Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Parisa Mokhles"'
Autor:
Parisa Mokhles, Alireza Sadeghipour, Pegah Babaheidarian, Saleh Mohebbi, Zahra Keshtpour Amlashi, Mohammad Hadi Gharib, Mohammad Saeid Ahmadi, Zeinab Khastkhodaei
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-9 (2024)
Abstract Background Secretory carcinoma (SC) has been described as a distinct salivary gland tumor in the fourth edition of the World Health Organization (WHO) classification of head and neck tumors. SC is generally considered as a slow-growing low-g
Externí odkaz:
https://doaj.org/article/db305cbfc892404e8c69a87956d3c2b6
Autor:
Amir Reza Eghtedari, Mohammad Amin Vaezi, Elaheh Safari, Vahid Salimi, Banafsheh Safizadeh, Pegah Babaheidarian, Amene Abiri, Elmira Mahdinia, Alireza Mirzaei, Parisa Mokhles, Masoumeh Tavakoli-Yaraki
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-15 (2023)
Abstract The expression pattern, diagnostic value, and association of PD-L1, IFN-γ and TGF-β with bone tumor type, severity, and relapse are determined in this study. 300 human samples from patients with osteosarcoma, Ewing sarcoma, and GCT were en
Externí odkaz:
https://doaj.org/article/6b933bc5b1a743e49a1923e45bb93f20
Autor:
Pegah Babaheidarian, Parisa Mokhles, Saleh Mohebbi, Razieh Shahnazari, Nasser Karimi, Donya Ghazinia, Sina Karaji, Shahriar Shirzadi
Publikováno v:
Cancer Reports, Vol 7, Iss 4, Pp n/a-n/a (2024)
Abstract Background Psammomatoid ossifying fibroma (POF) is a rare craniofacial neoplasm, primarily affecting the maxillofacial region, and typically observed in adolescents and young adults. This case report presents a unique occurrence of POF in a
Externí odkaz:
https://doaj.org/article/27f8b494321c4789931bdfdb0ea1ac7d
Autor:
Razieh Shahnazari, Shahriar Shirzadi, Sina Karaji, Parisa Mokhles, Mohamad Javad Ghafouri Far, Salome Maghsudlu
Publikováno v:
Clinical Case Reports, Vol 12, Iss 1, Pp n/a-n/a (2024)
Key Clinical Message Endometrial Carcinoma Arising from Adenomyosis (EC‐AIA) is an unusual condition, primarily occurring in postmenopausal women. We present a rare case of a 34‐year‐old woman with EC‐AIA, highlighting the diagnostic challeng
Externí odkaz:
https://doaj.org/article/ddb43d16d721442da1c56c5ea758aa48