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David Fitzpatrick

Showing results (111-120 of 150) with videos related to

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Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine|March 22, 2019
Epidemiology of emergency ambulance service calls related to mental health problems and self harm: a national record linkage studyEdward A S Duncan, Catherine Best, Nadine Dougall, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|June 22, 2023
Lung Cancer in the Republic of IrelandRachel J Keogh, Martin P Barr, Anna Keogh, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearanceJill Clayton-Smith, Sarah Walters, Emma Hobson, et al.
Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.
Nature Neuroscience|March 3, 2017
Video-rate volumetric functional imaging of the brain at synaptic resolutionRongwen Lu, Wenzhi Sun, Yajie Liang, et al.
Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.
Nature Genetics|February 5, 2013
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomasMiriam J Smith, James O'Sullivan, Sanjeev S Bhaskar, et al.
Journal of Neurosurgery|February 7, 2025
Outcomes following stereotactic radiosurgery for high-grade brain arteriovenous malformations: a systematic review and meta-analysisImran Farhad, Adam Ridzuan-Allen, Saniya Ansari, et al.
Current Biology : CB|February 5, 2025
Eye saccades align optic flow with retinal specializations during object pursuit in freely moving ferretsDamian J Wallace, Kay-Michael Voit, Daniela Martin Machado, et al.
American Journal of Human Genetics|January 25, 2003
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathyKristien Verhoeven, Peter De Jonghe, Katrien Coen, et al.
Pageof 15

Showing results (111-120 of 150) with videos related to

Sort By:
Pageof 15
Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine|March 22, 2019
Epidemiology of emergency ambulance service calls related to mental health problems and self harm: a national record linkage studyEdward A S Duncan, Catherine Best, Nadine Dougall, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|June 22, 2023
Lung Cancer in the Republic of IrelandRachel J Keogh, Martin P Barr, Anna Keogh, et al.
European Journal of Human Genetics : EJHG|October 16, 2008
Xq28 duplication presenting with intestinal and bladder dysfunction and a distinctive facial appearanceJill Clayton-Smith, Sarah Walters, Emma Hobson, et al.
Human Genetics|January 11, 2007
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardationVera M Kalscheuer, David FitzPatrick, Niels Tommerup, et al.
Nature Neuroscience|March 3, 2017
Video-rate volumetric functional imaging of the brain at synaptic resolutionRongwen Lu, Wenzhi Sun, Yajie Liang, et al.
Nature Genetics|October 12, 2004
Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1BSandra Hanks, Kim Coleman, Sarah Reid, et al.
Nature Genetics|February 5, 2013
Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomasMiriam J Smith, James O'Sullivan, Sanjeev S Bhaskar, et al.
Journal of Neurosurgery|February 7, 2025
Outcomes following stereotactic radiosurgery for high-grade brain arteriovenous malformations: a systematic review and meta-analysisImran Farhad, Adam Ridzuan-Allen, Saniya Ansari, et al.
Current Biology : CB|February 5, 2025
Eye saccades align optic flow with retinal specializations during object pursuit in freely moving ferretsDamian J Wallace, Kay-Michael Voit, Daniela Martin Machado, et al.
American Journal of Human Genetics|January 25, 2003
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathyKristien Verhoeven, Peter De Jonghe, Katrien Coen, et al.
Pageof 15