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Daniel Crooks

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Endocrine Journal|May 24, 2008
Lymphocytic hypophysitis occurring simultaneously with a functioning pituitary adenomaDaniel J Cuthbertson, Dave Ritchie, Daniel Crooks, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 24, 2006
Meningeal melanocytomaDonncha F O'Brien, Daniel Crooks, Conor Mallucci, et al.
British Journal of Cancer|April 22, 2016
Metastasis-inducing proteins are widely expressed in human brain metastases and associated with intracranial progression and radiation responseRasheed Zakaria, Angela Platt-Higgins, Nitika Rathi, et al.
The Journal of the Royal College of Physicians of Edinburgh|June 13, 2019
Steroid refractory giant cell arteritis with bilateral vertebral artery occlusion and middle cerebellar peduncle infarctionSarah Healy, Mark Simpson, William J Kitchen, et al.
Acta Neurochirurgica|August 17, 2016
The impact of MGMT methylation and IDH-1 mutation on long-term outcome for glioblastoma treated with chemoradiotherapyChristopher P Millward, Andrew R Brodbelt, Brian Haylock, et al.
Annals of Neurology|November 5, 2003
An English kindred with a novel recessive tauopathy and respiratory failureDavid J Nicholl, Michael A Greenstone, Carl E Clarke, et al.
Human Molecular Genetics|May 6, 2015
Identifying the biological pathways underlying human focal epilepsy: from complexity to coherence to centralityNasir Mirza, Richard Appleton, Sasha Burn, et al.
Epilepsia|July 17, 2016
An integrative in silico system for predicting dysregulated genes in the human epileptic focus: Application to SLC transportersNasir Mirza, Olga Vasieva, Richard Appleton, et al.
Pain|October 20, 2009
Absence of pain with hyperhidrosis: a new syndrome where vascular afferents may mediate cutaneous sensationDavid Bowsher, C Geoffrey Woods, Adeline K Nicholas, et al.
Annals of Neurology|October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defectKyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Endocrine Journal|May 24, 2008
Lymphocytic hypophysitis occurring simultaneously with a functioning pituitary adenomaDaniel J Cuthbertson, Dave Ritchie, Daniel Crooks, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|February 24, 2006
Meningeal melanocytomaDonncha F O'Brien, Daniel Crooks, Conor Mallucci, et al.
British Journal of Cancer|April 22, 2016
Metastasis-inducing proteins are widely expressed in human brain metastases and associated with intracranial progression and radiation responseRasheed Zakaria, Angela Platt-Higgins, Nitika Rathi, et al.
The Journal of the Royal College of Physicians of Edinburgh|June 13, 2019
Steroid refractory giant cell arteritis with bilateral vertebral artery occlusion and middle cerebellar peduncle infarctionSarah Healy, Mark Simpson, William J Kitchen, et al.
Acta Neurochirurgica|August 17, 2016
The impact of MGMT methylation and IDH-1 mutation on long-term outcome for glioblastoma treated with chemoradiotherapyChristopher P Millward, Andrew R Brodbelt, Brian Haylock, et al.
Annals of Neurology|November 5, 2003
An English kindred with a novel recessive tauopathy and respiratory failureDavid J Nicholl, Michael A Greenstone, Carl E Clarke, et al.
Human Molecular Genetics|May 6, 2015
Identifying the biological pathways underlying human focal epilepsy: from complexity to coherence to centralityNasir Mirza, Richard Appleton, Sasha Burn, et al.
Epilepsia|July 17, 2016
An integrative in silico system for predicting dysregulated genes in the human epileptic focus: Application to SLC transportersNasir Mirza, Olga Vasieva, Richard Appleton, et al.
Pain|October 20, 2009
Absence of pain with hyperhidrosis: a new syndrome where vascular afferents may mediate cutaneous sensationDavid Bowsher, C Geoffrey Woods, Adeline K Nicholas, et al.
Annals of Neurology|October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defectKyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
Pageof 2