Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Imen, Sassi"'
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-4 (2024)
Abstract Background Neurofibromatosis type 1 is a neurocutaneous genetic disorder caused by mutations in the NF1 gene, resulting in the formation of benign tumors called neurofibromas. The most common type of tumor seen in patients with neurofibromat
Externí odkaz:
https://doaj.org/article/6684c32409bb4c5598bea99b9db855b8
Autor:
Nesrine Chraiet, Yosr Zenzri, Hanen Bouaziz, Imen Sassi, Azza Guebsi, Salma Kamoun, Khaled Rahal, Amel Mezlini
Publikováno v:
Clinical Case Reports, Vol 8, Iss 4, Pp 667-671 (2020)
Abstract Cutaneous metastases are rare and represent a sign of poor prognosis. They are a sign of widespread disease. Breast cancer is the most common neoplasm leading to their appearance. Palliative care is the treatment of choice.
Externí odkaz:
https://doaj.org/article/ad38b3e344704392bfa21db952cd4031
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
Autor:
Imen, Sassi, Nayssem, Khessairi, Amine, Bouida Mohamed, Anis, Hasnaoui, Nadia, Boujelbene, Tarek, Ben Dhieb
Publikováno v:
In International Journal of Surgery Case Reports September 2023 110
Autor:
Sassi, Imen1 (AUTHOR) imen.sassi.mail@gmail.com, Bouida, Mohamed Amine1 (AUTHOR), Hasnaoui, Anis2 (AUTHOR), Zemni, Ines1 (AUTHOR), Ben Dhieb, Tarek1 (AUTHOR)
Publikováno v:
Journal of Medical Case Reports. 1/13/2024, Vol. 18 Issue 1, p1-4. 4p.
Autor:
Hasnaoui, Anis1,2 hasnaouianis001@gmail.com, Trigui, Racem1, Heni, Sihem1, Kammoun, Houda1, Sassi, Imen3
Publikováno v:
Pan African Medical Journal. May-Aug2023, Vol. 45, p1-6. 6p.
Autor:
Chraiet, Nesrine1 (AUTHOR) nesrinechraiet@gmail.com, Zenzri, Yosr1 (AUTHOR) yosr-zenzri@live.fr, Bouaziz, Hanen2 (AUTHOR), Sassi, Imen2 (AUTHOR), Guebsi, Azza1 (AUTHOR), Kamoun, Salma3 (AUTHOR), Rahal, Khaled2 (AUTHOR), Mezlini, Amel1 (AUTHOR)
Publikováno v:
Clinical Case Reports. Apr2020, Vol. 8 Issue 4, p667-671. 5p.
Autor:
Bouhani, Malek, Sassi, Imen, Zemni, Ines, Sahraoui, Ghada, Bouida, Amine, Slimene, Maher, Rahal, Khaled
Publikováno v:
SAGE Open Medical Case Reports; 6/4/2021, Vol. 9, p1-6, 6p
Publikováno v:
Genomics & Genetics Weekly; 2/2/2024, p1647-1647, 1p
Autor:
Nouira, Semir, Boukef, Riadh, Bouida, Wahid, Kerkeni, Wieme, Beltaief, Kaouther, Boubaker, Hamdi, Boudhib, Latifa, Grissa, Mohamed, Trimech, Mohamed, Boussarsar, Hamadi, Methamem, Mehdi, Marghli, Soudani, Ltaief, Mondher
Publikováno v:
Intensive Care Medicine; Feb2011, Vol. 37 Issue 2, p249-256, 8p, 1 Diagram, 3 Charts, 2 Graphs