Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Susan Andalibi"'
Autor:
Hamid Nasrollahi, Susan Andalibi, Mansour Ansari, Maral Mokhtari, Ehsan Mohammad Hosseini, Mina Foroughi, Arman Sourani
Publikováno v:
Clinical Case Reports, Vol 12, Iss 6, Pp n/a-n/a (2024)
Key Clinical Message Intracranial RDD is rare medical event mimicking different diagnoses. Although the surgical resection is the best treatment option, but radiation therapy can also achieves long‐term suboptimal outcomes. Abstract An 83‐year‐
Externí odkaz:
https://doaj.org/article/81814184bf324cdeb4bfeebed7127b9d
Publikováno v:
Middle East Journal of Cancer, Vol 14, Iss 2, Pp 270-277 (2023)
Background: Cognitive impairment is one of the common problems in patients undergoing radiotherapy, but there is no way to prevent it until this time. The aim of this study was to determine the effect of memantine on the prevention of cognitive impai
Externí odkaz:
https://doaj.org/article/8b68655463c841258aa54cd56c0b1da3
Autor:
Ehsan Mohammadhosseini, Bahram Aminmansour, Susan Andalibi, Maryam Derakhshan, Fataneh Farokhpour
Publikováno v:
Iranian Journal of Neurosurgery, Vol 5, Iss 1, Pp 43-50 (2019)
Background and Aim: Primary central nervous system lymphoma (PCNSL) is a rare cancer confined to the brain, spinal cord, leptomeninges and eyes. The origin of this type of lymphoma is often type B lymphocytes, and because the central nervous system (
Externí odkaz:
https://doaj.org/article/3416442666964901acd3c2a23cb9c054
Autor:
Susan Andalibi, Bahram Aminmansour, Maryam Derakhshan, Ehsan Mohammadhosseini, Fataneh Farokhpour
Publikováno v:
Iranian Journal of Neurosurgery, Vol 5, Iss 1, Pp 43-50 (2019)
Background and Aim: Primary central nervous system lymphoma (PCNSL) is a rare cancer confined to the brain, spinal cord, leptomeninges and eyes. The origin of this type of lymphoma is often type B lymphocytes, and because the central nervous system (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6f2ae1554aad892e424cc40e784164d
https://doi.org/10.32598/irjns.5.1.43
https://doi.org/10.32598/irjns.5.1.43