms. Anti neutrophil cytoplasmic antibody (ANCA) is common in vasculitis which is reported in SLE. This study was done to determine the frequency of
Externí odkaz:
https://doaj.org/article/26f6ca7c43d04af9a5a870761d7df83d