Douglas Galasko

ORCID: 0000-0001-6195-3241
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About
Contact & Profiles
Research Areas
  • Dementia and Cognitive Impairment Research
  • Alzheimer's disease research and treatments
  • Parkinson's Disease Mechanisms and Treatments
  • Neurological disorders and treatments
  • Amyotrophic Lateral Sclerosis Research
  • Neurological diseases and metabolism
  • Functional Brain Connectivity Studies
  • Cholinesterase and Neurodegenerative Diseases
  • Health Systems, Economic Evaluations, Quality of Life
  • Bioinformatics and Genomic Networks
  • Ginkgo biloba and Cashew Applications
  • Health, Environment, Cognitive Aging
  • Genetic Associations and Epidemiology
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Folate and B Vitamins Research
  • S100 Proteins and Annexins
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Computational Drug Discovery Methods
  • Nuclear Receptors and Signaling
  • Neurobiology of Language and Bilingualism
  • Epigenetics and DNA Methylation
  • Frailty in Older Adults
  • Neurological Disease Mechanisms and Treatments
  • MicroRNA in disease regulation
  • Memory and Neural Mechanisms

University of California, San Diego
2016-2025

Northwestern University
2024

Inha University
2024

VA San Diego Healthcare System
2015-2024

Indiana University – Purdue University Indianapolis
2020-2024

VIB-UAntwerp Center for Molecular Neurology
2024

University of Antwerp
2024

University of California, Los Angeles
1995-2024

University of California San Diego Medical Center
2005-2024

University of Iowa
2000-2024

Mild cognitive impairment is a transitional state between the changes of normal aging and early Alzheimer's disease.

10.1056/nejmoa050151 article EN New England Journal of Medicine 2005-04-14

Thirty-six clinically diagnosed and pathologically confirmed Alzheimer9s disease (AD) patients included 13 with cortical subcortical Lewy bodies (LBs). The LBs appeared to constitute a distinct neuropathologic clinical subset of AD, the body variant (LBV). LBV group showed gross pallor substantia nigra, greater neuron loss in locus ceruleus, innominata, lower neocortical ChAT levels, fewer midfrontal tangles than did pure AD group, along high incidence medial temporal lobe spongiform...

10.1212/wnl.40.1.1 article EN Neurology 1990-01-01

A Clinical Task Force, composed of clinical leaders from Alzheimer's Disease Centers (ADC), was convened by the National Institute on Aging to develop a uniform set assessment procedures characterize individuals with mild Alzheimer disease and cognitive impairment in comparison nondemented aging. The resulting Uniform Data Set (UDS) defines common observations be collected longitudinally ADC participants accordance standard methods. UDS implemented at all ADCs September 1, 2005. obtained are...

10.1097/01.wad.0000213865.09806.92 article EN Alzheimer Disease & Associated Disorders 2006-10-01

Abstract In this clinical study, the cerebrospinal fluid (CSF) level of a Novemberel form β‐amyloid peptide (Aβ) extending to position 42 (Aβ ) was determined in patients with Alzheimer's disease (AD) as well controls. addition measurement CSF Aβ levels, total peptides, microtubule‐associated protein τ, and apolipoprotein E (ApoE) genotype were also assessed. It is interesting that levels found be significantly lower AD relative controls, whereas not. has recently been shown preferentially...

10.1002/ana.410380413 article EN Annals of Neurology 1995-10-01

We compared two methods of diagnosing mild cognitive impairment (MCI): conventional Petersen/Winblad criteria as operationalized by the Alzheimer's Disease Neuroimaging Initiative (ADNI) and an actuarial neuropsychological method put forward Jak a

10.3233/jad-140276 article EN Journal of Alzheimer s Disease 2014-08-11

Biomarkers are urgently needed for the diagnosis and monitoring of disease progression in Parkinson’s disease. Both DJ-1 α-synuclein, two proteins critically involved pathogenesis, have been tested as biomarkers several recent studies with inconsistent results. These largely due to variation protein species detected by different antibodies, limited numbers patients some studies, or inadequate control important variables. In this study, nature α-synuclein human cerebrospinal fluid was studied...

10.1093/brain/awq008 article EN Brain 2010-02-15
Vivianna M. Van Deerlin Patrick Sleiman Maria Martinez‐Lage Alice Chen‐Plotkin Li-San Wang and 95 more Neill R. Graff‐Radford Dennis W. Dickson Rosa Rademakers Bradley F. Boeve Murray Grossman Steven E. Arnold David Mann Stuart Pickering‐Brown Harro Seelaar Peter Heutink John C. van Swieten Jill R. Murrell Bernardino Ghetti Salvatore Spina Jordan Grafman John R. Hodges Maria Grazia Spillantini Sid Gilman Andrew P. Lieberman Jeffrey Kaye Randall L. Woltjer Eileen H. Bigio Marsel Mesulam Safa Al‐Sarraj Claire Troakes Roger N. Rosenberg Charles L. White Isidró Ferrer Albert Lladó Manuela Neumann Hans A. Kretzschmar Christine M. Hulette Kathleen A. Welsh‐Bohmer Bruce L. Miller Ainhoa Alzualde Adolfo López de Munain Ann C. McKee Marla Gearing Allan I. Levey James J. Lah John Hardy Jonathan D. Rohrer Tammaryn Lashley Ian R. Mackenzie Howard Feldman Ronald L. Hamilton Steven T. DeKosky Julie van der Zee Samir Kumar‐Singh Christine Van Broeckhoven Richard Mayeux Jean Paul Vonsattel Juan C. Troncoso Jillian J. Kril John B. Kwok Glenda M. Halliday Thomas D. Bird Paul G. Ince Pamela J. Shaw Nigel J. Cairns John C. Morris Catriona McLean Charles DeCarli William G. Ellis Stefanie H. Freeman Matthew P. Frosch John H. Growdon Daniel P. Perl Mary Sano David A. Bennett Julie A. Schneider Thomas G. Beach Eric M. Reiman Bryan K. Woodruff Jeffrey L. Cummings Harry V. Vinters Carol A. Miller Helena C. Chui Irina Alafuzoff Päivi Hartikainen Danielle Seilhean Douglas Galasko Eliezer Masliah Carl W. Cotman MJ Tuñón Mònica Martínez David G. Muñoz Steven L. Carroll Daniel Marson Peter Riederer Nenad Bogdanović Daniela Berg Håkon Håkonarson John Q. Trojanowski Virginia M.‐Y. Lee

10.1038/ng.536 article EN Nature Genetics 2010-02-14
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