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Progress in Hereditary Tauopathies: A Mutation in the Tau Gene (G389R) Causes a Pick Disease-like Syndrome.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 920, n. 1, p. 52, doi. 10.1111/j.1749-6632.2000.tb06905.x
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- Publication type:
- Article
TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.
- Published in:
- Movement Disorders, 2009, v. 24, n. 12, p. 1842, doi. 10.1002/mds.22697
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- Publication type:
- Article
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans.
- Published in:
- 2013
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- Publication type:
- journal article
Variants in the ATP-Binding Cassette Transporter (ABCA7), Apolipoprotein E ε4 and the Risk of Late-Onset Alzheimer Disease in African Americans.
- Published in:
- JAMA: Journal of the American Medical Association, 2013, v. 309, n. 14, p. 1483, doi. 10.1001/jama.2013.2973
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- Publication type:
- Article
A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data.
- Published in:
- Genome Medicine, 2020, v. 12, n. 1, p. 1, doi. 10.1186/s13073-020-0712-0
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- Publication type:
- Article
11C-PiB PET can underestimate brain amyloid-β burden when cotton wool plaques are numerous.
- Published in:
- 2022
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- Publication type:
- journal article
Mutation ∆K281 in MAPT causes Pick's disease.
- Published in:
- Acta Neuropathologica, 2023, v. 146, n. 2, p. 211, doi. 10.1007/s00401-023-02598-6
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- Publication type:
- Article
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.
- Published in:
- Acta Neuropathologica, 2007, v. 113, n. 4, p. 461, doi. 10.1007/s00401-006-0182-5
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- Publication type:
- Article
Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the α-synuclein gene.
- Published in:
- Acta Neuropathologica, 2005, v. 110, n. 3, p. 298, doi. 10.1007/s00401-005-1042-4
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- Publication type:
- Article
A novel mutation (G217D) in the Presenilin 1 gene (PSEN1) in a Japanese family: presenile dementia and parkinsonism are associated with cotton wool plaques in the cortex and striatum.
- Published in:
- Acta Neuropathologica, 2002, v. 104, n. 2, p. 155, doi. 10.1007/s00401-002-0536-6
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- Publication type:
- Article
In vivo and Postmortem Clinicoanatomical Correlations in Frontotemporal Dementia and Parkinsonism Linked to Chromosome 17.
- Published in:
- Neurodegenerative Diseases, 2008, v. 5, n. 3/4, p. 215, doi. 10.1159/000113706
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- Publication type:
- Article
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.
- Published in:
- Nature Genetics, 2010, v. 42, n. 3, p. 234, doi. 10.1038/ng.536
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- Publication type:
- Article
The Tau Tubulin Kinases TTBK1/2 Promote Accumulation of Pathological TDP-43.
- Published in:
- PLoS Genetics, 2014, v. 10, n. 12, p. 1, doi. 10.1371/journal.pgen.1004803
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- Publication type:
- Article
The broader phenotypic spectrum of congenital caudal abnormalities associated with mutations in the caudal type homeobox 2 gene.
- Published in:
- Clinical Genetics, 2022, v. 101, n. 2, p. 183, doi. 10.1111/cge.14076
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- Publication type:
- Article
CONTRIBUTION OF THE NEUROPATHOLOGY LABORATORY AT INDIANA UNIVERSITY TO THE DECIPHERING OF DOMINANTLY INHERITED DEMENTIAS: 1976-2016.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P744, doi. 10.1016/j.jalz.2016.06.1553
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- Publication type:
- Article
NEUROPATHOLOGY OF FAMILIAL ALZHEIMER'S DISEASE ASSOCIATED WITH A PRESENILIN 1 A396T MUTATION REVEALS THE COEXISTENCE OF Aβ, TAU, AND A-SYNUCLEIN PROTEINOPATHIES.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P562, doi. 10.1016/j.jalz.2016.06.1099
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- Publication type:
- Article
NEURONAL INTRACYTOPLASMIC PRP DEPOSITS IN DOMINANTLY INHERITED CREUTZFELDT-JAKOB DISEASE ASSOCIATED WITH THE PRNP E200K-129V HAPLOTYPE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, p. P1116, doi. 10.1016/j.jalz.2016.06.2320
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- Publication type:
- Article
Dementia incidence declined in African-Americans but not in Yoruba.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2016, v. 12, n. 3, p. 244, doi. 10.1016/j.jalz.2015.06.1894
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- Publication type:
- Article
Glucose hypometabolism in gerstmann–sträussler–scheinker patients with the F198S mutation.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P530, doi. 10.1016/j.jalz.2015.06.662
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- Publication type:
- Article
Frontotemporal dementia and parkinsonism linked to chromosome 17 granulin: Clinical and pathologic study of a patient from a new pedigree.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P768, doi. 10.1016/j.jalz.2015.06.1713
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- Publication type:
- Article
Glucose hypometabolism in gerstmann–sträussler–scheinker patients with the F198S mutation.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P43, doi. 10.1016/j.jalz.2015.06.076
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- Publication type:
- Article
Multiple proteinopathies underlying atypical dementia.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P372, doi. 10.1016/j.jalz.2015.06.283
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- Publication type:
- Article
Genome-wide association of plasma homocysteine in the indianapolis-ibadan dementia study cohort.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P623, doi. 10.1016/j.jalz.2015.06.877
