Zobrazeno 1 - 10
of 60
pro vyhledávání: '"GHADA SAHRAOUI"'
Autor:
Nour-elhouda Neili, Zaineb AbdelKafi-Koubaa, Jed Jebali, Khouloud Kaidi, Ghada Sahraoui, Melika Ben Ahmed, Najet Srairi-Abid, Naziha Marrakchi, Raoudha Doghri, Ines ELBini
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-17 (2024)
Abstract Several neurodegenerative diseases, such as multiple sclerosis and Parkinson’s disease, are linked to alterations in myelin content or structure. Transmembrane receptors such as integrins could be involved in these alterations. In the pres
Externí odkaz:
https://doaj.org/article/e33fe32871b24e25b2cae58504b7b33c
Autor:
Aida Jlassi, Rim Rejaibi, Maroua Manai, Ghada Sahraoui, Fatma Zahra Guerfali, Lamia Charfi, Amel Mezlini, Mohamed Manai, Karima Mrad, Raoudha Doghri
Publikováno v:
Frontiers in Oncology, Vol 14 (2024)
IntroductionImmunotherapy by blocking immune checkpoints programmed death/ligand (PD1/PDL1) and cytotoxic T-lymphocyte-associated protein 4(CTLA4) has emerged as new therapeutic targets in cancer. However, their efficacy has been limited due to resis
Externí odkaz:
https://doaj.org/article/cb33d3647301400aae5d4036db415272
Publikováno v:
Rare Tumors, Vol 15 (2023)
Introduction: Primary cutaneous CD8+ acral T-cell lymphoproliferative disorder (CD8+ ATCLPD) is a rare form of cutaneous T-cell lymphoma that commonly presents on the acral regions of the body. We report a case of a 61-year-old man diagnosed with pri
Externí odkaz:
https://doaj.org/article/1d228d93810d40e5bfbd73174061437c
Autor:
Takoua Chalouati, Montassar Ghalleb, Amani Jallali, Maher Slimane, Ghada Sahraoui, Jamal Ben hassouna, Riadh Chargui, Khaled Rahal
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-6 (2022)
Abstract Introduction Paratesticular rhabdomyosarcoma is a rare and aggressive mesenchymal tumor, accounting for only 7% of all rhabdomyosarcomas. It is mainly encountered in children and adolescents. The standard treatment consists of radical orchid
Externí odkaz:
https://doaj.org/article/9349f233c44c428c82a347c4af7924ed
Publikováno v:
Rare Tumors, Vol 15 (2023)
Introduction: Follicular dendritic cell sarcomas (FDCS) are rare tumours, typically seen in lymph nodes. However, in about one third of the reported cases, a FDCS presents as an extranodal mass. Involvement of the gastrointestinal tract is rare, and
Externí odkaz:
https://doaj.org/article/6b0c9d7805e34e5eb592c2fcaacfa6a4
Autor:
Aida Jlassi, Maroua Manai, Maram Morjen, Ghada Sahraoui, Monia Elasmi Allal, Ines ELBini-Dhouib, Lamia Naija, Lamia Charfi, Rim Rejaibi, Melika Ben Ahmed, Naziha Marrakchi, Najet Srairi-Abid, Amel Mezlini, Mohamed Manai, Karima Mrad, Raoudha Doghri
Publikováno v:
PLoS ONE, Vol 18, Iss 3, p e0278849 (2023)
Immunotherapy by blocking immune checkpoint regulators has emerged as a new targeted therapy for some cancers. Among them V-domain Ig suppressor of Tcell activation (VISTA) which is identified as a novel checkpoint regulator in ovarian cancer. This s
Externí odkaz:
https://doaj.org/article/376c2063d6374966ae4a76ec9738ef8c
Publikováno v:
Educación Médica, Vol 24, Iss 1, Pp 100776- (2023)
Introduction: Distance learning (DL) is a promising educational approach for teaching medical courses. Our Pathology College was faced with the difficulty of a complete online transition of the classes because of the public health measures implemente
Externí odkaz:
https://doaj.org/article/e4715a609c6a454d904fe9e1f342078f
Publikováno v:
Rare Tumors, Vol 14 (2022)
Myxoid liposarcoma (MLPS) is the second most prevalent subtype of liposarcoma. It is usually found in the deep tissues of the lower limbs and rarely in gynecologic tract. Herein we present the second case in the English literature of a primary MLPS a
Externí odkaz:
https://doaj.org/article/628373a33e72460bb34ac5fb04bd8cbb
Autor:
Azza Gabsi, Yosr Zenzri, Ghada Sahraoui, Ihsen Ben Brahim, Mouna Cherif, Yosra Yahyaoui, Nesrine Chraiet, Karima Mrad, Achraf Chedly, Anis Ben Maamer, Amel Mezlini
Publikováno v:
Clinical Case Reports, Vol 8, Iss 7, Pp 1130-1133 (2020)
Abstract The gastric location of EBVMCU is extremely rare. The pathology examination and immunochemistry are mandatory for the diagnosis. It is essential that physicians be aware of this new entity to accurately diagnose and handle this disease.
Externí odkaz:
https://doaj.org/article/ad23e8117b754081a0f5471eaf7448be
Autor:
Malek Bouhani, Imen Sassi, Ines Zemni, Ghada Sahraoui, Amine Bouida, Maher Slimene, Khaled Rahal
Publikováno v:
SAGE Open Medical Case Reports, Vol 9 (2021)
Ewing’s sarcoma/primitive neuroectodermal tumor is rare and aggressive with a poor prognosis. Intraabdominal metastases are an uncommon condition. Metastasis in the lesser sac is an exceptional occurrence. To the best of our knowledge, this locatio
Externí odkaz:
https://doaj.org/article/e6119562047644b381f13a9951094ead