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Thomas Gasser

Showing results (141-150 of 476) with videos related to

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Frontiers in Neurology|January 2, 2023
Case Report: Deep brain stimulation improves tremor in <i>FGF-14</i> associated spinocerebellar ataxiaMoritz A Loeffler, Matthis Synofzik, Idil Cebi, et al.
Acta Neurochirurgica. Supplement|October 21, 2010
Intraoperative MRI and functional mappingThomas Gasser, Andrea Szelenyi, Christian Senft, et al.
Neuroscience Letters|May 3, 2006
Alpha2-macroglobulin, lipoprotein receptor-related protein and lipoprotein receptor-associated protein and the genetic risk for developing Alzheimer's diseaseCandan Depboylu, Frank Lohmüller, Yansheng Du, et al.
Nature|September 18, 2025
Global warming amplifies wildfire health burden and reshapes inequalityJunri Zhao, Bo Zheng, Philippe Ciais, et al.
Dementia and Geriatric Cognitive Disorders|January 24, 2004
An interleukin-6 promoter variant is not associated with an increased risk for Alzheimer's diseaseCandan Depboylu, Frank Lohmüller, Petra Gocke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
"Jerky" dystonia in children: spectrum of phenotypes and genetic testingFriedrich Asmus, Annette Langseth, Elaine Doherty, et al.
International Journal of Cancer|June 30, 2005
High-throughput tissue microarray analysis of CMYC amplificationin urinary bladder cancerBoriana Zaharieva, Ronald Simon, Christian Ruiz, et al.
Neurosurgery|September 18, 2008
Feasibility of Polestar N20, an ultra-low-field intraoperative magnetic resonance imaging system in resection control of pituitary macroadenomas: lessons learned from the first 40 casesRuediger Gerlach, Richard du Mesnil de Rochemont, Thomas Gasser, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 3, 2006
Vascular endothelial growth factor plasma levels are significantly elevated in patients with cerebral arteriovenous malformationsI Erol Sandalcioglu, Doreen Wende, Angelika Eggert, et al.
BMC Neurology|June 5, 2014
A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritanceMaik Engeholm, Julia Sekler, David C Schöndorf, et al.
Pageof 48

Showing results (141-150 of 476) with videos related to

Sort By:
Pageof 48
Frontiers in Neurology|January 2, 2023
Case Report: Deep brain stimulation improves tremor in <i>FGF-14</i> associated spinocerebellar ataxiaMoritz A Loeffler, Matthis Synofzik, Idil Cebi, et al.
Acta Neurochirurgica. Supplement|October 21, 2010
Intraoperative MRI and functional mappingThomas Gasser, Andrea Szelenyi, Christian Senft, et al.
Neuroscience Letters|May 3, 2006
Alpha2-macroglobulin, lipoprotein receptor-related protein and lipoprotein receptor-associated protein and the genetic risk for developing Alzheimer's diseaseCandan Depboylu, Frank Lohmüller, Yansheng Du, et al.
Nature|September 18, 2025
Global warming amplifies wildfire health burden and reshapes inequalityJunri Zhao, Bo Zheng, Philippe Ciais, et al.
Dementia and Geriatric Cognitive Disorders|January 24, 2004
An interleukin-6 promoter variant is not associated with an increased risk for Alzheimer's diseaseCandan Depboylu, Frank Lohmüller, Petra Gocke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
"Jerky" dystonia in children: spectrum of phenotypes and genetic testingFriedrich Asmus, Annette Langseth, Elaine Doherty, et al.
International Journal of Cancer|June 30, 2005
High-throughput tissue microarray analysis of CMYC amplificationin urinary bladder cancerBoriana Zaharieva, Ronald Simon, Christian Ruiz, et al.
Neurosurgery|September 18, 2008
Feasibility of Polestar N20, an ultra-low-field intraoperative magnetic resonance imaging system in resection control of pituitary macroadenomas: lessons learned from the first 40 casesRuediger Gerlach, Richard du Mesnil de Rochemont, Thomas Gasser, et al.
Cerebrovascular Diseases (Basel, Switzerland)|January 3, 2006
Vascular endothelial growth factor plasma levels are significantly elevated in patients with cerebral arteriovenous malformationsI Erol Sandalcioglu, Doreen Wende, Angelika Eggert, et al.
BMC Neurology|June 5, 2014
A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritanceMaik Engeholm, Julia Sekler, David C Schöndorf, et al.
Pageof 48