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Neurology|November 1, 1982
Adult dystonic lipidosis: clinical, histologic, and biochemical findings of a neurovisceral storage diseaseW T Longstreth, J R Daven, D F Farrell, et al.Annals of Neurology|October 1, 1986
Widespread reduction of somatostatin-like immunoreactivity in the cerebral cortex in Alzheimer's diseaseM F Beal, M F Mazurek, C N Svendsen, et al.The Review of Scientific Instruments|December 31, 2022
A flexible neutron spectrometer concept with a new ultra-high field steady-state vertical-bore magnetB L Winn, C Broholm, M D Bird, et al.Archives of Neurology|September 1, 1990
Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?K Eto, S M Sumi, T D Bird, et al.Alzheimer Disease and Associated Disorders|January 1, 1987
The frequency of C4B variants of complement in familial and sporadic Alzheimer diseaseT D Bird, M Boehnke, J Anderson, et al.Annals of Neurology|November 1, 1986
A postmortem study of amino acid neurotransmitters in Alzheimer's diseaseD W Ellison, M F Beal, M F Mazurek, et al.Journal of Psychiatric Research|January 1, 1985
A corticosteroid/dopamine hypothesis for psychotic depression and related statesA F Schatzberg, A J Rothschild, P J Langlais, et al.Neurology|January 1, 1983
Lipomembranous polycystic osteodysplasia (brain, bone, and fat disease): a genetic cause of presenile dementiaT D Bird, R M Koerker, B J Leaird, et al.Neurology|April 1, 1996
Mapping of hereditary neuralgic amyotrophy (familial brachial plexus neuropathy) to distal chromosome 17qJ E Pellegrino, T R Rebbeck, M J Brown, et al.Microbial Ecology|March 17, 2001
The Responses of a Natural Bacterioplankton Community to Different Levels of Ultraviolet-B Radiation: A Food Web PerspectiveK. Chatila, S. Demers, B. Mostajir, et al.Pageof 873