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Neuroscience Letters|January 25, 2006
CHMP2B mutations are not a common cause of frontotemporal lobar degenerationAshley Cannon, Matthew Baker, Brad Boeve, et al.
Annals of Neurology|July 12, 2002
Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matterVictoria Zhukareva, David Mann, Stuart Pickering-Brown, et al.
Neurobiology of Aging|November 7, 2017
Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's diseaseSultan Chaudhury, Tulsi Patel, Imelda S Barber, et al.
Advances in Experimental Medicine and Biology|November 28, 2015
Impacts of Underwater Noise on Marine Vertebrates: Project Introduction and First ResultsAlexander Liebschner, Henrike Seibel, Jonas Teilmann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutationStuart Pickering-Brown, Matt Baker, Thomas Bird, et al.
Brain : a Journal of Neurology|September 4, 2016
Vascular cognitive impairment neuropathology guidelines (VCING): the contribution of cerebrovascular pathology to cognitive impairmentOlivia A Skrobot, Johannes Attems, Margaret Esiri, et al.
Neurobiology of Disease|February 15, 2008
Association study of the GAB2 gene with the risk of developing Alzheimer's diseaseJulien Chapuis, Didier Hannequin, Florence Pasquier, et al.
Plos One|November 13, 2010
Hearing loss in stranded odontocete dolphins and whalesDavid Mann, Mandy Hill-Cook, Charles Manire, et al.
Acta Neuropathologica|April 5, 2003
Selective reduction of soluble tau proteins in sporadic and familial frontotemporal dementias: an international follow-up studyVictoria Zhukareva, Sonali Sundarraj, David Mann, et al.
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