Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Husam Bashir"'
Publikováno v:
Indian Journal of Vascular and Endovascular Surgery, Vol 8, Iss 2, Pp 187-189 (2021)
Stewart–Treves syndrome (STS) is a rare entity with a poor prognosis defined as an angiosarcoma appearing in a specific clinical setting, in 90% of cases in a context of breast neoplasia. Herein, we report a rare case of STS of the upper limb as a
Externí odkaz:
https://doaj.org/article/4f6c1d5a49334b5b801690be250ef8bb
Autor:
Aboleil‐Zoubi, Olfat, Gafni‐Amsalem, Chen, Peled‐Perets, Lilach, Mamluk, Efrat, Tamir, Liron, Hakrosh, Shadia, Kurtzman, Shoshana, Chervinsky, Elena, Aalimi, Ula, Husam, Bashir, Khayat, Morad, Baram‐Tsabari, Ayelet, Shalev, Stavit A.
Publikováno v:
Journal of Genetic Counseling; Jun2024, Vol. 33 Issue 3, p666-676, 11p
Akademický článek
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Autor:
Youssef Banana, Husam Bashir, Sara Boukabous, Intissar Haddiya, Yassamine Bentata, Abdellah Rezziki, Adnane Benzirar, Omar El Mahi
Publikováno v:
Annals of Medicine & Surgery. 85:485-487
Autor:
Eran Cohen‐Barak, Hagit Toledano‐Alhadef, Nada Danial‐Farran, Ido Livneh, Banan Mwassi, Maysa Hriesh, Fadia Zagairy, Chen Gafni‐Amsalem, Husam Bashir, Morad Khayat, Nassim Warrour, Osnat Sher, Daphna Marom, Sergey Postovsky, Tal Dujovny, Michael Ziv, Stavit A. Shalev
Publikováno v:
Experimental Dermatology. 31:775-780
Neurofibromatosis 1 (NF1) is caused by germline mutations in the NF1 gene and manifests as proliferation of various tissues, including plexiform neurofibromas. The plexiform neurofibroma phenotype varies from indolent to locally aggressive, suggestin
Autor:
Youssef Banana, Husam Bashir, Sara Boukabous, Abdellah Rezziki, Adnane Benzirar, Omar El Mahi
Publikováno v:
Annals of Medicine & Surgery. 76
Publikováno v:
Indian Journal of Vascular and Endovascular Surgery, Vol 8, Iss 2, Pp 187-189 (2021)
Stewart–Treves syndrome (STS) is a rare entity with a poor prognosis defined as an angiosarcoma appearing in a specific clinical setting, in 90% of cases in a context of breast neoplasia. Herein, we report a rare case of STS of the upper limb as a
Publikováno v:
Digestive Diseases and Sciences. 62:2095-2101
Data on inflammatory bowel disease (IBD) phenotypes among the Arab population in Israel or in the neighboring Arab countries is scarce. We aimed to assess differences in disease phenotype among Arab and Jewish children living in Israel. We performed
Autor:
Sarit Peleg, Yardena Tennenbaum-Rakover, Osama Tanous, Husam Bashir, Basel Badarneh, Firas Rinawi
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 108(1)
AIM Elevated levels of anti-tissue transglutaminase (anti-tTG) antibody may spontaneously normalise in children with newly diagnosed type 1 diabetes, even if they eat gluten. The prevalence of this phenomenon and predictors of a subsequent coeliac di