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A Churchyard

Showing results (11-20 of 25) with videos related to

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Journal of Medical Genetics|August 16, 2003
De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bonesM B Delatycki, A Danks, A Churchyard, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 28, 2014
Emotion perception and electrophysiological correlates in Huntington's diseaseR J Croft, F McKernan, M Gray, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2006
Tremor/ataxia syndrome and fragile X premutation: diagnostic caveatsD Z Loesch, L Litewka, A Churchyard, et al.
Chest|October 26, 1999
A multicenter study of grepafloxacin and clarithromycin in the treatment of patients with community-acquired pneumoniaS Moola, L Hagberg, G A Churchyard, et al.
The British Journal of Dermatology|May 15, 1998
Panniculitis in association with apomorphine infusionK M Acland, A Churchyard, C L Fletcher, et al.
BMJ (Clinical Research Ed.)|May 16, 1998
Investigation by Parkinson's Disease Research Group of United Kingdom into excess mortality seen with combined levodopa and selegiline treatment in patients with early, mild Parkinson's disease: further results of randomised trial and confidential inquiryY Ben-Shlomo, A Churchyard, J Head, et al.
Brain : a Journal of Neurology|June 27, 2000
Physiological, pharmacological and neurohormonal assessment of autonomic function in progressive supranuclear palsyJ Kimber, C J Mathias, A J Lees, et al.
Experimental Neurology|November 6, 2012
Prefrontal activity in Huntington's disease reflects cognitive and neuropsychiatric disturbances: the IMAGE-HD studyM A Gray, G F Egan, A Ando, et al.
Journal of Medical Genetics|December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.
Neuropsychologia|July 31, 2003
Hypometric primary saccades and increased variability in visually-guided saccades in Huntington's diseaseC T Winograd-Gurvich, N Georgiou-Karistianis, A Evans, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Journal of Medical Genetics|August 16, 2003
De novo germline PTEN mutation in a man with Lhermitte-Duclos disease which arose on the paternal chromosome and was transmitted to his child with polydactyly and Wormian bonesM B Delatycki, A Danks, A Churchyard, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 28, 2014
Emotion perception and electrophysiological correlates in Huntington's diseaseR J Croft, F McKernan, M Gray, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2006
Tremor/ataxia syndrome and fragile X premutation: diagnostic caveatsD Z Loesch, L Litewka, A Churchyard, et al.
Chest|October 26, 1999
A multicenter study of grepafloxacin and clarithromycin in the treatment of patients with community-acquired pneumoniaS Moola, L Hagberg, G A Churchyard, et al.
The British Journal of Dermatology|May 15, 1998
Panniculitis in association with apomorphine infusionK M Acland, A Churchyard, C L Fletcher, et al.
BMJ (Clinical Research Ed.)|May 16, 1998
Investigation by Parkinson's Disease Research Group of United Kingdom into excess mortality seen with combined levodopa and selegiline treatment in patients with early, mild Parkinson's disease: further results of randomised trial and confidential inquiryY Ben-Shlomo, A Churchyard, J Head, et al.
Brain : a Journal of Neurology|June 27, 2000
Physiological, pharmacological and neurohormonal assessment of autonomic function in progressive supranuclear palsyJ Kimber, C J Mathias, A J Lees, et al.
Experimental Neurology|November 6, 2012
Prefrontal activity in Huntington's disease reflects cognitive and neuropsychiatric disturbances: the IMAGE-HD studyM A Gray, G F Egan, A Ando, et al.
Journal of Medical Genetics|December 7, 2007
A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changesD Z Loesch, M Cook, L Litewka, et al.
Neuropsychologia|July 31, 2003
Hypometric primary saccades and increased variability in visually-guided saccades in Huntington's diseaseC T Winograd-Gurvich, N Georgiou-Karistianis, A Evans, et al.
Pageof 3