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Murat Gunel

Showing results (51-60 of 118) with videos related to

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Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.
Neuro-Oncology|April 29, 2021
Targeting the CSF1/CSF1R axis is a potential treatment strategy for malignant meningiomasJacky Yeung, Vesal Yaghoobi, Danielle Miyagishima, et al.
JCI Insight|May 17, 2016
PD-1 marks dysfunctional regulatory T cells in malignant gliomasDaniel E Lowther, Brittany A Goods, Liliana E Lucca, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Journal of Neurosurgery. Case Lessons|March 7, 2023
Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative caseChristopher S Hong, Neelan J Marianayagam, Saul F Morales-Valero, et al.
Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.
JAMA Network Open|February 16, 2024
APOE ε4 and Intracerebral Hemorrhage in Patients With Brain Arteriovenous MalformationDaniela Renedo, Cyprien A Rivier, Andrew B Koo, et al.
Journal of Neurosurgery. Pediatrics|January 20, 2018
Human genetics and molecular mechanisms of vein of Galen malformationDaniel Duran, Philipp Karschnia, Jonathan R Gaillard, et al.
American Journal of Human Genetics|March 12, 2013
Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalitiesFarid Radmanesh, Ahmet Okay Caglayan, Jennifer L Silhavy, et al.
Journal of the American Heart Association|April 7, 2025
Impact of Social Determinants of Health on Outcomes of Nontraumatic Subarachnoid HemorrhageDaniela Renedo, Cyprien A Rivier, Andrew Koo, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Neurogenetics|March 7, 2008
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish populationBeyhan Tüysüz, Fatih Bayrakli, Michael L DiLuna, et al.
Neuro-Oncology|April 29, 2021
Targeting the CSF1/CSF1R axis is a potential treatment strategy for malignant meningiomasJacky Yeung, Vesal Yaghoobi, Danielle Miyagishima, et al.
JCI Insight|May 17, 2016
PD-1 marks dysfunctional regulatory T cells in malignant gliomasDaniel E Lowther, Brittany A Goods, Liliana E Lucca, et al.
Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.
Journal of Neurosurgery. Case Lessons|March 7, 2023
Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative caseChristopher S Hong, Neelan J Marianayagam, Saul F Morales-Valero, et al.
Neurogenetics|January 19, 2010
Novel VLDLR microdeletion identified in two Turkish siblings with pachygyria and pontocerebellar atrophyLuis E Kolb, Zulfikar Arlier, Cengiz Yalcinkaya, et al.
JAMA Network Open|February 16, 2024
APOE ε4 and Intracerebral Hemorrhage in Patients With Brain Arteriovenous MalformationDaniela Renedo, Cyprien A Rivier, Andrew B Koo, et al.
Journal of Neurosurgery. Pediatrics|January 20, 2018
Human genetics and molecular mechanisms of vein of Galen malformationDaniel Duran, Philipp Karschnia, Jonathan R Gaillard, et al.
American Journal of Human Genetics|March 12, 2013
Mutations in LAMB1 cause cobblestone brain malformation without muscular or ocular abnormalitiesFarid Radmanesh, Ahmet Okay Caglayan, Jennifer L Silhavy, et al.
Journal of the American Heart Association|April 7, 2025
Impact of Social Determinants of Health on Outcomes of Nontraumatic Subarachnoid HemorrhageDaniela Renedo, Cyprien A Rivier, Andrew Koo, et al.
Pageof 12