Zobrazeno 1 - 10
of 111
pro vyhledávání: '"S. Sefiani"'
Autor:
N. Messaoudi, N. Bouichrat, M. Karrou, I. Assarrar, S. Malki, S. Elmahjoubi, S. Rouf, N. Karich, A. Lachkar, S. Sefiani, M. Bouziane, I. Kamaoui, H. Latrech
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Adrenal adenolipomas are rare lipomatous adrenal tumors that can be either functional or not. Only 7 cases have been reported in the English literature so far. However, brown tumors are benign, rare, historical lesions, with histological similarity t
Externí odkaz:
https://doaj.org/article/2079b5db2cf8461eb35202c997beb6df
Autor:
K. Quenum, J. Ntalaja, J. Onen, Y. Arkha, S. Derraz, A. El Ouahabi, S. Sefiani, A. ElKhamlichi
Publikováno v:
Case Reports in Neurological Medicine, Vol 2012 (2012)
Medulloblastoma is a relatively common malignant brain tumor of childhood and relatively rare in adulthood, with a propensity for neuraxial spread via cerebrospinal fluid pathways. Osseous extraneural metastasis is uncommon and when it happens, radio
Externí odkaz:
https://doaj.org/article/a7c7005e2e1b41889ed6652905b647fc
Autor:
I. Assarrar, S. Elmahjoubi, S. Sefiani, N. Karich, Hanane Latrech, I. Kamaoui, M. Karrou, A. Lachkar, M. Bouziane, Siham Rouf, S. Malki, N. Bouichrat, N. Messaoudi
Publikováno v:
Case Reports in Endocrinology
Case Reports in Endocrinology, Vol 2021 (2021)
Case Reports in Endocrinology, Vol 2021 (2021)
Adrenal adenolipomas are rare lipomatous adrenal tumors that can be either functional or not. Only 7 cases have been reported in the English literature so far. However, brown tumors are benign, rare, historical lesions, with histological similarity t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd0e1342a2be51fcd8768336b09561fc
https://doi.org/10.1155/2021/4870493
https://doi.org/10.1155/2021/4870493
Akademický článek
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Akademický článek
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Publikováno v:
Neurochirurgie. 58:254-257
The cerebral atypical rhabdoid/teratoid tumor constitutes one of the most aggressive tumors of children. Such tumors are equally characterized by a critically and speedly mortal development. The optimal management of such tumors remains unknown. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7b5623cccac5585e61cfb5afaedc769
https://doi.org/10.1016/j.neuchi.2012.02.003
https://doi.org/10.1016/j.neuchi.2012.02.003
Publikováno v:
Revue de Stomatologie et de Chirurgie Maxillo-faciale. 113:187-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7fc4d5be968d78107a7124425eaed0de
https://doi.org/10.1016/j.stomax.2012.01.010
https://doi.org/10.1016/j.stomax.2012.01.010
Autor:
A. Harmouch, S. Sefiani, M. El Khorassani, H. Charhi, M. Maher, A. Kili, M. El Khattab, N. Mansouri
Publikováno v:
Journal Africain du Cancer / African Journal of Cancer. 3:222-226
Rhabdomyosarcoma is the most common soft-tissue malignancy in the paediatric head and neck tumours. The objective of this study was to determine the epidemiological and pathological patterns of head and neck rhabdomyosarcoma in children in a Moroccan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71c418f486bba26c6bb1e8478fa58dd9
https://doi.org/10.1007/s12558-011-0182-9
https://doi.org/10.1007/s12558-011-0182-9
Autor:
O. Bakkacha, S. Sefiani, M.R. El Hassani, M. Jiddane, A. El Maroudi, H. Benchaaboune, A. Sqalli Houssaini, N. Chakir
Publikováno v:
Feuillets de Radiologie. 51:92-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::055d059f48bc3812c602b5f0ec436cb7
https://doi.org/10.1016/j.frad.2011.02.002
https://doi.org/10.1016/j.frad.2011.02.002
Publikováno v:
Journal Français d'Ophtalmologie. 34:133-137
Resume La tumeur fibreuse solitaire est une tumeur mesenchymateuse rare, plus frequemment observee au niveau de la plevre. La localisation orbitaire reste exceptionnelle. Cinquante-quatre cas seulement ont ete rapportes dans la litterature. Les auteu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b611faa91126147a75cebc60fd807fb
https://doi.org/10.1016/j.jfo.2010.11.006
https://doi.org/10.1016/j.jfo.2010.11.006