Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Khalid Alhajri"'
Publikováno v:
BMC Surgery, Vol 22, Iss 1, Pp 1-4 (2022)
Abstract Background Isolated iliac artery aneurysms are rare and difficult to diagnose. It is more common in males. It can be asymptomatic at diagnosis or can present with frank rupture, or symptoms caused by compression on nearby organs. Case presen
Externí odkaz:
https://doaj.org/article/1c8ff2916397441f9abe7fc7d3d2e034
Publikováno v:
Cureus.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ae84511f321174bd3d53b32a417a7c
https://doi.org/10.7759/cureus.35335
https://doi.org/10.7759/cureus.35335
Complementary and alternative medicine among cancer patients and its complications: local experience
Autor:
Ali Al-Amri, Rashed Alzahrani, Khalid Alhajri, Saleh Alqarzea, Faisal Alzahrani, Shams Alturky
Publikováno v:
International Journal of Medicine in Developing Countries. :2103-2107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15ae2d57790b24d8f839bd44dd65d858
https://doi.org/10.24911/ijmdc.51-1634153885
https://doi.org/10.24911/ijmdc.51-1634153885
Autor:
Anand Kumar Mishra, Amit Agarwal, Rajeev Parameswaran, Soe Tin, Ranil Fernando, Khalid Alhajri, Ali Korairi, Marya Al Suhaibani, Özer Makay
Publikováno v:
Endocrine Surgery ISBN: 9780429197338
[No abstract available]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95f4891fe256ec28c8695e4ad7a4ddd8
https://doi.org/10.1201/9780429197338-21
https://doi.org/10.1201/9780429197338-21
Autor:
Ashwag Alharbi, Bashayer Algarzaei, Rema Alrashed, Khalid Alhajri, Abdullah Alghamdi, Eyad Alkharashi, Hussam Bin Yousef, Khalid Alzoman
Publikováno v:
International Journal of Surgery Open. 48:100566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9403edc566d6bf9ecf7f0056aebd24b
https://doi.org/10.1016/j.ijso.2022.100566
https://doi.org/10.1016/j.ijso.2022.100566
Publikováno v:
Journal of the Endocrine Society
Background: Pheochromocytoma is a rare neuroendocrine tumour arising from chromaffin cells of the adrenal medulla that produce catecholamines and their metabolites. It accounts for up to 5-9% of adrenal incidentalomas (AI). Lack of hemodynamic featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83178f0861c0a6eff6cf4b99cbe7d9c8
http://europepmc.org/articles/PMC6550937
http://europepmc.org/articles/PMC6550937
Publikováno v:
Case Reports. 2011:bcr1220103591-bcr1220103591
The development of disseminated (miliary) abdominal tuberculosis (TB) in patients following operations which affect their immunity, such as laparoscopic gastric bypass, is rare. The authors report the case of middle aged woman, who a few months after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bedf8436eacb6dd7f35fd43ced780b49
https://doi.org/10.1136/bcr.12.2010.3591
https://doi.org/10.1136/bcr.12.2010.3591
Publikováno v:
Case Reports. 2011:bcr1220103604-bcr1220103604
Adrenal haemangioma is a rare, benign, non-functioning neoplasm. Haemangiomas are tumours mainly affecting the liver. In 1955, Johnson and Jeppesen described the first adrenal cavernous haemangioma. Here the authors report a large adrenal haemangioma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1362f52af20489493c39bacc544b8050
https://doi.org/10.1136/bcr.12.2010.3604
https://doi.org/10.1136/bcr.12.2010.3604