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Rachael Scahill

Showing results (1-10 of 12) with videos related to

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Journal for Specialists in Pediatric Nursing : JSPN|July 8, 2015
Loss and rebuilding: A qualitative study of late diagnosis of cleft palateStephanie Tierney, Maria Blackhurst, Rachael Scahill, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2020
Diffusion imaging in Huntington's disease: comprehensive reviewCarlos Estevez-Fraga, Rachael Scahill, Geraint Rees, et al.
Neuroscience and Biobehavioral Reviews|February 5, 2013
Structural MRI in Huntington's disease and recommendations for its potential use in clinical trialsNellie Georgiou-Karistianis, Rachael Scahill, Sarah J Tabrizi, et al.
Neuroimage|October 19, 2004
Voxel-based morphometry detects patterns of atrophy that help differentiate progressive supranuclear palsy and Parkinson's diseaseShona Price, Dominic Paviour, Rachael Scahill, et al.
Journal of the International Neuropsychological Society : JINS|February 16, 2019
Apathy Associated With Impaired Recognition of Happy Facial Expressions in Huntington's DiseaseKatherine Osborne-Crowley, Sophie C Andrews, Izelle Labuschagne, et al.
Scientific Reports|March 11, 2018
Cerebrospinal fluid neurogranin and TREM2 in Huntington's diseaseLauren M Byrne, Filipe B Rodrigues, Eileanoir B Johnson, et al.
Brain : a Journal of Neurology|March 20, 2009
The clinical profile of right temporal lobe atrophyDennis Chan, Valerie Anderson, Yolande Pijnenburg, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|April 12, 2017
Embodied emotion impairment in Huntington's DiseaseIris Trinkler, Sévérine Devignevielle, Amal Achaibou, et al.
Dementia and Geriatric Cognitive Disorders|February 10, 2009
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutationJonathan D Rohrer, R Laila Ahsan, Adrian M Isaacs, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal for Specialists in Pediatric Nursing : JSPN|July 8, 2015
Loss and rebuilding: A qualitative study of late diagnosis of cleft palateStephanie Tierney, Maria Blackhurst, Rachael Scahill, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 9, 2020
Diffusion imaging in Huntington's disease: comprehensive reviewCarlos Estevez-Fraga, Rachael Scahill, Geraint Rees, et al.
Neuroscience and Biobehavioral Reviews|February 5, 2013
Structural MRI in Huntington's disease and recommendations for its potential use in clinical trialsNellie Georgiou-Karistianis, Rachael Scahill, Sarah J Tabrizi, et al.
Neuroimage|October 19, 2004
Voxel-based morphometry detects patterns of atrophy that help differentiate progressive supranuclear palsy and Parkinson's diseaseShona Price, Dominic Paviour, Rachael Scahill, et al.
Journal of the International Neuropsychological Society : JINS|February 16, 2019
Apathy Associated With Impaired Recognition of Happy Facial Expressions in Huntington's DiseaseKatherine Osborne-Crowley, Sophie C Andrews, Izelle Labuschagne, et al.
Scientific Reports|March 11, 2018
Cerebrospinal fluid neurogranin and TREM2 in Huntington's diseaseLauren M Byrne, Filipe B Rodrigues, Eileanoir B Johnson, et al.
Brain : a Journal of Neurology|March 20, 2009
The clinical profile of right temporal lobe atrophyDennis Chan, Valerie Anderson, Yolande Pijnenburg, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|April 12, 2017
Embodied emotion impairment in Huntington's DiseaseIris Trinkler, Sévérine Devignevielle, Amal Achaibou, et al.
Dementia and Geriatric Cognitive Disorders|February 10, 2009
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutationJonathan D Rohrer, R Laila Ahsan, Adrian M Isaacs, et al.
Brain : a Journal of Neurology|February 1, 2008
A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesJonathan Beck, Jonathan D Rohrer, Tracy Campbell, et al.
Pageof 2