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- Publication type:
- Article
Neuropathologic characterization of cerebral β-amyloid angiopathy in familial cerebral hemorrhage.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2015, v. 11, n. 7, p. P431, doi. 10.1016/j.jalz.2015.06.412
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- Publication type:
- Article
Early onset and rapid course of Alzheimer disease associated with the I143T PSEN1 mutation.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P629, doi. 10.1016/j.jalz.2014.05.1095
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- Publication type:
- Article
Cognition and brain structure in Gerstmann-Straussler-Scheinker disease (PRNP F198S)
- Published in:
- 2010
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- Publication type:
- Abstract
Leisure activities and cognitive decline in a rural elderly Chinese cohort
- Published in:
- 2010
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- Publication type:
- Abstract
Novel TARDBP mutation associated with frontotemporal dementia and movement disorder but not motor neuron disease
- Published in:
- 2009
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- Publication type:
- Abstract
Prevalence rates for dementia and Alzheimer's disease in African Americans: 1992 versus 2001
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2009, v. 5, n. 3, p. 227, doi. 10.1016/j.jalz.2009.01.026
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- Publication type:
- Article
P4-121: Twelve year trajectories of cognitive decline in elderly African Americans
- Published in:
- 2008
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- Publication type:
- Abstract
P4-072: Selenium levels and cognitive decline in a rural elderly Chinese cohort
- Published in:
- 2008
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- Publication type:
- Abstract
P3-221: Familial Alzheimer's disease associated with the V717L amyloid precursor protein gene mutation: Neuropathological characterization
- Published in:
- 2008
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- Publication type:
- Abstract
P2-205: Neuropathologic and genetic characterization of frontotemporal lobar degeneration with ubiquitin- and/or TDP-43-positive inclusions: A large series
- Published in:
- 2008
- By:
- Publication type:
- Abstract
O4-05-06: Prevalence rates for demenita and Alzheimer's disease in elderly African Americans in Indianapolis: 1992 vs 2001
- Published in:
- 2008
- By:
- Publication type:
- Abstract
O2-05-03: Inclusion body myopathy with paget disease of the bone and frontotemporal dementia: New families, a novel mutation, and a new clinical presentation
- Published in:
- 2008
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- Publication type:
- Abstract
P4-109: Clinical symptoms and brainstem pathology in FTDP-17 associated with the EXON 10 +3 intronic Tau mutation
- Published in:
- 2006
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- Publication type:
- Abstract
P3-156: Early onset frontotemporal dementia and parkinsonism associated with the G335S Tau mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P4-109: Clinical symptoms and brainstem pathology in FTDP-17 associated with the EXON 10 +3 intronic Tau mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-156: Early onset frontotemporal dementia and parkinsonism associated with the G335S Tau mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Late Life Leisure Activities and Risk of Cognitive Decline.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2013, v. 68, n. 2, p. 205, doi. 10.1093/gerona/gls153
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- Publication type:
- Article
Trace Element Levels and Cognitive Function in Rural Elderly Chinese.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2008, v. 63, n. 6, p. 635, doi. 10.1093/gerona/63.6.635
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- Publication type:
- Article
Correlates of depressive symptoms in rural elderly Chinese.
- Published in:
- International Journal of Geriatric Psychiatry, 2009, v. 24, n. 12, p. 1358, doi. 10.1002/gps.2271
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- Publication type:
- Article
Hypertension and Cognitive Decline in Rural Elderly Chinese.
- Published in:
- Journal of the American Geriatrics Society, 2009, v. 57, n. 6, p. 1051, doi. 10.1111/j.1532-5415.2009.02267.x
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- Publication type:
- Article
Selenium level and depressive symptoms in a rural elderly Chinese cohort.
- Published in:
- BMC Psychiatry, 2012, v. 12, n. 1, p. 72, doi. 10.1186/1471-244X-12-72
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- Publication type:
- Article
Selenium Level and Cognitive Function in Rural Elderly Chinese.
- Published in:
- American Journal of Epidemiology, 2007, v. 165, n. 8, p. 955, doi. 10.1093/aje/kwk073
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- Publication type:
- Article
Selenium level is associated with apoE ϵ4 in rural elderly Chinese.
- Published in:
- Public Health Nutrition, 2009, v. 12, n. 12, p. 2371, doi. 10.1017/S1368980009005102
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- Publication type:
- Article
Detection of tau in Gerstmann-Sträussler-Scheinker disease (PRNP F198S) by [<sup>18</sup>F]Flortaucipir PET.
- Published in:
- Acta Neuropathologica Communications, 2018, v. 6, n. 1, p. N.PAG, doi. 10.1186/s40478-018-0608-z
- By:
- Publication type:
- Article
Encephalopathy with Neuroserpin Inclusion Bodies Presenting as Progressive Myoclonus Epilepsy and Associated with a Novel Mutation in the Proteinase Inhibitor 12 Gene.
- Published in:
- 2011
- By:
- Publication type:
- Other
PET of Brain Prion Protein Amyloid in Gerstmann–Sträussler–Scheinker Disease.
- Published in:
- Brain Pathology, 2010, v. 20, n. 2, p. 419, doi. 10.1111/j.1750-3639.2009.00306.x
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- Publication type:
- Article
Early-onset Dementia with Lewy Bodies.
- Published in:
- Brain Pathology, 2004, v. 14, n. 2, p. 137, doi. 10.1111/j.1750-3639.2004.tb00046.x
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- Publication type:
- Article