Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sanae Bennis"'
Autor:
Asmae Squalli Houssaini, Salma Lamrabet, Jean Paul Nshizirungu, Nadia Senhaji, Mohammed Sekal, Mehdi Karkouri, Sanae Bennis
Publikováno v:
Vaccines, Vol 12, Iss 6, p 655 (2024)
Glioblastoma (GBM) is the most common and aggressive malignant brain tumor. Standard treatments including surgical resection, radiotherapy, and chemotherapy, have failed to significantly improve the prognosis of glioblastoma patients. Currently, immu
Externí odkaz:
https://doaj.org/article/58c6b38ad46f4608ad500310a60af8cb
Autor:
Brahim El Hejjioui, Salma Lamrabet, Sarah Amrani Joutei, Nadia Senhaji, Touria Bouhafa, Moulay Abdelilah Malhouf, Sanae Bennis, Laila Bouguenouch
Publikováno v:
Diagnostics, Vol 13, Iss 11, p 1949 (2023)
Triple-negative breast cancer (TNBC) is a specific subtype of breast cancer lacking hormone receptor expression and HER2 gene amplification. TNBC represents a heterogeneous subtype of breast cancer, characterized by poor prognosis, high invasiveness,
Externí odkaz:
https://doaj.org/article/ed09771d649b4bdb933c96e0af36f04c
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 470 (2023)
Breast cancer is clinically and biologically heterogeneous and is classified into different subtypes according to the molecular landscape of the tumor. Triple-negative breast cancer is a subtype associated with higher tumor aggressiveness, poor progn
Externí odkaz:
https://doaj.org/article/98dc1af8f2524c94952bb24e11072d75
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 13, p 7474 (2022)
Glioblastoma is the most aggressive malignant tumor of the central nervous system with a low survival rate. The difficulty of obtaining this tumor material represents a major limitation, making the real-time monitoring of tumor progression difficult,
Externí odkaz:
https://doaj.org/article/422cf6922ae14a539cfe5a51c10f2008
Autor:
Nawal Hammas, Nadia Senhaji, My Youssef Alaoui Lamrani, Sanae Bennis, Elfaiz Mohamed Chaoui, Hind El Fatemi, Laila Chbani
Publikováno v:
Journal of Medical Case Reports, Vol 12, Iss 1, Pp 1-10 (2018)
Abstract Background Astroblastoma is a controversial and an extremely rare central nervous system neoplasm. Although its histogenesis has been clarified recently, controversies exist regarding its cellular origin and validity as a distinct entity. Be
Externí odkaz:
https://doaj.org/article/3297df8f7975419ba1fcdba10de208c0
Autor:
Laila Bouguenouch, Imane Samri, Meryem Abbassi, Hasna Hamdaoui, Ihssane El Otmani, Hanane Sayel, Said Trhanint, Sara Benmiloud, Moncif Amrani, Sanae Bennis, Karim Ouldim, Mustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 28, Iss 286 (2017)
L'anémie de Fanconi est une maladie récessive associée à une instabilité chromosomique, elle est marquée par une hétérogénéité phénotypique qui inclut une insuffisance médullaire, un syndrome malformatif variable, une prédisposition à
Externí odkaz:
https://doaj.org/article/705f1be34f42472c840423bdc2691a67
Autor:
Laila Bouguenouch, Imane Samri, Khadija Belhassan, Hanane Sayel, Meriame Abbassi, Sanae Bennis, Dafr Allah Benajah, Adil Ibrahimi, Afaf Amarti, Karim Ouldim
Publikováno v:
The Pan African Medical Journal, Vol 24, Iss 142 (2016)
Le syndrome de Lynch, ou cancer colorectal héréditaire sans polypose ou HNPCC (hereditary non-polyposis colorectal cancer), est la forme la plus fréquente de cancer colorectal héréditaire. Il conduit à une augmentation de la susceptibilité à
Externí odkaz:
https://doaj.org/article/69779e19152e440e8af1490eb9c53989
Autor:
Karim Ouldim, Laila Bouguenouch, Imane Samri, Ihsan El Otmani, Hasna Hamdaoui, Sanae Bennis, Mounia Idrissi Lakhdar, Sana Chaouki, Samir Atmani, Moustapha Hida
Publikováno v:
The Pan African Medical Journal, Vol 11, Iss 3 (2012)
Les syndromes microdélétionnels sont définis par la présence d'une anomalie chromosomique de taille mineure (inférieure à 5 mégabases) ou aneusomie segmentaire, décelable par cytogénétique moléculaire (FISH : Fluorescent in Situ Hybridizat
Externí odkaz:
https://doaj.org/article/387eb3e453944dfab9b6ce6eaa9baf23
Autor:
Nadia, Senhaji, Sara, Louati, Laila, Chbani, Sanae El, Bardai, Karima, Mikou, Mustafa, Maaroufi, Mohammed, Benzagmout, Mohammed Chaoui El, Faiz, Yannick, Marie, Karima, Mokhtari, Ahmed, Idbaih, Afaf, Amarti, Sanae, Bennis
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 17(5)
Genetic alterations in gliomas have increasing importance for classification purposes. Thus, we are especially interested in studying IDH mutations which may feature potential roles in diagnosis, prognosis and response to treatment. Our aim was to in
Autor:
Laila, Bouguenouch, Imane, Samri, Khadija, Belhassan, Hanane, Sayel, Meriame, Abbassi, Sanae, Bennis, Dafr Allah, Benajah, Adil, Ibrahimi, Afaf, Amarti, Karim, Ouldim
Publikováno v:
The Pan African Medical Journal
Le syndrome de Lynch, ou cancer colorectal héréditaire sans polypose ou HNPCC (hereditary non-polyposis colorectal cancer), est la forme la plus fréquente de cancer colorectal héréditaire. Il conduit à une augmentation de la susceptibilité à