Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Fatena Ajlouni"'
Autor:
Samer Salah, Maher A. Sughayer, Omar Jaber, Nebras Abu Abed, Fatena Ajlouni, Wisam Al Gargaz, Ramiz Abu Hijlih, Fawzi Abuhijla, Akram Al-Ibraheem, Farah Alul, Walid Naser
Publikováno v:
Case Reports in Oncological Medicine, Vol 2023 (2023)
Sarcoma with BCOR genetic alteration is an exceptionally rare and emerging subtype of sarcoma. It is categorized into two types: BCOR-related gene fusions such as BCOR::CCNB3 sarcomas and other BCOR-rearranged sarcoma and sarcomas with internal tande
Externí odkaz:
https://doaj.org/article/773a610f231b4444bd3ca68a028f039b
Autor:
Tamador Al-Shamaileh, Fatena Ajlouni, Rasha Deebajah, Iyad Sultan, Mohammad M. Saleem, Khalil Ghandour
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 46, Iss , Pp - (2019)
A 13-month-old female with sacro-coccygeal tumor type II by Altman, was proven by biopsy to be a malignant germ cell tumor. Serum tumor markers were normal. During neo-adjuvant chemotherapy visible tumor progression was confirmed radiologically and p
Externí odkaz:
https://doaj.org/article/f201908a3de549dfa55b889f343e37c8
Autor:
Mohammad M. Saleem, Tamador Al-Shamaileh, Fatena Ajlouni, Iyad Sultan, Khalil Ghandour, Rasha Deebajah
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 46, Iss, Pp-(2019)
A 13-month-old female with sacro-coccygeal tumor type II by Altman, was proven by biopsy to be a malignant germ cell tumor. Serum tumor markers were normal. During neo-adjuvant chemotherapy visible tumor progression was confirmed radiologically and p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e486c10a73c38cd125eec68552f2941f
https://doi.org/10.1016/j.epsc.2019.101194
https://doi.org/10.1016/j.epsc.2019.101194
Autor:
Main Masarweh, Usama Al-Jumaily, Maysa Al-Hussaini, Hasan Hashem, Maxim Al-Ashhab, Iyad Sultan, Khalil Ghandour, Fatena Ajlouni
Publikováno v:
Journal of Pediatric Surgery. 45:e13-e19
Teratoid Wilms tumor is an unusual variant of nephroblastoma in which heterologous tissue predominates. Typically, histopathologic examination shows a mixture of mature squamous and mucus-producing columnar epithelium and a prominent component of mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::163acc4292f6106109ea03af08d707e1
https://doi.org/10.1016/j.jpedsurg.2010.06.035
https://doi.org/10.1016/j.jpedsurg.2010.06.035
Autor:
Rasha Deebajeh, Maher A. Sughayer, Waleed Janem, Rula Y. Goussous, Hussam Haddad, Iyad Sultan, Fatena Ajlouni
Publikováno v:
Pediatric bloodcancer. 55(7)
Insulinomas are rare tumors with an estimated incidence of one per 250,000 person-years. Most insulinomas are benign with less than 10% demonstrating malignant behavior, the vast majority of which occur in adults. A systemic review of the literature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a4efb97fae8271229b729c741155b13
https://pubmed.ncbi.nlm.nih.gov/20860043
https://pubmed.ncbi.nlm.nih.gov/20860043