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Nooshin Zaresharifi

Explore the profile of Nooshin Zaresharifi including associated specialties, affiliations and a list of published articles. Areas
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Articles 13
Citations 17
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Recent Articles
1.
Zaresharifi N, Khalili A, Eftekhari B, Reihanian Z
Int J Surg Case Rep . 2025 Mar; 129:111094. PMID: 40058218
Introduction And Importance: Glioblastoma multiforme (GBM), a grade 4 astrocytoma, represents a predominant malignant primary tumor within the central nervous system (CNS) and is known for its dismal prognosis. While...
2.
Reihanian Z, Abbaspour E, Zaresharifi N, Karimzadhagh S, Mahmoudalinejad M, Sourati A, et al.
Cancer Rep (Hoboken) . 2024 Nov; 7(11):e70050. PMID: 39506810
Background: Glioblastoma multiforme (GBM) poses a significant health challenge as the most common primary malignancy of the adult central nervous system. Gender- and age-related differences in GBM influence prognosis and...
3.
Karimian P, Karimzadhagh S, Amirian B, Rafiee A, Shokrgozar L, Zaresharifi N
Int J Surg Case Rep . 2024 Oct; 124:110461. PMID: 39418989
Introduction: Ectopic pancreatic tissue (EPT), also known as Heterotopic pancreas (HP), is a rare congenital anomaly characterized by the presence of pancreatic tissue outside the primary organ. This report presents...
4.
Emamhadi M, Zaresharifi N, Reihanian Z, Khalili A, Ashoobi M, Noroozi Guilandehi S, et al.
Ann Med Surg (Lond) . 2024 Oct; 86(10):6241-6245. PMID: 39359754
Introduction And Importance: Primitive neuro-ectodermal tumor (PNET) is a highly aggressive tumor composed of small round blue cells, mostly developing in children and young adults. Being a member of Ewing's...
5.
Alijani B, Abbaspour E, Karimzadhagh S, Reihanian Z, Haghani Dogahe M, Jafari M, et al.
BMC Urol . 2024 Jun; 24(1):119. PMID: 38858693
Background: Wilms tumor (WT), also known as nephroblastoma, is rare in adults, accounting for merely 3% of all nephroblastomas or 0.2 cases per million individuals. Extrarenal Wilms tumor (ERWT) emerges...
6.
Alijani B, Karimzadhagh S, Abbaspour E, Reihanian Z, Haghani Dogahe M, Zaresharifi N
Int J Surg Case Rep . 2024 Feb; 116:109331. PMID: 38340621
Introduction: Spinal epidermoid tumors are exceptionally rare, comprising less than 1 % of all spinal tumors. True intramedullary epidermoid cysts (IECs) are even more infrequent, constituting only 0.8 % of...
7.
Zaresharifi N, Abbaspour E, Yousefzade-Chabok S, Reihanian Z, Karimian P, Karimzadhagh S
Int J Surg Case Rep . 2024 Jan; 115:109322. PMID: 38281381
Introduction And Importance: Medulloblastoma in adults is a rare and highly aggressive central nervous system (CNS) tumor, representing less than 1 % of all brain tumors. Supratentorial metastasis is uncommon,...
8.
Zaresharifi N, Karimzadhagh S, Reihanian Z, Jahanzad I, Ashoobi M
Ann Med Surg (Lond) . 2023 Dec; 85(12):6256-6261. PMID: 38098609
Introduction And Importance: Osteoblastoma (OB) is a rare benign bone tumor, representing less than 1% of all bone neoplasms. In contrast to the typical OB, a smaller subset known as...
9.
Zaresharifi N, Karimzadhagh S, Ebrahimian R, Reihanian Z, Abbaspour E, Karimian P, et al.
Ann Med Surg (Lond) . 2023 Dec; 85(12):6279-6284. PMID: 38098556
Introduction And Importance: Schwannomas, originating from Schwann cells surrounding nerve sheaths, tend to be slow-growing. Among these, giant ancient schwannomas are remarkable for their rare occurrence and their capacity for...
10.
Zaresharifi N, Khalili A, Eftekhari B, Layegh H
Clin Case Rep . 2023 Oct; 11(10):e7961. PMID: 37808579
Ectopic pancreatic tissue is a rare congenital abnormality defined as the abnormal location of pancreatic tissue outside the anatomical site of the pancreas without any anatomical or vascular connection to...