A
Ashish Suri
Researcher at All India Institute of Medical Sciences
Publications - 300
Citations - 5286
Ashish Suri is an academic researcher from All India Institute of Medical Sciences. The author has contributed to research in topics: Medicine & Aneurysm. The author has an hindex of 34, co-authored 267 publications receiving 4372 citations. Previous affiliations of Ashish Suri include Indian Institute of Technology Delhi & Millennium Pharmaceuticals.
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Targeted therapy for high-grade glioma with the TGF-β2 inhibitor trabedersen: results of a randomized and controlled phase IIb study
Ulrich Bogdahn,Peter Hau,G. Stockhammer,N. K. Venkataramana,Ashok Kumar Mahapatra,Ashish Suri,A. Balasubramaniam,Sreejayan Nair,V. Oliushine,V. E. Parfenov,I. E. Poverennova,M. Zaaroor,P. Jachimczak,Stephan Ludwig,S. Schmaus,H. Heinrichs,Karl-Hermann Schlingensiepen +16 more
TL;DR: In this article, the authors evaluated the efficacy and safety of trabedersen (AP 12009) administered intratumorally by convection-enhanced delivery compared with standard chemotherapy in patients with recurrent/refractory high-grade glioma.
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Effect of intramedullary signal changes on the surgical outcome of patients with cervical spondylotic myelopathy.
TL;DR: The presence of intramedullary signal changes on T1- as well as T2-weighted sequences on MRI in patients with cervical spondylotic myelopathy indicates a poor prognosis, however, the T2 signal intensity changes reflect a broad spectrum of spinal cord reparative potentials.
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Comparative study of IDH1 mutations in gliomas by immunohistochemistry and DNA sequencing.
Shipra Agarwal,Mehar Chand Sharma,Prerana Jha,Pankaj Pathak,Vaishali Suri,Chitra Sarkar,Kunzang Chosdol,Ashish Suri,Shashank S. Kale,Ashok Kumar Mahapatra,Pankaj Jha +10 more
TL;DR: IHC is an easy and quick method of detecting IDH1-R132H mutations, but there may be some discrepancies between IHC and DNA sequencing.
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Pediatric glioblastomas: A histopathological and molecular genetic study
Vaishali Suri,Prasenjit Das,Ayushi Jain,Mehar Chand Sharma,Sachin A Borkar,Ashish Suri,Deepak Gupta,Chitra Sarkar +7 more
TL;DR: In pediatric de novo/primary GBMs, deletion of PTEN and EGFR amplification are rare, while p53 alterations are more frequent compared to primary adultGBMs, suggesting that pediatric malignant gliomas are distinctly different from adult GBMs.
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Anterior encephaloceles: a study of 92 cases.
TL;DR: Fontoethmoidal encephaloceles are the commonest type, followed by the nasopharyngeal and orbital type, and nasoethmoid is the common most common type among patients with significant hypertelorism and orbital deformities.