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Paritosh Pandey

Showing results (81-90 of 91) with videos related to

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Neurology India|November 15, 2016
Microsurgical treatment of distal anterior cerebral artery aneurysms: A 25 year institutional experienceDhaval Shukla, Dhananjaya I Bhat, Dwarkanath Srinivas, et al.
Journal of Neurosurgery. Pediatrics|March 21, 2008
Cerebellar abscesses in children: excision or aspiration?Paritosh Pandey, Srikantha Umesh, Dhananjaya Bhat, et al.
World Neurosurgery|March 6, 2013
The pterional and suprabrow approaches for aneurysm surgery: a systematic review of intraoperative rupture rates in 9488 aneurysmsVenkatesh S Madhugiri, Sudheer Ambekar, Paritosh Pandey, et al.
Cureus|September 8, 2025
Assessment of the Clinical Efficacy and Safety of Azithromycin in Patients With Moderate to Severe Upper Respiratory Tract Infections (URTIs): Insights From an Indian Real-World StudyHarihara Murthy, Pawan Singhal, Carlton Pereira, et al.
Pediatric Neurosurgery|September 7, 2011
Focal intradural brain infections in children: an analysis of management and outcomeVenkatesh S Madhugiri, B V Savitr Sastri, Umesh Srikantha, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 20, 2015
Lack of IDH1 mutation in astroblastomas suggests putative origin from ependymoglial cells?Unchagi Asha, Anita Mahadevan, Dhinakaran Sathiyabama, et al.
Journal of Neurosurgery|April 10, 2012
Multimodality management of Spetzler-Martin Grade III arteriovenous malformationsParitosh Pandey, Michael P Marks, Ciara D Harraher, et al.
Cancer Biology & Therapy|August 30, 2008
PBEF1/NAmPRTase/Visfatin: a potential malignant astrocytoma/glioblastoma serum marker with prognostic valueP Sreekanth Reddy, Srikantha Umesh, Balaram Thota, et al.
BMC Medical Genetics|May 1, 2015
Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variationManjunath Netravathi, Renu Kumari, Saketh Kapoor, et al.
Plos One|May 7, 2013
A fourteen gene GBM prognostic signature identifies association of immune response pathway and mesenchymal subtype with high risk groupArivazhagan Arimappamagan, Kumaravel Somasundaram, Kandavel Thennarasu, et al.
Pageof 10

Showing results (81-90 of 91) with videos related to

Sort By:
Pageof 10
Neurology India|November 15, 2016
Microsurgical treatment of distal anterior cerebral artery aneurysms: A 25 year institutional experienceDhaval Shukla, Dhananjaya I Bhat, Dwarkanath Srinivas, et al.
Journal of Neurosurgery. Pediatrics|March 21, 2008
Cerebellar abscesses in children: excision or aspiration?Paritosh Pandey, Srikantha Umesh, Dhananjaya Bhat, et al.
World Neurosurgery|March 6, 2013
The pterional and suprabrow approaches for aneurysm surgery: a systematic review of intraoperative rupture rates in 9488 aneurysmsVenkatesh S Madhugiri, Sudheer Ambekar, Paritosh Pandey, et al.
Cureus|September 8, 2025
Assessment of the Clinical Efficacy and Safety of Azithromycin in Patients With Moderate to Severe Upper Respiratory Tract Infections (URTIs): Insights From an Indian Real-World StudyHarihara Murthy, Pawan Singhal, Carlton Pereira, et al.
Pediatric Neurosurgery|September 7, 2011
Focal intradural brain infections in children: an analysis of management and outcomeVenkatesh S Madhugiri, B V Savitr Sastri, Umesh Srikantha, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|March 20, 2015
Lack of IDH1 mutation in astroblastomas suggests putative origin from ependymoglial cells?Unchagi Asha, Anita Mahadevan, Dhinakaran Sathiyabama, et al.
Journal of Neurosurgery|April 10, 2012
Multimodality management of Spetzler-Martin Grade III arteriovenous malformationsParitosh Pandey, Michael P Marks, Ciara D Harraher, et al.
Cancer Biology & Therapy|August 30, 2008
PBEF1/NAmPRTase/Visfatin: a potential malignant astrocytoma/glioblastoma serum marker with prognostic valueP Sreekanth Reddy, Srikantha Umesh, Balaram Thota, et al.
BMC Medical Genetics|May 1, 2015
Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variationManjunath Netravathi, Renu Kumari, Saketh Kapoor, et al.
Plos One|May 7, 2013
A fourteen gene GBM prognostic signature identifies association of immune response pathway and mesenchymal subtype with high risk groupArivazhagan Arimappamagan, Kumaravel Somasundaram, Kandavel Thennarasu, et al.
Pageof 10