Correction: Status of alternative angiogenic pathways in glioblastoma resected under and after bevacizumab treatment.

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2024-10-01 DOI:10.1007/s10014-024-00485-w
Taketo Ezaki, Toshihide Tanaka, Ryota Tamura, Kentaro Ohara, Yohei Yamamoto, Jun Takei, Yukina Morimoto, Ryotaro Imai, Yuki Kuranari, Yasuharu Akasaki, Masahiro Toda, Yuichi Murayama, Keisuke Miyake, Hikaru Sasaki
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更正：贝伐单抗治疗下和治疗后切除的胶质母细胞瘤中替代血管生成途径的状况。
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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍： Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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Primary intracranial sarcoma associated with DICER1 mutant: a case report and preclinical investigation. Tectal glioma: clinical, radiological, and pathological features, and the importance of molecular analysis. Correction: Status of alternative angiogenic pathways in glioblastoma resected under and after bevacizumab treatment. MAPK pathway alterations in polymorphous low-grade neuroepithelial tumor of the young: diagnostic considerations. Comparative analyses of immune cells and alpha-smooth muscle actin-positive cells under the immunological microenvironment between with and without dense fibrosis in primary central nervous system lymphoma.
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